| Year |
Citation |
Score |
| 2023 |
Aleknonytė-Resch M, Trinh J, Leonard H, Delcambre S, Leitão E, Lai D, Smajić S, Orr-Urtreger A, Thaler A, Blauwendraat C, Sharma A, Makarious MB, Kim JJ, Lake J, Rahmati P, ... ... Foroud T, et al. Genome-wide case-only analysis of gene-gene interactions with known Parkinson's disease risk variants reveals link between LRRK2 and SYT10. Npj Parkinson's Disease. 9: 102. PMID 37386035 DOI: 10.1038/s41531-023-00550-9 |
0.317 |
|
| 2022 |
Straniero L, Rimoldi V, Monfrini E, Bonvegna S, Melistaccio G, Lake J, Soldà G, Aureli M, Keagle P, Foroud T, Landers JE, Blauwendraat C, Zecchinelli A, Cilia R, Di Fonzo A, et al. Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 35262230 DOI: 10.1002/mds.28987 |
0.306 |
|
| 2020 |
Alcalay RN, Wolf P, Chiang MSR, Helesicova K, Zhang XK, Merchant K, Hutten SJ, Scherzer C, Caspell-Garcia C, Blauwendraat C, Foroud T, Nudelman K, Gan-Or Z, Simuni T, Chahine LM, et al. Longitudinal Measurements of Glucocerebrosidase activity in Parkinson's patients. Annals of Clinical and Translational Neurology. PMID 32888397 DOI: 10.1002/Acn3.51164 |
0.344 |
|
| 2020 |
Schwantes-An TH, Darlay R, Mathurin P, Masson S, Liangpunsakul S, Mueller S, Aithal GP, Eyer F, Gleeson D, Thompson A, Muellhaupt B, Stickel F, Soyka M, Goldman D, Liang T, ... ... Foroud TM, et al. Genome-wide association study and meta-analysis on alcohol-related liver cirrhosis identifies novel genetic risk factors. Hepatology (Baltimore, Md.). PMID 32853455 DOI: 10.1002/Hep.31535 |
0.302 |
|
| 2020 |
Nho K, Nudelman K, Allen M, Hodges A, Kim S, Risacher SL, Apostolova LG, Lin K, Lunnon K, Wang X, Burgess JD, Ertekin-Taner N, Petersen RC, Wang L, Qi Z, ... ... Foroud T, et al. Genome-wide transcriptome analysis identifies novel dysregulated genes implicated in Alzheimer's pathology. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 32755048 DOI: 10.1002/Alz.12092 |
0.355 |
|
| 2020 |
Lai D, Kapoor M, Wetherill L, Schwandt M, Ramchandani VA, Goldman D, Chao M, Almasy L, Bucholz K, Hart RP, Kamarajan C, Meyers JL, Nurnberger JI, Tischfield J, Edenberg HJ, ... ... Foroud T, et al. Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32652861 DOI: 10.1002/Ajmg.B.32805 |
0.357 |
|
| 2020 |
Irwin DJ, Felder J, Coffey CS, Caspell-Garcia C, Kang JH, Simuni T, Foroud T, Toga AW, Tanner CM, Kieburtz K, Chahine LM, Reimer A, Hutten S, Weintraub D, Mollenhauer B, et al. Evolution of Alzheimer's Disease Cerebrospinal Fluid Biomarkers in Early Parkinson's Disease. Annals of Neurology. PMID 32542885 DOI: 10.1002/Ana.25811 |
0.337 |
|
| 2020 |
Meyers JL, Zhang J, Chorlian DB, Pandey AK, Kamarajan C, Wang JC, Wetherill L, Lai D, Chao M, Chan G, Kinreich S, Kapoor M, Bertelsen S, McClintick J, Bauer L, ... ... Foroud T, et al. A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior. Molecular Psychiatry. PMID 32433515 DOI: 10.1038/S41380-020-0777-6 |
0.388 |
|
| 2020 |
Simuni T, Brumm MC, Uribe L, Caspell-Garcia C, Coffey CS, Siderowf A, Alcalay R, Trojanowski JQ, Shaw LM, Seibyl J, Singleton A, Toga AW, Galasko D, Foroud T, Nudelman K, et al. Clinical and Dopamine Transporter Imaging Characteristics of Leucine- Rich Repeat Kinase 2 (LRRK2) and Glucosylceramidase Beta (GBA) Parkinson's Disease Participants in the Parkinson's Progression Markers Initiative: A Cross-Sectional Study. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32073681 DOI: 10.1002/Mds.27989 |
0.311 |
|
| 2020 |
Reiman EM, Arboleda-Velasquez JF, Quiroz YT, Huentelman MJ, Beach TG, Caselli RJ, Chen Y, Su Y, Myers AJ, Hardy J, Paul Vonsattel J, Younkin SG, Bennett DA, De Jager PL, Larson EB, ... ... Foroud T, et al. Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study. Nature Communications. 11: 667. PMID 32015339 DOI: 10.1038/S41467-019-14279-8 |
0.318 |
|
| 2020 |
Ramos EM, Dokuru DR, Van Berlo V, Wojta K, Wang Q, Huang AY, Deverasetty S, Qin Y, van Blitterswijk M, Jackson J, Appleby B, Bordelon Y, Brannelly P, Brushaber DE, Dickerson B, ... ... Foroud T, et al. Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 16: 118-130. PMID 31914217 DOI: 10.1002/Alz.12011 |
0.307 |
|
| 2019 |
Simuni T, Uribe L, Cho HR, Caspell-Garcia C, Coffey CS, Siderowf A, Trojanowski JQ, Shaw LM, Seibyl J, Singleton A, Toga AW, Galasko D, Foroud T, Tosun D, Poston K, et al. Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study. The Lancet. Neurology. PMID 31678032 DOI: 10.1016/S1474-4422(19)30319-9 |
0.342 |
|
| 2019 |
Wetherill L, Lai D, Johnson EC, Anokhin A, Bauer L, Bucholz KK, Dick DM, Hariri AR, Hesselbrock V, Kamarajan C, Kramer J, Kuperman S, Meyers JL, Nurnberger JI, Schuckit M, ... ... Foroud T, et al. ERRATUM: Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans. Genes, Brain, and Behavior. 18: e12608. PMID 31667958 DOI: 10.1111/Gbb.12608 |
0.325 |
|
| 2019 |
Meyers JL, Salvatore JE, Aliev F, Johnson EC, McCutcheon VV, Su J, Kuo SI, Lai D, Wetherill L, Wang JC, Chan G, Hesselbrock V, Foroud T, Bucholz KK, Edenberg HJ, et al. Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance. Translational Psychiatry. 9: 269. PMID 31636251 DOI: 10.1038/S41398-019-0598-Z |
0.334 |
|
| 2019 |
Meyers JL, Chorlian DB, Johnson EC, Pandey AK, Kamarajan C, Salvatore JE, Aliev F, Subbie-Saenz de Viteri S, Zhang J, Chao M, Kapoor M, Hesselbrock V, Kramer J, Kuperman S, Nurnberger J, ... ... Foroud T, et al. Association of Polygenic Liability for Alcohol Dependence and EEG Connectivity in Adolescence and Young Adulthood. Brain Sciences. 9. PMID 31627376 DOI: 10.3390/Brainsci9100280 |
0.354 |
|
| 2019 |
Rao X, Thapa KS, Chen AB, Lin H, Gao H, Reiter JL, Hargreaves KA, Ipe J, Lai D, Xuei X, Wang Y, Gu H, Kapoor M, Farris SP, Tischfield J, ... Foroud T, et al. Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders. Molecular Psychiatry. PMID 31477794 DOI: 10.1038/S41380-019-0508-Z |
0.385 |
|
| 2019 |
Agalliu I, Ortega RA, Luciano MS, Mirelman A, Pont-Sunyer C, Brockmann K, Vilas D, Tolosa E, Berg D, Warø B, Glickman A, Raymond D, Inzelberg R, Ruiz-Martinez J, Mondragon E, ... ... Foroud T, et al. Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 31348549 DOI: 10.1002/Mds.27807 |
0.351 |
|
| 2019 |
Lai D, Wetherill L, Kapoor M, Johnson EC, Schwandt M, Ramchandani VA, Goldman D, Joslyn G, Rao X, Liu Y, Farris S, Mayfield RD, Dick D, Hesselbrock V, Kramer J, ... ... Foroud T, et al. Genome-wide association studies of the self-rating of effects of ethanol (SRE). Addiction Biology. e12800. PMID 31270906 DOI: 10.1111/Adb.12800 |
0.37 |
|
| 2019 |
Wetherill L, Lai D, Johnson EC, Anokhin A, Bauer L, Bucholz KK, Dick DM, Hariri AR, Hesselbrock V, Kamarajan C, Kramer J, Kuperman S, Meyers JL, Nurnberger JI, Schuckit M, ... ... Foroud T, et al. Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans. Genes, Brain, and Behavior. e12580. PMID 31099175 DOI: 10.1111/Gbb.12580 |
0.401 |
|
| 2019 |
Lai D, Wetherill L, Bertelsen S, Carey CE, Kamarajan C, Kapoor M, Meyers JL, Anokhin AP, Bennett DA, Bucholz KK, Chang KK, De Jager PL, Dick DM, Hesselbrock V, Kramer J, ... ... Foroud T, et al. Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Genes, Brain, and Behavior. PMID 31090166 DOI: 10.1111/Gbb.12579 |
0.379 |
|
| 2019 |
Kapoor M, Wang JC, Farris SP, Liu Y, McClintick J, Gupta I, Meyers JL, Bertelsen S, Chao M, Nurnberger J, Tischfield J, Harari O, Zeran L, Hesselbrock V, Bauer L, ... ... Foroud T, et al. Analysis of whole genome-transcriptomic organization in brain to identify genes associated with alcoholism. Translational Psychiatry. 9: 89. PMID 30765688 DOI: 10.1038/S41398-019-0384-Y |
0.339 |
|
| 2019 |
Salvatore J, Barr P, Kuo SI, Su J, Almasy L, Brooks A, Bucholz K, Chao M, Edenberg H, Foroud T, Hesselbrock V, Kramer J, Nurnberger J, Kuperman S, Dick D. Sa137Social Genetics Effects On Alcohol Dependence In Marital Dyads European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.359 |
0.315 |
|
| 2019 |
Edenberg H, Goate A, Liu Y, Kapoor M, Chan G, Wetherill L, Lai D, McClintick J, Hesselbrock V, Kramer J, Kuperman S, Porjesz B, Tischfield J, Foroud T. Exome Sequencing and Genomic Studies To Better Understand Alcohol Dependence European Neuropsychopharmacology. 29: S731. DOI: 10.1016/J.Euroneuro.2017.06.054 |
0.406 |
|
| 2018 |
Brazel DM, Jiang Y, Hughey JM, Turcot V, Zhan X, Gong J, Batini C, Weissenkampen JD, Liu M, Barnes DR, Bertelsen S, Chou YL, Erzurumluoglu AM, ... ... Foroud T, et al. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry. PMID 30679032 DOI: 10.1016/J.Biopsych.2018.11.024 |
0.373 |
|
| 2018 |
Marek K, Chowdhury S, Siderowf A, Lasch S, Coffey CS, Caspell-Garcia C, Simuni T, Jennings D, Tanner CM, Trojanowski JQ, Shaw LM, Seibyl J, Schuff N, Singleton A, Kieburtz K, ... ... Foroud T, et al. The Parkinson's progression markers initiative (PPMI) - establishing a PD biomarker cohort. Annals of Clinical and Translational Neurology. 5: 1460-1477. PMID 30564614 DOI: 10.1002/Acn3.644 |
0.37 |
|
| 2018 |
Budde M, Friedrichs S, Alliey-Rodriguez N, Ament S, Badner JA, Berrettini WH, Bloss CS, Byerley W, Cichon S, Comes AL, Coryell W, Craig DW, Degenhardt F, Edenberg HJ, Foroud T, et al. Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. PMID 30503783 DOI: 10.1016/J.Euroneuro.2018.10.005 |
0.38 |
|
| 2018 |
Breuer R, Mattheisen M, Frank J, Krumm B, Treutlein J, Kassem L, Strohmaier J, Herms S, Mühleisen TW, Degenhardt F, Cichon S, Nöthen MM, Karypis G, Kelsoe J, Greenwood T, ... ... Foroud T, et al. Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics. International Journal of Bipolar Disorders. 6: 24. PMID 30415424 DOI: 10.1186/S40345-018-0132-X |
0.343 |
|
| 2018 |
Chahine LM, Beach TG, Seedorff N, Caspell-Garcia C, Coffey CS, Brumm M, Adler CH, Serrano GE, Linder C, Mosovsky S, Foroud T, Riss H, Ecklund D, Seibyl J, Jennings D, et al. Feasibility and Safety of Multicenter Tissue and Biofluid Sampling for α-Synuclein in Parkinson's Disease: The Systemic Synuclein Sampling Study (S4). Journal of Parkinson's Disease. PMID 30248065 DOI: 10.3233/Jpd-181434 |
0.304 |
|
| 2018 |
Chen-Plotkin AS, Albin R, Alcalay R, Babcock D, Bajaj V, Bowman D, Buko A, Cedarbaum J, Chelsky D, Cookson MR, Dawson TM, Dewey R, Foroud T, Frasier M, German D, et al. Finding useful biomarkers for Parkinson's disease. Science Translational Medicine. 10. PMID 30111645 DOI: 10.1126/Scitranslmed.Aam6003 |
0.314 |
|
| 2018 |
Simuni T, Siderowf A, Lasch S, Coffey CS, Caspell-Garcia C, Jennings D, Tanner CM, Trojanowski JQ, Shaw LM, Seibyl J, Schuff N, Singleton A, Kieburtz K, Toga AW, Mollenhauer B, ... ... Foroud T, et al. Longitudinal change of clinical and biological measures in early Parkinson's disease: Parkinson's progression markers initiative cohort. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29572948 DOI: 10.1002/Mds.27361 |
0.315 |
|
| 2018 |
Verbrugge J, Rumbaugh M, Cook L, Schulze J, Miller M, Heathers L, Arnedo V, Kuhl MM, Foroud T. The Promise and Pitfalls of Facebook Advertising: a Genetic Counselor's Perspective. Journal of Genetic Counseling. PMID 29396840 DOI: 10.1007/S10897-017-0207-3 |
0.349 |
|
| 2018 |
Hui KY, Fernandez-Hernandez H, Hu J, Schaffner A, Pankratz N, Hsu NY, Chuang LS, Carmi S, Villaverde N, Li X, Rivas M, Levine AP, Bao X, Labrias PR, Haritunians T, ... ... Foroud T, et al. Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Science Translational Medicine. 10. PMID 29321258 DOI: 10.1126/Scitranslmed.Aai7795 |
0.59 |
|
| 2018 |
Touroutoglou A, Brickhouse M, Krivensky S, Wong B, Getchell K, Lucente D, McGinnis SM, Dickerson BC, Boeve BF, Rosen HJ, Boxer AL, Bove J, Brushaber D, Coppola G, Dheel C, ... ... Foroud T, et al. P1-419: Using A Brain Network Approach To Predict Genetic Mutation In Individual Patients With Familial Frontotemporal Dementia Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.428 |
0.312 |
|
| 2017 |
Agrawal A, Chou YL, Carey CE, Baranger DAA, Zhang B, Sherva R, Wetherill L, Kapoor M, Wang JC, Bertelsen S, Anokhin AP, Hesselbrock V, Kramer J, Lynskey MT, Meyers JL, ... ... Foroud T, et al. Genome-wide association study identifies a novel locus for cannabis dependence. Molecular Psychiatry. PMID 29112194 DOI: 10.1038/Mp.2017.200 |
0.359 |
|
| 2017 |
Wetherill L, Foroud T, Goodlett C. Meta-Analyses of Externalizing Disorders: Genetics or Prenatal Alcohol Exposure? Alcoholism, Clinical and Experimental Research. PMID 29063614 DOI: 10.1111/Acer.13535 |
0.301 |
|
| 2017 |
Horgusluoglu-Moloch E, Nho K, Risacher SL, Kim S, Foroud T, Shaw LM, Trojanowski JQ, Aisen PS, Petersen RC, Jack CR, Lovestone S, Simmons A, Weiner MW, Saykin AJ. Targeted neurogenesis pathway-based gene analysis identifies ADORA2A associated with hippocampal volume in mild cognitive impairment and Alzheimer's disease. Neurobiology of Aging. 60: 92-103. PMID 28941407 DOI: 10.1016/J.Neurobiolaging.2017.08.010 |
0.353 |
|
| 2017 |
Gwinn K, David KK, Swanson-Fischer C, Albin R, Hillaire-Clarke CS, Sieber BA, Lungu C, Bowman FD, Alcalay RN, Babcock D, Dawson TM, Dewey RB, Foroud T, German D, Huang X, et al. Parkinson's disease biomarkers: perspective from the NINDS Parkinson's Disease Biomarkers Program. Biomarkers in Medicine. PMID 28644039 DOI: 10.2217/Bmm-2016-0370 |
0.353 |
|
| 2017 |
Nho K, Kim S, Horgusluoglu E, Risacher SL, Shen L, Kim D, Lee S, Foroud T, Shaw LM, Trojanowski JQ, Aisen PS, Petersen RC, Jack CR, Weiner MW, Green RC, et al. Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer's disease. Bmc Medical Genomics. 10: 29. PMID 28589856 DOI: 10.1186/S12920-017-0267-0 |
0.372 |
|
| 2017 |
Landis BJ, Schubert JA, Lai D, Jegga AG, Shikany AR, Foroud T, Ware SM, Hinton RB. Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity. Journal of Cardiovascular Translational Research. PMID 28550590 DOI: 10.1007/S12265-017-9753-1 |
0.374 |
|
| 2017 |
DeMichele-Sweet MAA, Weamer EA, Klei L, Vrana DT, Hollingshead DJ, Seltman HJ, Sims R, Foroud T, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Ruiz A, Williams J, Mayeux R, et al. Genetic risk for schizophrenia and psychosis in Alzheimer disease. Molecular Psychiatry. PMID 28461698 DOI: 10.1038/Mp.2017.81 |
0.31 |
|
| 2017 |
Visanji NP, Mollenhauer B, Beach TG, Adler CH, Coffey CS, Kopil CM, Dave KD, Foroud T, Chahine L, Jennings D. The Systemic Synuclein Sampling Study: toward a biomarker for Parkinson's disease. Biomarkers in Medicine. PMID 28353371 DOI: 10.2217/Bmm-2016-0366 |
0.343 |
|
| 2017 |
Brockmann K, Schulte C, Schneiderhan-Marra N, Apel A, Pont-Sunyer C, Vilas D, Ruiz-Martinez J, Langkamp M, Corvol JC, Cormier F, Knorpp T, Joos TO, Bernard A, Gasser T, Marras C, ... ... Foroud T, et al. Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease. European Journal of Neurology. 24: 427-e6. PMID 28102045 DOI: 10.1111/Ene.13223 |
0.355 |
|
| 2017 |
Meyers JL, Zhang J, Wang JC, Su J, Kuo SI, Kapoor M, Wetherill L, Bertelsen S, Lai D, Salvatore JE, Kamarajan C, Chorlian D, Agrawal A, Almasy L, Bauer L, ... ... Foroud T, et al. An endophenotype approach to the genetics of alcohol dependence: a genome wide association study of fast beta EEG in families of African ancestry. Molecular Psychiatry. PMID 28070124 DOI: 10.1038/Mp.2016.239 |
0.399 |
|
| 2017 |
Ann A DeMichele-Sweet M, Weamer EA, Lambertus K, Vrana DT, Hollingshead DJ, Seltman HJ, Sims R, Foroud T, Hernandez I, Moreno-Grau S, Tarraga L, Boada M, Ruiz A, Williams J, Mayeux R, et al. [P3-102]: GENETIC RISK FOR SCHIZOPHRENIA AND PSYCHOSIS IN ALZHEIMER DISEASE Alzheimer's & Dementia. 13: P973-P974. DOI: 10.1016/J.Jalz.2017.06.1313 |
0.309 |
|
| 2016 |
Meyers JL, Zhang J, Manz N, Rangaswamy M, Kamarajan C, Wetherill L, Chorlian DB, Kang SJ, Bauer L, Hesselbrock V, Kramer J, Kuperman S, Nurnberger JI, Tischfield J, Wang JC, ... ... Foroud T, et al. A Genome Wide Association Study of Fast Beta EEG in Families of European Ancestry. International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology. PMID 28040410 DOI: 10.1016/J.Ijpsycho.2016.12.008 |
0.319 |
|
| 2016 |
Mez J, Chung J, Jun G, Kriegel J, Bourlas AP, Sherva R, Logue MW, Barnes LL, Bennett DA, Buxbaum JD, Byrd GS, Crane PK, Ertekin-Taner N, Evans D, Fallin MD, ... Foroud T, et al. Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 27770636 DOI: 10.1016/J.Jalz.2016.09.002 |
0.351 |
|
| 2016 |
Hopfner F, Haubenberger D, Galpern WR, Gwinn K, Van't Veer A, White S, Bhatia K, Adler CH, Eidelberg D, Ondo W, Stebbins GT, Tanner CM, Helmich RC, Lenz FA, Sillitoe RV, ... ... Foroud T, et al. Knowledge gaps and research recommendations for essential tremor. Parkinsonism & Related Disorders. PMID 27769649 DOI: 10.1016/J.Parkreldis.2016.10.002 |
0.34 |
|
| 2016 |
Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, ... ... Foroud T, et al. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology. PMID 27692902 DOI: 10.1016/S1474-4422(16)30203-4 |
0.373 |
|
| 2016 |
Nho K, Horgusluoglu E, Kim S, Risacher SL, Kim D, Foroud T, Aisen PS, Petersen RC, Jack CR, Shaw LM, Trojanowski JQ, Weiner MW, Green RC, Toga AW, Saykin AJ, et al. Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease. Bmc Medical Genomics. 9: 30. PMID 27535542 DOI: 10.1186/S12920-016-0190-9 |
0.353 |
|
| 2016 |
Hou L, Bergen SE, Akula N, Song J, Hultman CM, Landén M, Adli M, Alda M, Ardau R, Arias B, Aubry JM, Backlund L, Badner JA, Barrett TB, Bauer M, ... ... Foroud T, et al. Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Human Molecular Genetics. PMID 27329760 DOI: 10.1093/Hmg/Ddw181 |
0.386 |
|
| 2016 |
Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, ... ... Foroud T, et al. Identification of TMEM230 mutations in familial Parkinson's disease. Nature Genetics. PMID 27270108 DOI: 10.1038/Ng.3589 |
0.388 |
|
| 2016 |
Brockmann K, Apel A, Schulte C, Schneiderhan-Marra N, Pont-Sunyer C, Vilas D, Ruiz-Martinez J, Langkamp M, Corvol JC, Cormier F, Knorpp T, Joos TO, Gasser T, Schüle B, Aasly JO, ... Foroud T, et al. Inflammatory profile in LRRK2-associated prodromal and clinical PD. Journal of Neuroinflammation. 13: 122. PMID 27220776 DOI: 10.1186/S12974-016-0588-5 |
0.35 |
|
| 2016 |
Kapoor M, Chou YL, Edenberg HJ, Foroud T, Martin NG, Madden PA, Wang JC, Bertelsen S, Wetherill L, Brooks A, Chan G, Hesselbrock V, Kuperman S, Medland SE, Montgomery G, et al. Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures. Translational Psychiatry. 6: e761. PMID 27003187 DOI: 10.1038/Tp.2016.27 |
0.349 |
|
| 2016 |
Hui K, Fernandez-Hernandez H, Hu J, Pankratz N, Rivas M, Carmi S, Haritunians T, Atzmon G, Brant S, Daly M, Duerr R, McGovern D, Ostrer H, Rioux J, Silverberg M, ... Foroud T, et al. P-175 Pleiotropic Effects of Novel Functional LRRK2 Variation on Crohnʼs Disease and Parkinsonʼs Disease Risk Inflammatory Bowel Diseases. 22: S62-S63. DOI: 10.1097/01.Mib.0000480302.17090.47 |
0.569 |
|
| 2015 |
Farlow JL, Robak LA, Hetrick K, Bowling K, Boerwinkle E, Coban-Akdemir ZH, Gambin T, Gibbs RA, Gu S, Jain P, Jankovic J, Jhangiani S, Kaw K, Lai D, Lin H, ... ... Foroud T, et al. Whole-Exome Sequencing in Familial Parkinson Disease. Jama Neurology. 1-8. PMID 26595808 DOI: 10.1001/Jamaneurol.2015.3266 |
0.395 |
|
| 2015 |
Haas DM, Lai D, Sharma S, Then J, Kho A, Flockhart DA, Tantisira K, Foroud T. Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth. Reproductive Sciences (Thousand Oaks, Calif.). PMID 26507871 DOI: 10.1177/1933719115612129 |
0.312 |
|
| 2015 |
Foroud T, Smith D, Jackson J, Verbrugge J, Halter C, Wetherill L, Sims K, Xin W, Arnedo V, Lasch S, Marek K. Novel recruitment strategy to enrich for LRRK2 mutation carriers. Molecular Genetics & Genomic Medicine. 3: 404-12. PMID 26436106 DOI: 10.1002/Mgg3.151 |
0.345 |
|
| 2015 |
Barral S, Cheng R, Reitz C, Vardarajan B, Lee J, Kunkle B, Beecham G, Cantwell LS, Pericak-Vance MA, Farrer LA, Haines JL, Goate AM, Foroud T, Boerwinkle E, Schellenberg GD, et al. Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26433351 DOI: 10.1016/J.Jalz.2015.07.487 |
0.379 |
|
| 2015 |
Schwantes-An TH, Zhang J, Chen LS, Hartz SM, Culverhouse RC, Chen X, Coon H, Frank J, Kamens HM, Konte B, Kovanen L, Latvala A, Legrand LN, Maher BS, Melroy WE, ... ... Foroud T, et al. Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics. PMID 26392368 DOI: 10.1007/S10519-015-9737-3 |
0.339 |
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| 2015 |
Kunkle BW, Jaworski J, Barral S, Vardarajan B, Beecham GW, Martin ER, Cantwell LS, Partch A, Bird TD, Raskind WH, DeStefano AL, Carney RM, Cuccaro M, Vance JM, Farrer LA, ... ... Foroud T, et al. Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26365416 DOI: 10.1016/J.Jalz.2015.05.020 |
0.37 |
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| 2015 |
Alam I, Koller DL, Cañete T, Blázquez G, Mont-Cardona C, López-Aumatell R, Martínez-Membrives E, Díaz-Morán S, Tobeña A, Fernández-Teruel A, Stridh P, Diez M, Olsson T, Johannesson M, Baud A, ... ... Foroud T, et al. Fine mapping of bone structure and strength QTLs in heterogeneous stock rat. Bone. 81: 417-26. PMID 26297441 DOI: 10.1016/J.Bone.2015.08.013 |
0.348 |
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| 2015 |
Fullerton JM, Koller DL, Edenberg HJ, Foroud T, Liu H, Glowinski AL, McInnis MG, Wilcox HC, Frankland A, Roberts G, Schofield PR, Mitchell PB, Nurnberger JI. Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 168: 617-29. PMID 26178159 DOI: 10.1002/Ajmg.B.32344 |
0.362 |
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| 2015 |
Salvatore JE, Edwards AC, McClintick JN, Bigdeli TB, Adkins A, Aliev F, Edenberg HJ, Foroud T, Hesselbrock V, Kramer J, Nurnberger JI, Schuckit M, Tischfield JA, Xuei X, Dick DM. Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. Translational Psychiatry. 5: e558. PMID 25918995 DOI: 10.1038/Tp.2015.36 |
0.391 |
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| 2015 |
Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, ... ... Foroud T, et al. Variants associated with Gaucher disease in multiple system atrophy. Annals of Clinical and Translational Neurology. 2: 417-26. PMID 25909086 DOI: 10.1002/Acn3.185 |
0.392 |
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| 2015 |
Jin SC, Carrasquillo MM, Benitez BA, Skorupa T, Carrell D, Patel D, Lincoln S, Krishnan S, Kachadoorian M, Reitz C, Mayeux R, Wingo TS, Lah JJ, Levey AI, Murrell J, ... ... Foroud T, et al. TREM2 is associated with increased risk for Alzheimer's disease in African Americans. Molecular Neurodegeneration. 10: 19. PMID 25886450 DOI: 10.1186/S13024-015-0016-9 |
0.33 |
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| 2015 |
Whitfield JB, Rahman K, Haber PS, Day CP, Masson S, Daly AK, Cordell HJ, Mueller S, Seitz HK, Liangpunsakul S, Westerhold C, Liang T, Lumeng L, Foroud T, Nalpas B, et al. Brief report: genetics of alcoholic cirrhosis-GenomALC multinational study. Alcoholism, Clinical and Experimental Research. 39: 836-42. PMID 25872595 DOI: 10.1111/Acer.12693 |
0.319 |
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| 2015 |
Farlow JL, Lin H, Sauerbeck L, Lai D, Koller DL, Pugh E, Hetrick K, Ling H, Kleinloog R, van der Vlies P, Deelen P, Swertz MA, Verweij BH, Regli L, Rinkel GJ, ... ... Foroud T, et al. Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm. Plos One. 10: e0121104. PMID 25803036 DOI: 10.1371/Journal.Pone.0121104 |
0.382 |
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| 2015 |
Mackey J, Brown RD, Sauerbeck L, Hornung R, Moomaw CJ, Koller DL, Foroud T, Deka R, Woo D, Kleindorfer D, Flaherty ML, Meissner I, Anderson C, Rouleau G, Connolly ES, et al. Affected twins in the familial intracranial aneurysm study. Cerebrovascular Diseases (Basel, Switzerland). 39: 82-6. PMID 25571891 DOI: 10.1159/000369961 |
0.302 |
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| 2015 |
Wetherill L, Agrawal A, Kapoor M, Bertelsen S, Bierut LJ, Brooks A, Dick D, Hesselbrock M, Hesselbrock V, Koller DL, Le N, Nurnberger JI, Salvatore JE, Schuckit M, Tischfield JA, ... ... Foroud T, et al. Association of substance dependence phenotypes in the COGA sample. Addiction Biology. 20: 617-27. PMID 24832863 DOI: 10.1111/Adb.12153 |
0.404 |
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| 2015 |
Aliev F, Wetherill L, Bierut L, Bucholz KK, Edenberg H, Foroud T, Dick DM. Genes Associated With Alcohol Outcomes Show Enrichment of Effects With Broad Externalizing and Impulsivity Phenotypes in an Independent Sample Journal of Studies On Alcohol and Drugs. 76: 38-46. DOI: 10.15288/Jsad.2015.76.38 |
0.383 |
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| 2015 |
Horgusluoglu E, Nho K, Risacher SL, Foroud T, Saykin AJ. P1-002: Transcriptome-guided neurogenesis gene pathway variation is associated with hippocampal volume in mild cognitive impairment and Alzheimer's disease Alzheimer's & Dementia. 11: P336-P337. DOI: 10.1016/J.Jalz.2015.06.198 |
0.322 |
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| 2014 |
Ramanan VK, Nho K, Shen L, Risacher SL, Kim S, McDonald BC, Farlow MR, Foroud TM, Gao S, Soininen H, K?oszewska I, Mecocci P, Tsolaki M, Vellas B, Lovestone S, et al. FASTKD2 is associated with memory and hippocampal structure in older adults. Molecular Psychiatry. PMID 25385369 DOI: 10.1038/Mp.2014.142 |
0.317 |
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| 2014 |
Edenberg HJ, Foroud T. Genetics of alcoholism. Handbook of Clinical Neurology. 125: 561-71. PMID 25307596 DOI: 10.1016/B978-0-444-62619-6.00032-X |
0.388 |
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| 2014 |
Foroud T, Lai D, Koller D, Van't Hof F, Kurki MI, Anderson CS, Brown RD, Connolly ES, Eriksson JG, Flaherty M, Fornage M, von Und Zu Fraunberg M, Gaál EI, Laakso A, Hernesniemi J, et al. Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. Stroke; a Journal of Cerebral Circulation. 45: 3194-9. PMID 25256182 DOI: 10.1161/Strokeaha.114.006096 |
0.369 |
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| 2014 |
Perry JR, Day F, Elks CE, Sulem P, Thompson DJ, Ferreira T, He C, Chasman DI, Esko T, Thorleifsson G, Albrecht E, Ang WQ, Corre T, Cousminer DL, Feenstra B, ... ... Foroud T, et al. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature. 514: 92-7. PMID 25231870 DOI: 10.1038/Nature13545 |
0.362 |
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| 2014 |
Logue MW, Schu M, Vardarajan BN, Farrell J, Bennett DA, Buxbaum JD, Byrd GS, Ertekin-Taner N, Evans D, Foroud T, Goate A, Graff-Radford NR, Kamboh MI, Kukull WA, Manly JJ, et al. Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 609-618.e11. PMID 25172201 DOI: 10.1016/J.Jalz.2014.06.010 |
0.324 |
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| 2014 |
Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, ... ... Foroud T, et al. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics. 46: 989-93. PMID 25064009 DOI: 10.1038/Ng.3043 |
0.577 |
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| 2014 |
Jun G, Asai H, Zeldich E, Drapeau E, Chen C, Chung J, Park JH, Kim S, Haroutunian V, Foroud T, Kuwano R, Haines JL, Pericak-Vance MA, Schellenberg GD, Lunetta KL, et al. PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. Annals of Neurology. 76: 379-92. PMID 25043464 DOI: 10.1002/Ana.24219 |
0.348 |
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| 2014 |
Kapoor M, Wang JC, Wetherill L, Le N, Bertelsen S, Hinrichs AL, Budde J, Agrawal A, Almasy L, Bucholz K, Dick DM, Harari O, Xiaoling X, Hesselbrock V, Kramer J, ... ... Foroud T, et al. Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families. Drug and Alcohol Dependence. 142: 56-62. PMID 24962325 DOI: 10.1016/J.Drugalcdep.2014.05.023 |
0.371 |
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| 2014 |
Kemp JP, Medina-Gomez C, Estrada K, St Pourcain B, Heppe DH, Warrington NM, Oei L, Ring SM, Kruithof CJ, Timpson NJ, Wolber LE, Reppe S, Gautvik K, Grundberg E, Ge B, ... ... Foroud T, et al. Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment. Plos Genetics. 10: e1004423. PMID 24945404 DOI: 10.1371/Journal.Pgen.1004423 |
0.324 |
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| 2014 |
Alam I, Padgett LR, Ichikawa S, Alkhouli M, Koller DL, Lai D, Peacock M, Xuei X, Foroud T, Edenberg HJ, Econs MJ. SIBLING family genes and bone mineral density: Association and allele-specific expression in humans Bone. 64: 166-172. PMID 24747200 DOI: 10.1016/J.Bone.2014.04.013 |
0.347 |
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| 2014 |
Alam I, Koller DL, Cañete T, Blázquez G, López-Aumatell R, Martínez-Membrives E, Díaz-Morán S, Tobeña A, Fernández-Teruel A, Stridh P, Diez M, Olsson T, Johannesson M, Baud A, Econs MJ, ... Foroud T, et al. High-resolution genome screen for bone mineral density in heterogeneous stock rat. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 1619-26. PMID 24643965 DOI: 10.1002/Jbmr.2195 |
0.325 |
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| 2014 |
Hendrie HC, Murrell J, Baiyewu O, Lane KA, Purnell C, Ogunniyi A, Unverzagt FW, Hall K, Callahan CM, Saykin AJ, Gureje O, Hake A, Foroud T, Gao S. APOE ε4 and the risk for Alzheimer disease and cognitive decline in African Americans and Yoruba. International Psychogeriatrics / Ipa. 26: 977-85. PMID 24565289 DOI: 10.1017/S1041610214000167 |
0.304 |
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| 2014 |
Thompson PM, Stein JL, Medland SE, Hibar DP, Vasquez AA, Renteria ME, Toro R, Jahanshad N, Schumann G, Franke B, Wright MJ, Martin NG, Agartz I, Alda M, Alhusaini S, ... ... Foroud T, et al. The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior. 8: 153-82. PMID 24399358 DOI: 10.1007/S11682-013-9269-5 |
0.338 |
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| 2014 |
Agrawal A, Lynskey MT, Bucholz KK, Kapoor M, Almasy L, Dick DM, Edenberg HJ, Foroud T, Goate A, Hancock DB, Hartz S, Johnson EO, Hesselbrock V, Kramer JR, Kuperman S, et al. DSM-5 cannabis use disorder: a phenotypic and genomic perspective. Drug and Alcohol Dependence. 134: 362-9. PMID 24315570 DOI: 10.1016/J.Drugalcdep.2013.11.008 |
0.317 |
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| 2014 |
Wetherill L, Kapoor M, Agrawal A, Bucholz K, Koller D, Bertelsen SE, Le N, Wang JC, Almasy L, Hesselbrock V, Kramer J, Nurnberger JI, Schuckit M, Tischfield JA, Xuei X, ... ... Foroud T, et al. Family-based association analysis of alcohol dependence criteria and severity. Alcoholism, Clinical and Experimental Research. 38: 354-66. PMID 24015780 DOI: 10.1111/Acer.12251 |
0.356 |
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| 2014 |
Nho KT, Kim S, Risacher SL, Shen L, Foroud T, Aisen P, Petersen R, Jack C, Weiner MW, Green R, Toga A, Saykin AJ. P3-019: RARE VARIANT IN PLD3 IS ASSOCIATED WITH ALZHEIMER'S PATTERN OF NEURODEGENERATIVE CHANGES Alzheimer's & Dementia. 10: P634-P634. DOI: 10.1016/J.Jalz.2014.05.1106 |
0.302 |
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| 2014 |
Nho KT, Kim S, Risacher SL, Shen L, Foroud T, Aisen P, Petersen R, Jack C, Shaw L, Trojanowski JQ, Weiner MW, Green R, Toga A, Saykin AJ. P3-018: INFLUENCE OF RARE PSEN1 VARIANTS ON QUANTITATIVE STRUCTURAL IMAGING AND CSF PHENOTYPES IN LATE ONSET ALZHEIMER'S DISEASE Alzheimer's & Dementia. 10: P633-P633. DOI: 10.1016/J.Jalz.2014.05.1105 |
0.323 |
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| 2014 |
Nho KT, Kim S, Risacher SL, Shen L, Foroud T, Shaw L, Trojanowski JQ, Aisen P, Petersen R, Jack C, Weiner MW, Green R, Toga A, Saykin AJ. P3-017: ASSOCIATION ANALYSIS OF RARE VARIANTS NEAR THE APOE REGION WITH CEREBROSPINAL FLUID (CSF) BIOMARKERS OF ALZHEIMER'S DISEASE Alzheimer's & Dementia. 10: P632-P633. DOI: 10.1016/J.Jalz.2014.05.1104 |
0.317 |
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| 2013 |
Wang JC, Spiegel N, Bertelsen S, Le N, McKenna N, Budde JP, Harari O, Kapoor M, Brooks A, Hancock D, Tischfield J, Foroud T, Bierut LJ, Steinbach JH, Edenberg HJ, et al. Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry. Plos One. 8: e80204. PMID 24303001 DOI: 10.1371/Journal.Pone.0080204 |
0.331 |
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| 2013 |
Farlow JL, Foroud T. The genetics of dementia. Seminars in Neurology. 33: 417-22. PMID 24234360 DOI: 10.1055/S-0033-1359313 |
0.398 |
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| 2013 |
McClintick JN, Xuei X, Tischfield JA, Goate A, Foroud T, Wetherill L, Ehringer MA, Edenberg HJ. Stress-response pathways are altered in the hippocampus of chronic alcoholics. Alcohol (Fayetteville, N.Y.). 47: 505-15. PMID 23981442 DOI: 10.1016/J.Alcohol.2013.07.002 |
0.323 |
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| 2013 |
Chorlian DB, Rangaswamy M, Manz N, Wang JC, Dick D, Almasy L, Bauer L, Bucholz K, Foroud T, Hesselbrock V, Kang SJ, Kramer J, Kuperman S, Nurnberger J, Rice J, et al. Genetic and neurophysiological correlates of the age of onset of alcohol use disorders in adolescents and young adults. Behavior Genetics. 43: 386-401. PMID 23963516 DOI: 10.1007/S10519-013-9604-Z |
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| 2013 |
Mitsui J, Matsukawa T, Ishiura H, Fukuda Y, Ichikawa Y, Date H, Ahsan B, Nakahara Y, Momose Y, Takahashi Y, Iwata A, Goto J, Yamamoto Y, Komata M, Shirahige K, ... ... Foroud T, et al. Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration New England Journal of Medicine. 369: 233-244. PMID 23758206 DOI: 10.1056/Nejmoa1212115 |
0.4 |
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| 2013 |
Pichler I, Del Greco M F, Gögele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, Nalls M, Keller MF, Benyamin B, et al. Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study. Plos Medicine. 10: e1001462. PMID 23750121 DOI: 10.1371/Journal.Pmed.1001462 |
0.329 |
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| 2013 |
Kapoor M, Wang JC, Wetherill L, Le N, Bertelsen S, Hinrichs AL, Budde J, Agrawal A, Bucholz K, Dick D, Harari O, Hesselbrock V, Kramer J, Nurnberger JI, Rice J, ... ... Foroud T, et al. A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. Human Genetics. 132: 1141-51. PMID 23743675 DOI: 10.1007/S00439-013-1318-Z |
0.383 |
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| 2013 |
Edenberg HJ, Foroud T. Genetics and alcoholism. Nature Reviews. Gastroenterology & Hepatology. 10: 487-94. PMID 23712313 DOI: 10.1038/Nrgastro.2013.86 |
0.338 |
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| 2013 |
Foroud T. Whole exome sequencing of intracranial aneurysm. Stroke; a Journal of Cerebral Circulation. 44: S26-8. PMID 23709719 DOI: 10.1161/Strokeaha.113.001174 |
0.361 |
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| 2013 |
Baud A, Hermsen R, Guryev V, Stridh P, Graham D, McBride MW, Foroud T, Calderari S, Diez M, Ockinger J, Beyeen AD, Gillett A, Abdelmagid N, Guerreiro-Cacais AO, et al. Combined sequence-based and genetic mapping analysis of complex traits in outbred rats. Nature Genetics. 45: 767-75. PMID 23708188 DOI: 10.1038/Ng.2644 |
0.329 |
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| 2013 |
Reitz C, Tosto G, Vardarajan B, Rogaeva E, Ghani M, Rogers RS, Conrad C, Haines JL, Pericak-Vance MA, Fallin MD, Foroud T, Farrer LA, Schellenberg GD, George-Hyslop PS, Mayeux R, et al. Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational Psychiatry. 3: e256. PMID 23673467 DOI: 10.1038/Tp.2013.13 |
0.344 |
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| 2013 |
Nho K, Corneveaux JJ, Kim S, Lin H, Risacher SL, Shen L, Swaminathan S, Ramanan VK, Liu Y, Foroud T, Inlow MH, Siniard AL, Reiman RA, Aisen PS, Petersen RC, et al. Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment. Molecular Psychiatry. 18: 781-7. PMID 23608917 DOI: 10.1038/Mp.2013.24 |
0.36 |
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| 2013 |
Kos MZ, Yan J, Dick DM, Agrawal A, Bucholz KK, Rice JP, Johnson EO, Schuckit M, Kuperman S, Kramer J, Goate AM, Tischfield JA, Foroud T, Nurnberger J, Hesselbrock V, et al. Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. Genes, Brain, and Behavior. 12: 532-42. PMID 23607416 DOI: 10.1111/Gbb.12043 |
0.41 |
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| 2013 |
Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DM, Snowden J, ... ... Foroud T, et al. A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. Jama Neurology. 70: 727-35. PMID 23588557 DOI: 10.1001/Jamaneurol.2013.1925 |
0.601 |
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| 2013 |
Reitz C, Jun G, Naj A, Rajbhandary R, Vardarajan BN, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, Crane PK, Buxbaum JD, Murrell JR, ... ... Foroud TM, et al. Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. Jama. 309: 1483-92. PMID 23571587 DOI: 10.1001/Jama.2013.2973 |
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| 2013 |
Chen C, Cheng L, Grennan K, Pibiri F, Zhang C, Badner JA, Kelsoe JR, Greenwood TA, Nievergelt CM, Barrett TB, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, ... ... Foroud T, et al. Two gene co-expression modules differentiate psychotics and controls Molecular Psychiatry. 18: 1308-1314. PMID 23147385 DOI: 10.1038/Mp.2012.146 |
0.314 |
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| 2013 |
Wang JC, Foroud T, Hinrichs AL, Le NX, Bertelsen S, Budde JP, Harari O, Koller DL, Wetherill L, Agrawal A, Almasy L, Brooks AI, Bucholz K, Dick D, Hesselbrock V, et al. A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Molecular Psychiatry. 18: 1218-24. PMID 23089632 DOI: 10.1038/Mp.2012.143 |
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| 2013 |
Koller DL, Zheng HF, Karasik D, Yerges-Armstrong L, Liu CT, McGuigan F, Kemp JP, Giroux S, Lai D, Edenberg HJ, Peacock M, Czerwinski SA, Choh AC, McMahon G, St Pourcain B, ... ... Foroud T, et al. Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 28: 547-58. PMID 23074152 DOI: 10.1002/Jbmr.1796 |
0.336 |
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| 2013 |
Agrawal A, Wetherill L, Bucholz KK, Kramer J, Kuperman S, Lynskey MT, Nurnberger JI, Schuckit M, Tischfield JA, Edenberg HJ, Foroud T, Bierut LJ. Genetic influences on craving for alcohol Addictive Behaviors. 38: 1501-1508. PMID 22481050 DOI: 10.1016/J.Addbeh.2012.03.021 |
0.333 |
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| 2013 |
Vardarajan B, Bennett D, Bird T, Boeve B, Farlow M, Foroud T, Goate A, Graff-Radford N, Ottman R, Rosenberg RN, Schaid D, Sweet R, Tsuang D, Bennett J, Davis B, et al. Age-specific incidence rates of Alzheimer's disease in family members participating in the NIA-LOAD genetics study Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.1266 |
0.335 |
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| 2013 |
Jun G, Asai H, Drapeau E, Park J, Zeldich E, Chen C, Kim S, Foroud T, Lunetta K, Kim J, Buxbaum J, Abraham C, Ikezu T, Mayeux R, Farrer L. O4-06-02: Genetic variation in PLXNA4 associated with susceptibility of Alzheimer's disease through tau phosphorylation Alzheimer's & Dementia. 9: P692-P692. DOI: 10.1016/J.Jalz.2013.04.366 |
0.32 |
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| 2012 |
Swaminathan S, Huentelman MJ, Corneveaux JJ, Myers AJ, Faber KM, Foroud T, Mayeux R, Shen L, Kim S, Turk M, Hardy J, Reiman EM, Saykin AJ. Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Plos One. 7: e50640. PMID 23227193 DOI: 10.1371/Journal.Pone.0050640 |
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| 2012 |
Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini A, Corbani V, ... ... Foroud T, et al. Copy-number disorders are a common cause of congenital kidney malformations. American Journal of Human Genetics. 91: 987-97. PMID 23159250 DOI: 10.1016/J.Ajhg.2012.10.007 |
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| 2012 |
Nissen S, Liang S, Shehktman T, Kelsoe JR, Greenwood TA, Nievergelt CM, McKinney R, Shilling PD, Smith EN, Schork NJ, Bloss CS, Nurnberger JI, Edenberg HJ, Foroud T, et al. Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 941-50. PMID 23038240 DOI: 10.1002/Ajmg.B.32099 |
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| 2012 |
Meier S, Mattheisen M, Vassos E, Strohmaier J, Treutlein J, Josef F, Breuer R, Degenhardt F, Mühleisen TW, Müller-Myhsok B, Steffens M, Schmael C, McMahon FJ, Nöthen MM, ... ... Foroud T, et al. Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. Translational Psychiatry. 2: e165. PMID 23010768 DOI: 10.1038/Tp.2012.81 |
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| 2012 |
Foroud T, Koller DL, Lai D, Sauerbeck L, Anderson C, Ko N, Deka R, Mosley TH, Fornage M, Woo D, Moomaw CJ, Hornung R, Huston J, Meissner I, Bailey-Wilson JE, et al. Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk. Stroke; a Journal of Cerebral Circulation. 43: 2846-52. PMID 22961961 DOI: 10.1161/Strokeaha.112.656397 |
0.358 |
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| 2012 |
Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T, Beach TG, Myers RH. Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. Plos Genetics. 8: e1002794. PMID 22761592 DOI: 10.1371/Journal.Pgen.1002794 |
0.616 |
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| 2012 |
Teng M, Ichikawa S, Padgett LR, Wang Y, Mort M, Cooper DN, Koller DL, Foroud T, Edenberg HJ, Econs MJ, Liu Y. regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions. Bioinformatics (Oxford, England). 28: 1879-86. PMID 22611130 DOI: 10.1093/Bioinformatics/Bts275 |
0.36 |
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| 2012 |
Kang SJ, Rangaswamy M, Manz N, Wang JC, Wetherill L, Hinrichs T, Almasy L, Brooks A, Chorlian DB, Dick D, Hesselbrock V, Kramer J, Kuperman S, Nurnberger J, Rice J, ... ... Foroud T, et al. Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6. Genes, Brain, and Behavior. 11: 712-9. PMID 22554406 DOI: 10.1111/J.1601-183X.2012.00803.X |
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| 2012 |
Barral S, Bird T, Goate A, Farlow MR, Diaz-Arrastia R, Bennett DA, Graff-Radford N, Boeve BF, Sweet RA, Stern Y, Wilson RS, Foroud T, Ott J, Mayeux R. Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory. Neurology. 78: 1464-71. PMID 22539578 DOI: 10.1212/Wnl.0B013E3182553C48 |
0.366 |
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| 2012 |
Swaminathan S, Shen L, Kim S, Inlow M, West JD, Faber KM, Foroud T, Mayeux R, Saykin AJ. Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study. Current Alzheimer Research. 9: 801-14. PMID 22486522 DOI: 10.2174/156720512802455331 |
0.373 |
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| 2012 |
Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, ... ... Foroud T, et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Annals of Neurology. 71: 370-84. PMID 22451204 DOI: 10.1002/Ana.22687 |
0.613 |
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| 2012 |
Kapoor M, Wang JC, Bertelsen S, Bucholz K, Budde JP, Hinrichs A, Agrawal A, Brooks A, Chorlian D, Dick D, Hesselbrock V, Foroud T, Kramer J, Kuperman S, Manz N, et al. Variants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking. Plos One. 7: e33513. PMID 22438940 DOI: 10.1371/Journal.Pone.0033513 |
0.347 |
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| 2012 |
Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, ... ... Foroud T, et al. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Plos Genetics. 8: e1002548. PMID 22438815 DOI: 10.1371/Journal.Pgen.1002548 |
0.594 |
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| 2012 |
Bierut LJ, Goate AM, Breslau N, Johnson EO, Bertelsen S, Fox L, Agrawal A, Bucholz KK, Grucza R, Hesselbrock V, Kramer J, Kuperman S, Nurnberger J, Porjesz B, Saccone NL, ... ... Foroud T, et al. ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry. Molecular Psychiatry. 17: 445-50. PMID 21968928 DOI: 10.1038/Mp.2011.124 |
0.334 |
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| 2012 |
Wetherill L, Morzorati SL, Foroud T, Windisch K, Darlington T, Zimmerman US, Plawecki MH, O'Connor SJ. Subjective perceptions associated with the ascending and descending slopes of breath alcohol exposure vary with recent drinking history. Alcoholism, Clinical and Experimental Research. 36: 1050-7. PMID 21933199 DOI: 10.1111/J.1530-0277.2011.01642.X |
0.31 |
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| 2012 |
Swaminathan S, Shen L, Risacher SL, Yoder KK, West JD, Kim S, Nho K, Foroud T, Inlow M, Potkin SG, Huentelman MJ, Craig DW, Jagust WJ, Koeppe RA, Mathis CA, et al. Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. Brain Imaging and Behavior. 6: 1-15. PMID 21901424 DOI: 10.1007/S11682-011-9136-1 |
0.356 |
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| 2012 |
Rupp J, Dzemidzic M, Blekher T, West J, Hui S, Wojcieszek J, Saykin AJ, Kareken DA, Foroud T. Comparison of vertical and horizontal saccade measures and their relation to gray matter changes in premanifest and manifest Huntington disease. Journal of Neurology. 259: 267-76. PMID 21850389 DOI: 10.1007/S00415-011-6172-0 |
0.76 |
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| 2012 |
Badner JA, Koller D, Foroud T, Edenberg H, Nurnberger JI, Zandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, et al. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Molecular Psychiatry. 17: 818-26. PMID 21769101 DOI: 10.1038/Mp.2011.89 |
0.376 |
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| 2012 |
Reitz C, Manly J, Hall KS, Evans D, Bennett D, Buxbaum J, Ertekin-Taner N, Fallin D, Kamboh I, Foroud T, Goate A, Farrer L, Pericak-Vance M, Haines J, Mayeux R, et al. CTNNA3, CAPRIN2 and SPG20 are significantly associated with Alzheimer's disease in preliminary analyses of a genome-wide association study in African-Americans Alzheimers & Dementia. 8: 100. DOI: 10.1016/J.Jalz.2012.05.251 |
0.339 |
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| 2012 |
Ramanan V, Kim S, Holohan K, Shen L, Ngo K, Risacher S, Foroud T, Mukherjee S, Crane P, Aisen P, Petersen R, Weiner M, Saykin A. Common gene networks underlying memory impairment: A comparison of pathway analysis methods in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1844 |
0.306 |
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| 2012 |
Wang L, Valladares O, Lin C, Cantwell L, Foroud T, Schellenberg G. P4-116: The NIA Genetics of Alzheimer's Disease Data Storage Site (NIAGADS) Alzheimer's & Dementia. 8: P672-P672. DOI: 10.1016/J.Jalz.2012.05.1819 |
0.327 |
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| 2012 |
Swaminathan S, Huentelman M, Corneveaux J, Myers A, Faber K, Foroud T, Mayeux R, Shen L, Kim S, Turk M, Hardy J, Reiman E, Saykin A. Replication and meta-analysis of the CHRFAM7A copy number variant in a cohort of clinically characterized and neuropathologically verified individuals Alzheimers & Dementia. 8: 678. DOI: 10.1016/J.Jalz.2012.05.101 |
0.303 |
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| 2011 |
Schneider BP, Li L, Miller K, Flockhart D, Radovich M, Hancock BA, Kassem N, Foroud T, Koller DL, Badve SS, Li Z, Partridge AH, O'Neill AM, Sparano JA, Dang CT, et al. Genetic associations with taxane-induced neuropathy by a genome-wide association study (GWAS) in E5103. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 29: 1000. PMID 28020771 DOI: 10.1200/Jco.2011.29.15_Suppl.1000 |
0.312 |
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| 2011 |
Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, Edenberg HJ, Nurnberger JI, Rietschel M, Blackwood D, Corvin A, Flickinger M, Guan W, Mattingsdal M, McQuillin A, ... ... Foroud T, et al. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Nature Genetics. 43: 977-985. PMID 21926972 DOI: 10.1038/Ng.943 |
0.318 |
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| 2011 |
Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, ... ... Foroud T, et al. Translation initiator EIF4G1 mutations in familial Parkinson disease. American Journal of Human Genetics. 89: 398-406. PMID 21907011 DOI: 10.1016/J.Ajhg.2011.08.009 |
0.569 |
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| 2011 |
Pankratz N, Dumitriu A, Hetrick KN, Sun M, Latourelle JC, Wilk JB, Halter C, Doheny KF, Gusella JF, Nichols WC, Myers RH, Foroud T, DeStefano AL. Copy number variation in familial Parkinson disease. Plos One. 6: e20988. PMID 21829596 DOI: 10.1371/Journal.Pone.0020988 |
0.627 |
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| 2011 |
Smith EN, Koller DL, Panganiban C, Szelinger S, Zhang P, Badner JA, Barrett TB, Berrettini WH, Bloss CS, Byerley W, Coryell W, Edenberg HJ, Foroud T, Gershon ES, Greenwood TA, et al. Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. Plos Genetics. 7: e1002134. PMID 21738484 DOI: 10.1371/Journal.Pgen.1002134 |
0.395 |
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| 2011 |
Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T. Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 2039-44. PMID 21661047 DOI: 10.1002/Mds.23781 |
0.624 |
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| 2011 |
Swaminathan S, Kim S, Shen L, Risacher SL, Foroud T, Pankratz N, Potkin SG, Huentelman MJ, Craig DW, Weiner MW, Saykin AJ, The Alzheimer's Disease Neuroimaging Initiative Adni. Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. International Journal of Alzheimer's Disease. 2011: 729478. PMID 21660214 DOI: 10.4061/2011/729478 |
0.592 |
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| 2011 |
Reitz C, Rogaeva E, Foroud T, Farrer LA. Genetics and genomics of late-onset Alzheimer's disease and its endophenotypes. International Journal of Alzheimer's Disease. 2011: 284728. PMID 21660206 DOI: 10.4061/2011/284728 |
0.401 |
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| 2011 |
Hibar DP, Stein JL, Kohannim O, Jahanshad N, Saykin AJ, Shen L, Kim S, Pankratz N, Foroud T, Huentelman MJ, Potkin SG, Jack CR, Weiner MW, Toga AW, Thompson PM, et al. Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. Neuroimage. 56: 1875-91. PMID 21497199 DOI: 10.1016/J.Neuroimage.2011.03.077 |
0.603 |
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| 2011 |
Schumann G, Coin LJ, Lourdusamy A, Charoen P, Berger KH, Stacey D, Desrivières S, Aliev FA, Khan AA, Amin N, Aulchenko YS, Bakalkin G, Bakker SJ, Balkau B, Beulens JW, ... ... Foroud T, et al. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences of the United States of America. 108: 7119-24. PMID 21471458 DOI: 10.1073/Pnas.1017288108 |
0.372 |
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| 2011 |
Rupp J, Dzemidzic M, Blekher T, Bragulat V, West J, Jackson J, Hui S, Wojcieszek J, Saykin AJ, Kareken D, Foroud T. Abnormal error-related antisaccade activation in premanifest and early manifest Huntington disease. Neuropsychology. 25: 306-18. PMID 21401260 DOI: 10.1037/A0021873 |
0.771 |
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| 2011 |
Wijsman EM, Pankratz ND, Choi Y, Rothstein JH, Faber KM, Cheng R, Lee JH, Bird TD, Bennett DA, Diaz-Arrastia R, Goate AM, Farlow M, Ghetti B, Sweet RA, Foroud TM, et al. Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. Plos Genetics. 7: e1001308. PMID 21379329 DOI: 10.1371/Journal.Pgen.1001308 |
0.578 |
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| 2011 |
Zlojutro M, Manz N, Rangaswamy M, Xuei X, Flury-Wetherill L, Koller D, Bierut LJ, Goate A, Hesselbrock V, Kuperman S, Nurnberger J, Rice JP, Schuckit MA, Foroud T, Edenberg HJ, et al. Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 44-58. PMID 21184583 DOI: 10.1002/Ajmg.B.31136 |
0.428 |
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| 2011 |
Bice PJ, Lai D, Zhang L, Foroud T. Fine Mapping Quantitative Trait Loci that Influence Alcohol Preference Behavior in the High and Low Alcohol Preferring (HAP and LAP) Mice Behavior Genetics. 41: 565-570. PMID 21184168 DOI: 10.1007/S10519-010-9414-5 |
0.333 |
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| 2011 |
Kim S, Swaminathan S, Shen L, Risacher SL, Nho K, Foroud T, Shaw LM, Trojanowski JQ, Potkin SG, Huentelman MJ, Craig DW, DeChairo BM, Aisen PS, Petersen RC, Weiner MW, et al. Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort. Neurology. 76: 69-79. PMID 21123754 DOI: 10.1212/Wnl.0B013E318204A397 |
0.369 |
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| 2011 |
Schumann G, Coin LJ, Lourdusamy A, Charoen P, Berger KH, Stacey D, Desrivières S, Aliev FA, Khan AA, Amin N, Aulchenko YS, Bakalkin G, Bakker SJ, Balkau B, Beulens JW, ... ... Foroud T, et al. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124)) Proceedings of the National Academy of Sciences of the United States of America. 108: 9316. DOI: 10.1073/Pnas.1106917108 |
0.359 |
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| 2011 |
Kim S, Swaminathan S, Inlow M, Risacher S, Shen L, Foroud T, Shaw L, Trojanowski J, Soares H, Weiner M, Saykin A. Influence of genetic variation on plasma proteomics in AD, MCI and controls: Pairwise gene-protein analysis in the ADNI-1 cohort Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.09.084 |
0.302 |
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| 2011 |
Lee J, Cheng R, Pankratz N, Wijsman E, Bird T, Foroud T, Mayeux R. A Genome-Wide Study of Familial Alzheimer’s Disease Supports Additional Candidate Genes: The NIA-LOAD/NCRAD Family Study Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.524 |
0.582 |
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| 2010 |
Elks CE, Perry JR, Sulem P, Chasman DI, Franceschini N, He C, Lunetta KL, Visser JA, Byrne EM, Cousminer DL, Gudbjartsson DF, Esko T, Feenstra B, Hottenga JJ, Koller DL, ... ... Foroud T, et al. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics. 42: 1077-85. PMID 21102462 DOI: 10.1038/Ng.714 |
0.344 |
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| 2010 |
Derringer J, Krueger RF, Dick DM, Saccone S, Grucza RA, Agrawal A, Lin P, Almasy L, Edenberg HJ, Foroud T, Nurnberger JI, Hesselbrock VM, Kramer JR, Kuperman S, Porjesz B, et al. Predicting sensation seeking from dopamine genes. A candidate-system approach. Psychological Science. 21: 1282-90. PMID 20732903 DOI: 10.1177/0956797610380699 |
0.336 |
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| 2010 |
Bice PJ, Liang T, Zhang L, Graves TJ, Carr LG, Lai D, Kimpel MW, Foroud T. Fine mapping and expression of candidate genes within the chromosome 10 QTL region of the high and low alcohol-drinking rats. Alcohol (Fayetteville, N.Y.). 44: 477-85. PMID 20705418 DOI: 10.1016/J.Alcohol.2010.06.004 |
0.33 |
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| 2010 |
Kareken DA, Liang T, Wetherill L, Dzemidzic M, Bragulat V, Cox C, Talavage T, O'Connor SJ, Foroud T. A polymorphism in GABRA2 is associated with the medial frontal response to alcohol cues in an fMRI study. Alcoholism, Clinical and Experimental Research. 34: 2169-78. PMID 20698837 DOI: 10.1111/J.1530-0277.2010.01293.X |
0.333 |
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| 2010 |
Dick DM, Meyers J, Aliev F, Nurnberger J, Kramer J, Kuperman S, Porjesz B, Tischfield J, Edenberg HJ, Foroud T, Schuckit M, Goate A, Hesselbrock V, Bierut L. Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 1179-1188. PMID 20468071 DOI: 10.1002/Ajmg.B.31089 |
0.388 |
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| 2010 |
Ho AJ, Stein JL, Hua X, Lee S, Hibar DP, Leow AD, Dinov ID, Toga AW, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, et al. A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly. Proceedings of the National Academy of Sciences of the United States of America. 107: 8404-9. PMID 20404173 DOI: 10.1073/Pnas.0910878107 |
0.552 |
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| 2010 |
Chen AC, Manz N, Tang Y, Rangaswamy M, Almasy L, Kuperman S, Nurnberger J, O'Connor SJ, Edenberg HJ, Schuckit MA, Tischfield J, Foroud T, Bierut LJ, Rohrbaugh J, Rice JP, et al. Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence. Alcoholism, Clinical and Experimental Research. 34: 988-96. PMID 20374216 DOI: 10.1111/J.1530-0277.2010.01173.X |
0.389 |
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| 2010 |
Simon DK, Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Nichols WC, Foroud T. Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease. Bmc Medical Genetics. 11: 53. PMID 20356410 DOI: 10.1186/1471-2350-11-53 |
0.597 |
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| 2010 |
Bierut LJ, Agrawal A, Bucholz KK, Doheny KF, Laurie C, Pugh E, Fisher S, Fox L, Howells W, Bertelsen S, Hinrichs AL, Almasy L, Breslau N, Culverhouse RC, Dick DM, ... ... Foroud T, et al. A genome-wide association study of alcohol dependence. Proceedings of the National Academy of Sciences of the United States of America. 107: 5082-7. PMID 20202923 DOI: 10.1073/Pnas.0911109107 |
0.339 |
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| 2010 |
Edenberg HJ, Koller DL, Xuei X, Wetherill L, McClintick JN, Almasy L, Bierut LJ, Bucholz KK, Goate A, Aliev F, Dick D, Hesselbrock V, Hinrichs A, Kramer J, Kuperman S, ... ... Foroud T, et al. Genome-wide association study of alcohol dependence implicates a region on chromosome 11. Alcoholism, Clinical and Experimental Research. 34: 840-52. PMID 20201924 DOI: 10.1111/J.1530-0277.2010.01156.X |
0.403 |
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| 2010 |
Ichikawa S, Koller DL, Padgett LR, Lai D, Hui SL, Peacock M, Foroud T, Econs MJ. Replication of previous genome-wide association studies of bone mineral density in premenopausal American women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 1821-9. PMID 20200978 DOI: 10.1002/Jbmr.62 |
0.309 |
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| 2010 |
Stein JL, Hua X, Morra JH, Lee S, Hibar DP, Ho AJ, Leow AD, Toga AW, Sul JH, Kang HM, Eskin E, Saykin AJ, Shen L, Foroud T, Pankratz N, et al. Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Neuroimage. 51: 542-54. PMID 20197096 DOI: 10.1016/J.Neuroimage.2010.02.068 |
0.608 |
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| 2010 |
Deka R, Koller DL, Lai D, Indugula SR, Sun G, Woo D, Sauerbeck L, Moomaw CJ, Hornung R, Connolly ES, Anderson C, Rouleau G, Meissner I, Bailey-Wilson JE, Huston J, ... ... Foroud T, et al. The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm. Stroke; a Journal of Cerebral Circulation. 41: 1132-7. PMID 20190001 DOI: 10.1161/Strokeaha.109.574640 |
0.31 |
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| 2010 |
Wider C, Foroud T, Wszolek ZK. Clinical implications of gene discovery in Parkinson's disease and parkinsonism Movement Disorders. 25. PMID 20187245 DOI: 10.1002/Mds.22723 |
0.4 |
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| 2010 |
Stein JL, Hua X, Lee S, Ho AJ, Leow AD, Toga AW, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, Allen AN, Corneveaux JJ, et al. Voxelwise genome-wide association study (vGWAS). Neuroimage. 53: 1160-74. PMID 20171287 DOI: 10.1016/J.Neuroimage.2010.02.032 |
0.599 |
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| 2010 |
Shen L, Kim S, Risacher SL, Nho K, Swaminathan S, West JD, Foroud T, Pankratz N, Moore JH, Sloan CD, Huentelman MJ, Craig DW, Dechairo BM, Potkin SG, Jack CR, et al. Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. Neuroimage. 53: 1051-63. PMID 20100581 DOI: 10.1016/J.Neuroimage.2010.01.042 |
0.61 |
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| 2010 |
Rupp J, Blekher T, Jackson J, Beristain X, Marshall J, Hui S, Wojcieszek J, Foroud T. Progression in prediagnostic Huntington disease Journal of Neurology, Neurosurgery, and Psychiatry. 81: 379-384. PMID 19726414 DOI: 10.1136/Jnnp.2009.176982 |
0.769 |
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| 2010 |
Xuei X, Flury-Wetherill L, Dick D, Goate A, Tischfield J, Nurnberger J, Schuckit M, Kramer J, Kuperman S, Hesselbrock V, Porjesz B, Foroud T, Edenberg HJ. GABRR1 and GABRR2, encoding the GABA-A receptor subunits ρ1 and ρ2, are associated with alcohol dependence American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153: 418-427. PMID 19536785 DOI: 10.1002/Ajmg.B.30995 |
0.352 |
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| 2010 |
Swaminathan S, Kim S, Shen L, Risacher SL, Foroud T, Pankratz N, Potkin SG, Huentelman MJ, Craig DW, Weiner MW, Saykin AJ. Preliminary analysis of copy number variation in the ADNI cohort Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.050 |
0.541 |
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| 2009 |
Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T. Genomewide association study for onset age in Parkinson disease. Bmc Medical Genetics. 10: 98. PMID 19772629 DOI: 10.1186/1471-2350-10-98 |
0.638 |
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| 2009 |
Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Marder KS, Foroud T, Nichols WC. Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations. Neurology. 73: 279-86. PMID 19636047 DOI: 10.1212/Wnl.0B013E3181Af7A33 |
0.586 |
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| 2009 |
Spence JP, Liang T, Liu L, Johnson PL, Foroud T, Carr LG, Shekhar A. From QTL to candidate gene: a genetic approach to alcoholism research. Current Drug Abuse Reviews. 2: 127-34. PMID 19630743 DOI: 10.2174/1874473710902020127 |
0.362 |
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| 2009 |
Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W, Byerley W, Coryell W, Craig D, Edenberg HJ, Eskin E, Foroud T, Gershon E, Greenwood TA, Hipolito M, et al. Genome-wide association study of bipolar disorder in European American and African American individuals. Molecular Psychiatry. 14: 755-63. PMID 19488044 DOI: 10.1038/Mp.2009.43 |
0.356 |
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| 2009 |
Peacock M, Koller DL, Lai D, Hui S, Foroud T, Econs MJ. Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci. Bone. 45: 443-8. PMID 19427925 DOI: 10.1016/J.Bone.2009.05.002 |
0.311 |
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| 2009 |
Pankratz N, Nichols WC, Elsaesser VE, Pauciulo MW, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Pfeiffer RF, Foroud T. Alpha-synuclein and familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1125-31. PMID 19412953 DOI: 10.1002/Mds.22524 |
0.62 |
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| 2009 |
Nichols WC, Kissell DK, Pankratz N, Pauciulo MW, Elsaesser VE, Clark KA, Halter CA, Rudolph A, Wojcieszek J, Pfeiffer RF, Foroud T. Variation in GIGYF2 is not associated with Parkinson disease. Neurology. 72: 1886-92. PMID 19279319 DOI: 10.1212/01.Wnl.0000346517.98982.1B |
0.629 |
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| 2009 |
Blekher T, Weaver M, Rupp J, Nichols WC, Hui SL, Gray J, Yee RD, Wojcieszek J, Foroud T. Multiple step pattern as a biomarker in Parkinson disease Parkinsonism & Related Disorders. 15: 506-510. PMID 19211293 DOI: 10.1016/J.Parkreldis.2009.01.002 |
0.781 |
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| 2009 |
Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Epistasis between QTLs for bone density variation in Copenhagen x dark agouti F2 rats. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 20: 180-6. PMID 19153792 DOI: 10.1007/S00335-008-9161-6 |
0.337 |
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| 2009 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Langefeld C, Rouleau G, Connolly ES, Lai D, et al. Genome screen in familial intracranial aneurysm. Bmc Medical Genetics. 10: 3. PMID 19144135 DOI: 10.1186/1471-2350-10-3 |
0.312 |
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| 2009 |
Bice P, Valdar W, Zhang L, Liu L, Lai D, Grahame N, Flint J, Li TK, Lumeng L, Foroud T. Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice Alcoholism: Clinical and Experimental Research. 33: 531-537. PMID 19120064 DOI: 10.1111/J.1530-0277.2008.00866.X |
0.339 |
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| 2009 |
Zhang D, Cheng L, Qian Y, Alliey-Rodriguez N, Kelsoe JR, Greenwood T, Nievergelt C, Barrett TB, McKinney R, Schork N, Smith EN, Bloss C, Nurnberger J, Edenberg HJ, Foroud T, et al. Singleton deletions throughout the genome increase risk of bipolar disorder. Molecular Psychiatry. 14: 376-80. PMID 19114987 DOI: 10.1038/Mp.2008.144 |
0.33 |
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| 2009 |
Ichikawa S, Koller DL, Curry LR, Lai D, Xuei X, Edenberg HJ, Hui SL, Peacock M, Foroud T, Econs MJ. Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults. Calcified Tissue International. 84: 97-102. PMID 19093065 DOI: 10.1007/S00223-008-9200-Z |
0.302 |
|
| 2009 |
Agrawal A, Wetherill L, Dick DM, Xuei X, Hinrichs A, Hesselbrock V, Kramer J, Nurnberger JI, Schuckit M, Bierut LJ, Edenberg HJ, Foroud T. Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150: 736-740. PMID 19016476 DOI: 10.1002/Ajmg.B.30881 |
0.345 |
|
| 2009 |
Nichols WC, Pankratz N, Marek DK, Pauciulo MW, Elsaesser VE, Halter CA, Rudolph A, Wojcieszek J, Pfeiffer RF, Foroud T. Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset. Neurology. 72: 310-6. PMID 18987351 DOI: 10.1212/01.Wnl.0000327823.81237.D1 |
0.614 |
|
| 2009 |
Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Human Genetics. 124: 593-605. PMID 18985386 DOI: 10.1007/S00439-008-0582-9 |
0.627 |
|
| 2009 |
Worrall BB, Foroud T, Brown RD, Connolly ES, Hornung RW, Huston J, Kleindorfer D, Koller DL, Lai D, Moomaw CJ, Sauerbeck L, Woo D, Broderick JP. Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms. Stroke; a Journal of Cerebral Circulation. 40: 71-6. PMID 18948608 DOI: 10.1161/Strokeaha.108.522631 |
0.337 |
|
| 2009 |
Chen AC, Tang Y, Rangaswamy M, Wang JC, Almasy L, Foroud T, Edenberg HJ, Hesselbrock V, Nurnberger J, Kuperman S, O'Connor SJ, Schuckit MA, Bauer LO, Tischfield J, Rice JP, et al. Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 359-68. PMID 18618593 DOI: 10.1002/Ajmg.B.30818 |
0.392 |
|
| 2008 |
Liu L, Foroud T, Xuei X, Berrettini W, Byerley W, Coryell W, El-Mallakh R, Gershon ES, Kelsoe JR, Lawson WB, MacKinnon DF, McInnis M, McMahon FJ, Murphy DL, Rice J, et al. Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder. Psychiatric Genetics. 18: 267-74. PMID 19018231 DOI: 10.1097/Ypg.0B013E3283060F59 |
0.322 |
|
| 2008 |
Lee JH, Cheng R, Graff-Radford N, Foroud T, Mayeux R. Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci. Archives of Neurology. 65: 1518-26. PMID 19001172 DOI: 10.1001/Archneur.65.11.1518 |
0.401 |
|
| 2008 |
Wetherill L, Schuckit MA, Hesselbrock V, Xuei X, Liang T, Dick DM, Kramer J, Nurnberger JI, Tischfield JA, Porjesz B, Edenberg HJ, Foroud T. Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence. Alcoholism, Clinical and Experimental Research. 32: 2031-40. PMID 18828811 DOI: 10.1111/J.1530-0277.2008.00790.X |
0.327 |
|
| 2008 |
Pankratz N, Marder KS, Halter CA, Rudolph A, Shults CW, Nichols WC, Foroud T. Clinical correlates of depressive symptoms in familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 2216-23. PMID 18785635 DOI: 10.1002/Mds.22285 |
0.555 |
|
| 2008 |
Alam I, Sun Q, Liu L, Koller DL, Liu Y, Edenberg HJ, Econs MJ, Foroud T, Turner CH. Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck. Physiological Genomics. 35: 191-6. PMID 18728226 DOI: 10.1152/Physiolgenomics.90237.2008 |
0.316 |
|
| 2008 |
Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Linkage screen for BMD phenotypes in male and female COP and DA rat strains. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 1382-8. PMID 18707222 DOI: 10.1359/Jbmr.080401 |
0.316 |
|
| 2008 |
Ross J, Berrettini W, Coryell W, Gershon ES, Badner JA, Kelsoe JR, McInnis MG, McMahon FJ, Murphy DL, Nurnberger JI, Foroud T, Rice JP, Scheftner WB, Zandi P, Edenberg H, et al. Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20. Psychiatric Genetics. 18: 191-8. PMID 18628681 DOI: 10.1097/Ypg.0B013E3283050Aa5 |
0.36 |
|
| 2008 |
Bierut LJ, Stitzel JA, Wang JC, Hinrichs AL, Grucza RA, Xuei X, Saccone NL, Saccone SF, Bertelsen S, Fox L, Horton WJ, Breslau N, Budde J, Cloninger CR, Dick DM, ... Foroud T, et al. Variants in nicotinic receptors and risk for nicotine dependence. The American Journal of Psychiatry. 165: 1163-71. PMID 18519524 DOI: 10.1176/Appi.Ajp.2008.07111711 |
0.318 |
|
| 2008 |
Ichikawa S, Koller DL, Curry LR, Lai D, Xuei X, Pugh EW, Tsai YY, Doheny KF, Edenberg HJ, Hui SL, Foroud T, Peacock M, Econs MJ. Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 1680-8. PMID 18505370 DOI: 10.1359/Jbmr.080509 |
0.345 |
|
| 2008 |
Ghosh S, Bierut LJ, Porjesz B, Edenberg HJ, Dick D, Goate A, Hesselbrock V, Nurnberger J, Foroud T, Kramer J, Rice J, Begleiter H. A novel non-parametric regression reveals linkage on chromosome 4 for the number of externalizing symptoms in sib-pairs American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147: 1301-1305. PMID 18454434 DOI: 10.1002/Ajmg.B.30735 |
0.371 |
|
| 2008 |
Foroud T, Wetherill LF, Kramer J, Tischfield JA, Nurnberger JI, Schuckit MA, Xuei X, Edenberg HJ. The tachykinin receptor 3 is associated with alcohol and cocaine dependence. Alcoholism, Clinical and Experimental Research. 32: 1023-30. PMID 18422838 DOI: 10.1111/J.1530-0277.2008.00663.X |
0.346 |
|
| 2008 |
Haugarvoll K, Rademakers R, Kachergus JM, Nuytemans K, Ross OA, Gibson JM, Tan EK, Gaig C, Tolosa E, Goldwurm S, Guidi M, Riboldazzi G, Brown L, Walter U, Benecke R, ... ... Foroud T, et al. Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease. Neurology. 70: 1456-60. PMID 18337586 DOI: 10.1212/01.Wnl.0000304044.22253.03 |
0.364 |
|
| 2008 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Rouleau G, Connolly ES, Lai D, Koller DL, et al. Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study. Stroke; a Journal of Cerebral Circulation. 39: 1434-40. PMID 18323491 DOI: 10.1161/Strokeaha.107.502930 |
0.351 |
|
| 2008 |
Edenberg HJ, Wang J, Tian H, Pochareddy S, Xuei X, Wetherill L, Goate A, Hinrichs T, Kuperman S, Nurnberger JI, Schuckit M, Tischfield JA, Foroud T. A regulatory variation in OPRK1, the gene encoding the kappa-opioid receptor, is associated with alcohol dependence. Human Molecular Genetics. 17: 1783-9. PMID 18319328 DOI: 10.1093/Hmg/Ddn068 |
0.335 |
|
| 2008 |
Dick DM, Aliev F, Wang JC, Saccone S, Hinrichs A, Bertelsen S, Budde J, Saccone N, Foroud T, Nurnberger J, Xuei X, Conneally PM, Schuckit M, Almasy L, Crowe R, et al. A Systematic single nucleotide polymorphism screen to fine-map alcohol dependence genes on chromosome 7 identifies association with a novel susceptibility gene ACN9. Biological Psychiatry. 63: 1047-53. PMID 18163977 DOI: 10.1016/J.Biopsych.2007.11.005 |
0.407 |
|
| 2008 |
Edenberg HJ, Xuei X, Wetherill LF, Bierut L, Bucholz K, Dick DM, Hesselbrock V, Kuperman S, Porjesz B, Schuckit MA, Tischfield JA, Almasy LA, Nurnberger JI, Foroud T. Association of NFKB1, which encodes a subunit of the transcription factor NF-kappaB, with alcohol dependence. Human Molecular Genetics. 17: 963-70. PMID 18079108 DOI: 10.1093/Hmg/Ddm368 |
0.372 |
|
| 2008 |
Agrawal A, Hinrichs AL, Dunn G, Bertelsen S, Dick DM, Saccone SF, Saccone NL, Grucza RA, Wang JC, Cloninger CR, Edenberg HJ, Foroud T, Hesselbrock V, Kramer J, Bucholz KK, et al. Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample. Drug and Alcohol Dependence. 93: 12-20. PMID 17942244 DOI: 10.1016/J.Drugalcdep.2007.08.015 |
0.329 |
|
| 2008 |
Xuei X, Flury-Wetherill L, Almasy L, Bierut L, Tischfield J, Schuckit M, Nurnberger JI, Foroud T, Edenberg HJ. Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence. Addiction Biology. 13: 80-7. PMID 17910740 DOI: 10.1111/J.1369-1600.2007.00082.X |
0.338 |
|
| 2008 |
Foroud T, Ichikawa S, Koller D, Lai D, Curry L, Xuei X, Edenberg HJ, Hui S, Peacock M, Econs MJ. Association studies of ALOX5 and bone mineral density in healthy adults Osteoporosis International. 19: 637-643. PMID 17909879 DOI: 10.1007/S00198-007-0484-Z |
0.336 |
|
| 2008 |
Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Epistatic effects contribute to variation in BMD in Fischer 344 x Lewis F2 rats. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 41-7. PMID 17907919 DOI: 10.1359/Jbmr.071001 |
0.348 |
|
| 2008 |
Murrell J, Xuei X, Lane K, Flury L, Foroud T, Edenberg H, Unverzagt F, Hendrie H, Gao S, Hall K. P3-247: Apolipoprotein E polymorphisms associated with risk of Alzheimer's disease in elderly African-Americans Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1814 |
0.329 |
|
| 2007 |
Pankratz ND, Foroud T. Genetics of Parkinson disease. Genetics in Medicine. 9: 801-811. PMID 18091429 DOI: 10.1097/Gim.0B013E31815Bf97C |
0.612 |
|
| 2007 |
Stout JC, Weaver M, Solomon AC, Queller S, Hui S, Johnson SA, Gray J, Beristain X, Wojcieszek J, Foroud T. Are cognitive changes progressive in prediagnostic HD? Cognitive and Behavioral Neurology : Official Journal of the Society For Behavioral and Cognitive Neurology. 20: 212-8. PMID 18091069 DOI: 10.1097/Wnn.0B013E31815Cfef8 |
0.315 |
|
| 2007 |
Nichols WC, Elsaesser VE, Pankratz N, Pauciulo MW, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T. LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8 Neurology. 69: 1737-1744. PMID 17804834 DOI: 10.1212/01.Wnl.0000278115.50741.4E |
0.601 |
|
| 2007 |
Xuei X, Flury-Wetherill L, Bierut L, Dick D, Nurnberger J, Foroud T, Edenberg HJ. The opioid system in alcohol and drug dependence: Family-based association study American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144: 877-884. PMID 17503481 DOI: 10.1002/Ajmg.B.30531 |
0.323 |
|
| 2007 |
Foroud T, Wetherill LF, Liang T, Dick DM, Hesselbrock V, Kramer J, Nurnberger J, Schuckit M, Carr L, Porjesz B, Xuei X, Edenberg HJ. Association of alcohol craving with alpha-synuclein (SNCA). Alcoholism, Clinical and Experimental Research. 31: 537-45. PMID 17374032 DOI: 10.1111/J.1530-0277.2007.00337.X |
0.308 |
|
| 2007 |
Ioannidis JP, Ng MY, Sham PC, Zintzaras E, Lewis CM, Deng HW, Econs MJ, Karasik D, Devoto M, Kammerer CM, Spector T, Andrew T, Cupples LA, Duncan EL, Foroud T, et al. Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 22: 173-83. PMID 17228994 DOI: 10.1359/Jbmr.060806 |
0.306 |
|
| 2007 |
Nichols WC, Marek DK, Pauciulo MW, Pankratz N, Halter CA, Rudolph A, Shults CW, Wojcieszek J, Foroud T, Shults C, Marshall F, Oakes D, Shinaman A, Marder K, Conneally PM, et al. R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation Movement Disorders. 22: 254-257. PMID 17149721 DOI: 10.1002/Mds.21233 |
0.602 |
|
| 2006 |
Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T, Nichols WC, Shults C, Marshall F, Oakes D, Shinaman A, Marder K, Conneally PM, et al. Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease Movement Disorders. 21: 2257-2260. PMID 17078063 DOI: 10.1002/Mds.21162 |
0.581 |
|
| 2006 |
Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Shults CW, Foroud T, Nichols WC. Mutations in DJ-1 are rare in familial Parkinson disease Neuroscience Letters. 408: 209-213. PMID 16997464 DOI: 10.1016/J.Neulet.2006.09.003 |
0.615 |
|
| 2006 |
Edenberg HJ, Foroud T. The genetics of alcoholism: Identifying specific genes through family studies Addiction Biology. 11: 386-396. PMID 16961766 DOI: 10.1111/J.1369-1600.2006.00035.X |
0.418 |
|
| 2006 |
Johnson C, Drgon T, Liu QR, Walther D, Edenberg H, Rice J, Foroud T, Uhl GR. Pooled association genome scanning for alcohol dependence using 104,268 SNPs: validation and use to identify alcoholism vulnerability loci in unrelated individuals from the collaborative study on the genetics of alcoholism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 844-53. PMID 16894614 DOI: 10.1002/Ajmg.B.30346 |
0.373 |
|
| 2006 |
Jones KA, Porjesz B, Almasy L, Bierut L, Dick D, Goate A, Hinrichs A, Rice JP, Wang JC, Bauer LO, Crowe R, Foroud T, Hesselbrock V, Kuperman S, Nurnberger J, et al. A cholinergic receptor gene (CHRM2) affects event-related oscillations. Behavior Genetics. 36: 627-39. PMID 16823639 DOI: 10.1007/S10519-006-9075-6 |
0.31 |
|
| 2006 |
Dick DM, Plunkett J, Wetherill LF, Xuei X, Goate A, Hesselbrock V, Schuckit M, Crowe R, Edenberg HJ, Foroud T. Association between GABRA1 and drinking behaviors in the Collaborative Study on the Genetics of Alcoholism sample Alcoholism: Clinical and Experimental Research. 30: 1101-1110. PMID 16792556 DOI: 10.1111/J.1530-0277.2006.00136.X |
0.338 |
|
| 2006 |
Foroud T, Pankratz N, Martinez M. Chromosome 5 and Parkinson disease. European Journal of Human Genetics. 14: 1106-1110. PMID 16736031 DOI: 10.1038/Sj.Ejhg.5201666 |
0.622 |
|
| 2006 |
Agrawal A, Edenberg HJ, Foroud T, Bierut LJ, Dunne G, Hinrichs AL, Nurnberger JI, Crowe R, Kuperman S, Schuckit MA, Begleiter H, Porjesz B, Dick DM. Association of GABRA2 with drug dependence in the collaborative study of the genetics of alcoholism sample. Behavior Genetics. 36: 640-50. PMID 16622805 DOI: 10.1007/S10519-006-9069-4 |
0.346 |
|
| 2006 |
Edenberg HJ, Xuei X, Chen HJ, Tian H, Wetherill LF, Dick DM, Almasy L, Bierut L, Bucholz KK, Goate A, Hesselbrock V, Kuperman S, Nurnberger J, Porjesz B, Rice J, ... ... Foroud T, et al. Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis. Human Molecular Genetics. 15: 1539-49. PMID 16571603 DOI: 10.1093/Hmg/Ddl073 |
0.378 |
|
| 2006 |
Dick DM, Agrawal A, Schuckit MA, Bierut L, Hinrichs A, Fox L, Mullaney J, Cloninger CR, Hesselbrock V, Nurnberger JI, Almasy L, Foroud T, Porjesz B, Edenberg H, Begleiter H. Marital status, alcohol dependence, and GABRA2: evidence for gene-environment correlation and interaction. Journal of Studies On Alcohol. 67: 185-94. PMID 16562401 DOI: 10.15288/Jsa.2006.67.185 |
0.346 |
|
| 2006 |
Dick DM, Bierut L, Hinrichs A, Fox L, Bucholz KK, Kramer J, Kuperman S, Hesselbrock V, Schuckit M, Almasy L, Tischfield J, Porjesz B, Begleiter H, Nurnberger J, Xuei X, ... ... Foroud T, et al. The role of GABRA2 in risk for conduct disorder and alcohol and drug dependence across developmental stages. Behavior Genetics. 36: 577-90. PMID 16557364 DOI: 10.1007/S10519-005-9041-8 |
0.32 |
|
| 2006 |
Bice PJ, Foroud T, Carr LG, Zhang L, Liu L, Grahame NJ, Lumeng L, Li TK, Belknap JK. Identification of QTLs influencing alcohol preference in the High Alcohol Preferring (HAP) and Low Alcohol Preferring (LAP) mouse lines. Behavior Genetics. 36: 248-60. PMID 16482403 DOI: 10.1007/S10519-005-9019-6 |
0.334 |
|
| 2006 |
Carr LG, Habegger K, Spence JP, Liu L, Lumeng L, Foroud T. Development of congenic rat strains for alcohol consumption derived from the alcohol-preferring and nonpreferring rats. Behavior Genetics. 36: 285-90. PMID 16470346 DOI: 10.1007/S10519-005-9021-Z |
0.301 |
|
| 2006 |
Alam I, Sun Q, Liu L, Koller DL, Fishburn T, Carr LG, Econs MJ, Foroud T, Turner CH. Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength Bone. 39: 93-99. PMID 16461031 DOI: 10.1016/J.Bone.2005.12.009 |
0.318 |
|
| 2006 |
Hinrichs AL, Wang JC, Bufe B, Kwon JM, Budde J, Allen R, Bertelsen S, Evans W, Dick D, Rice J, Foroud T, Nurnberger J, Tischfield JA, Kuperman S, Crowe R, et al. Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence. American Journal of Human Genetics. 78: 103-11. PMID 16385453 DOI: 10.1086/499253 |
0.363 |
|
| 2006 |
Dick DM, Jones K, Saccone N, Hinrichs A, Wang JC, Goate A, Bierut L, Almasy L, Schuckit M, Hesselbrock V, Tischfield J, Foroud T, Edenberg H, Porjesz B, Begleiter H. Endophenotypes successfully lead to gene identification: results from the collaborative study on the genetics of alcoholism. Behavior Genetics. 36: 112-26. PMID 16341909 DOI: 10.1007/S10519-005-9001-3 |
0.376 |
|
| 2006 |
Pankratz N, Byder L, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC. Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 45-9. PMID 16116614 DOI: 10.1002/Mds.20663 |
0.634 |
|
| 2005 |
Pankratz N, Edenberg E, Foroud T. Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease Bmc Genetics. 6: 1-5. PMID 16451602 DOI: 10.1186/1471-2156-6-S1-S142 |
0.606 |
|
| 2005 |
Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC. A mutation in myotilin causes spheroid body myopathy. Neurology. 65: 1936-40. PMID 16380616 DOI: 10.1212/01.Wnl.0000188872.28149.9A |
0.55 |
|
| 2005 |
Gilman S, May SJ, Shults CW, Tanner CM, Kukull W, Lee VM, Masliah E, Low P, Sandroni P, Trojanowski JQ, Ozelius L, Foroud T. The North American Multiple System Atrophy Study Group. Journal of Neural Transmission (Vienna, Austria : 1996). 112: 1687-94. PMID 16284910 DOI: 10.1007/S00702-005-0381-6 |
0.303 |
|
| 2005 |
Duan QL, Nikpoor B, Dube MP, Molinaro G, Meijer IA, Dion P, Rochefort D, Saint-Onge J, Flury L, Brown NJ, Gainer JV, Rouleau JL, Agostoni A, Cugno M, Simon P, ... ... Foroud T, et al. A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors. American Journal of Human Genetics. 77: 617-26. PMID 16175507 DOI: 10.1086/496899 |
0.372 |
|
| 2005 |
McQueen MB, Devlin B, Faraone SV, Nimgaonkar VL, Sklar P, Smoller JW, Abou Jamra R, Albus M, Bacanu SA, Baron M, Barrett TB, Berrettini W, Blacker D, Byerley W, Cichon S, ... ... Foroud T, et al. Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q. American Journal of Human Genetics. 77: 582-95. PMID 16175504 DOI: 10.1086/491603 |
0.364 |
|
| 2005 |
Foroud T. LRRK2: both a cause and a risk factor for Parkinson disease? Neurology. 65: 664-665. PMID 16157895 DOI: 10.1212/01.Wnl.0000179342.58181.C9 |
0.383 |
|
| 2005 |
Chu K, Koller DL, Snyder R, Fishburn T, Lai D, Waguespack SG, Foroud T, Econs MJ. Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes. Bone. 37: 655-61. PMID 16120485 DOI: 10.1016/J.Bone.2005.06.003 |
0.419 |
|
| 2005 |
Broderick JP, Sauerbeck LR, Foroud T, Huston J, Pankratz N, Meissner I, Brown RD. The Familial Intracranial Aneurysm (FIA) study protocol Bmc Medical Genetics. 6: 17-17. PMID 15854227 DOI: 10.1186/1471-2350-6-17 |
0.535 |
|
| 2005 |
Spence J, Liang T, Foroud T, Lo D, Carr L. Expression profiling and QTL analysis: a powerful complementary strategy in drug abuse research. Addiction Biology. 10: 47-51. PMID 15849018 DOI: 10.1080/13556210412331308958 |
0.35 |
|
| 2005 |
Corbett J, Saccone NL, Foroud T, Goate A, Edenberg H, Nurnberger J, Porjesz B, Begleiter H, Reich T, Rice JP. A sex-adjusted and age-adjusted genome screen for nested alcohol dependence diagnoses. Psychiatric Genetics. 15: 25-30. PMID 15722954 DOI: 10.1097/00041444-200503000-00005 |
0.364 |
|
| 2005 |
Dick DM, Edenberg HJ, Xuei X, Goate A, Hesselbrock V, Schuckit M, Crowe R, Foroud T. No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample American Journal of Medical Genetics - Neuropsychiatric Genetics. 132: 24-28. PMID 15690551 DOI: 10.1002/Ajmg.B.30058 |
0.361 |
|
| 2005 |
Nichols WC, Pankratz N, Hernandez D, Paisán-Ruíz C, Jain S, Halter CA, Michaels VE, Reed T, Rudolph A, Shults CW, Singleton A, Foroud T. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet (London, England). 365: 410-2. PMID 15680455 DOI: 10.1016/S0140-6736(05)17828-3 |
0.607 |
|
| 2005 |
Koller DL, Ichikawa S, Johnson ML, Lai D, Xuei X, Edenberg HJ, Conneally PM, Hui SL, Johnston CC, Peacock M, Foroud T, Econs MJ. Contribution of the LRP5 gene to normal variation in peak BMD in women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 20: 75-80. PMID 15619672 DOI: 10.1359/Jbmr.041019 |
0.354 |
|
| 2004 |
Pankratz N, Foroud T. Genetics of Parkinson disease. Neurorx. 1: 235-242. PMID 15717024 DOI: 10.1602/Neurorx.1.2.235 |
0.638 |
|
| 2004 |
Liang T, Habegger K, Spence JP, Foroud T, Ellison JA, Lumeng L, Li TK, Carr LG. Glutathione S-transferase 8-8 expression is lower in alcohol-preferring than in alcohol-nonpreferring rats. Alcoholism, Clinical and Experimental Research. 28: 1622-8. PMID 15547447 DOI: 10.1097/01.Alc.0000145686.79141.57 |
0.309 |
|
| 2004 |
Koller DL, Peacock M, Lai D, Foroud T, Econs MJ. False positive rates in association studies as a function of degree of stratification. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 19: 1291-5. PMID 15231016 DOI: 10.1359/Jbmr.040409 |
0.346 |
|
| 2004 |
Jones KA, Porjesz B, Almasy L, Bierut L, Goate A, Wang JC, Dick DM, Hinrichs A, Kwon J, Rice JP, Rohrbaugh J, Stock H, Wu W, Bauer LO, Chorlian DB, ... ... Foroud T, et al. Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition. International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology. 53: 75-90. PMID 15210286 DOI: 10.1016/J.Ijpsycho.2004.02.004 |
0.304 |
|
| 2004 |
Nichols WC, Uniacke SK, Pankratz N, Reed T, Simon DK, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 649-55. PMID 15197702 DOI: 10.1002/Mds.20097 |
0.628 |
|
| 2004 |
Hesselbrock V, Dick D, Hesselbrock M, Foroud T, Schuckit M, Edenberg H, Bucholz K, Kramer J, Reich T, Goate A, Bierut L, Rice JP, Nurnberger JI. The search for genetic risk factors associated with suicidal behavior. Alcoholism, Clinical and Experimental Research. 28: 70S-76S. PMID 15166638 DOI: 10.1097/01.Alc.0000127416.92128.B0 |
0.305 |
|
| 2004 |
Pankratz N, Uniacke SK, Halter CA, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC. Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci. Neurology. 62: 1616-8. PMID 15136695 DOI: 10.1212/01.Wnl.0000123112.51368.10 |
0.635 |
|
| 2004 |
Reed T, Dick DM, Uniacke SK, Foroud T, Nichols WC. Genome-Wide Scan for a Healthy Aging Phenotype Provides Support for a Locus Near D4S1564 Promoting Healthy Aging Journals of Gerontology Series a-Biological Sciences and Medical Sciences. 59: 227-232. PMID 15031306 DOI: 10.1093/Gerona/59.3.B227 |
0.36 |
|
| 2004 |
Edenberg HJ, Dick DM, Xuei X, Tian H, Almasy L, Bauer LO, Crowe RR, Goate A, Hesselbrock V, Jones K, Kwon J, Li TK, Nurnberger JI, O'Connor SJ, Reich T, ... ... Foroud T, et al. Variations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations. American Journal of Human Genetics. 74: 705-14. PMID 15024690 DOI: 10.1086/383283 |
0.372 |
|
| 2004 |
Dick DM, Edenberg HJ, Xuei X, Goate A, Kuperman S, Schuckit M, Crowe R, Smith TL, Porjesz B, Begleiter H, Foroud T. Association of GABRG3 with alcohol dependence. Alcoholism, Clinical and Experimental Research. 28: 4-9. PMID 14745296 DOI: 10.1097/01.Alc.0000108645.54345.98 |
0.323 |
|
| 2004 |
Dick DM, Li TK, Edenberg HJ, Hesselbrock V, Kramer J, Kuperman S, Porjesz B, Bucholz K, Goate A, Nurnberger J, Foroud T. A genome-wide screen for genes influencing conduct disorder. Molecular Psychiatry. 9: 81-6. PMID 14699444 DOI: 10.1038/Sj.Mp.4001368 |
0.37 |
|
| 2004 |
Bierut LJ, Rice JP, Goate A, Hinrichs AL, Saccone NL, Foroud T, Edenberg HJ, Cloninger CR, Begleiter H, Conneally PM, Crowe RR, Hesselbrock V, Li TK, Nurnberger JI, Porjesz B, et al. A genomic scan for habitual smoking in families of alcoholics: common and specific genetic factors in substance dependence. American Journal of Medical Genetics. Part A. 124: 19-27. PMID 14679582 DOI: 10.1002/Ajmg.A.20329 |
0.341 |
|
| 2003 |
Pankratz N, Mukhopadhyay N, Huang S, Foroud T, Kirkwood SC. Identification of genes for complex disease using longitudinal phenotypes. Bmc Genetics. 4: S58. PMID 14975126 DOI: 10.1186/1471-2156-4-S1-S58 |
0.586 |
|
| 2003 |
Carr LG, Habegger K, Spence J, Ritchotte A, Liu L, Lumeng L, Li TK, Foroud T. Analyses of quantitative trait loci contributing to alcohol preference in HAD1/LAD1 and HAD2/LAD2 rats. Alcoholism, Clinical and Experimental Research. 27: 1710-7. PMID 14634485 DOI: 10.1097/01.Alc.0000097161.51093.71 |
0.313 |
|
| 2003 |
Liu Y, Xu F, Recker RR, Deng HW, Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Interpretation of Genetic Linkage Findings (multiple letters) Journal of Bone and Mineral Research. 18: 2077-2080. PMID 14606522 DOI: 10.1359/Jbmr.2003.18.11.2077 |
0.32 |
|
| 2003 |
Koller DL, Schriefer J, Sun Q, Shultz KL, Donahue LR, Rosen CJ, Foroud T, Beamer WG, Turner CH. Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1758-65. PMID 14584885 DOI: 10.1359/Jbmr.2003.18.10.1758 |
0.313 |
|
| 2003 |
Foroud T, Ritchotte A, Spence J, Liu L, Lumeng L, Li TK, Carr LG. Confirmation of alcohol preference quantitative trait loci in the replicate high alcohol drinking and low alcohol drinking rat lines. Psychiatric Genetics. 13: 155-61. PMID 12960747 DOI: 10.1097/00041444-200309000-00004 |
0.301 |
|
| 2003 |
Waguespack SG, Koller DL, White KE, Fishburn T, Carn G, Buckwalter KA, Johnson M, Kocisko M, Evans WE, Foroud T, Econs MJ. Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1513-8. PMID 12929941 DOI: 10.1359/Jbmr.2003.18.8.1513 |
0.363 |
|
| 2003 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Murrell J, Rudolph A, Shults CW, Conneally PM, Foroud T. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. Human Molecular Genetics. 12: 2599-608. PMID 12925570 DOI: 10.1093/Hmg/Ddg270 |
0.632 |
|
| 2003 |
Willour VL, Zandi PP, Huo Y, Diggs TL, Chellis JL, MacKinnon DF, Simpson SG, McMahon FJ, Potash JB, Gershon ES, Reich T, Foroud T, Nurnberger JI, DePaulo JR, McInnis MG. Genome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: chromosomes 4, 7, 9, 18, 19, 20, and 21. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 121: 21-7. PMID 12898570 DOI: 10.1002/Ajmg.B.20051 |
0.358 |
|
| 2003 |
Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1057-65. PMID 12817759 DOI: 10.1359/Jbmr.2003.18.6.1057 |
0.319 |
|
| 2003 |
Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, ... ... Foroud T, et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics. 73: 49-62. PMID 12802785 DOI: 10.1086/376547 |
0.337 |
|
| 2003 |
Dick DM, Foroud T, Flury L, Bowman ES, Miller MJ, Rau NL, Moe PR, Samavedy N, El-Mallakh R, Manji H, Glitz DA, Meyer ET, Smiley C, Hahn R, Widmark C, et al. Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. American Journal of Human Genetics. 73: 107-14. PMID 12772088 DOI: 10.1086/376562 |
0.326 |
|
| 2003 |
Dick DM, Foroud T. Candidate Genes for Alcohol Dependence: A Review of Genetic Evidence From Human Studies Alcoholism: Clinical and Experimental Research. 27: 868-879. PMID 12766633 DOI: 10.1097/01.Alc.0000065436.24221.63 |
0.336 |
|
| 2003 |
Zandi PP, Willour VL, Huo Y, Chellis J, Potash JB, MacKinnon DF, Simpson SG, McMahon FJ, Gershon E, Reich T, Foroud T, Nurnberger J, DePaulo JR, McInnis MG. Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 119: 69-76. PMID 12707942 DOI: 10.1002/Ajmg.B.10063 |
0.362 |
|
| 2003 |
Liang T, Spence J, Liu L, Strother WN, Chang HW, Ellison JA, Lumeng L, Li TK, Foroud T, Carr LG. alpha-Synuclein maps to a quantitative trait locus for alcohol preference and is differentially expressed in alcohol-preferring and -nonpreferring rats. Proceedings of the National Academy of Sciences of the United States of America. 100: 4690-5. PMID 12665621 DOI: 10.1073/Pnas.0737182100 |
0.303 |
|
| 2003 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Significant linkage of Parkinson disease to chromosome 2q36-37. American Journal of Human Genetics. 72: 1053-7. PMID 12638082 DOI: 10.1086/374383 |
0.612 |
|
| 2003 |
Foroud T, Uniacke SK, Liu L, Pankratz N, Rudolph A, Halter C, Shults C, Marder K, Conneally PM, Nichols WC. Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. Neurology. 60: 796-801. PMID 12629236 DOI: 10.1212/01.Wnl.0000049470.00180.07 |
0.612 |
|
| 2003 |
Ghosh S, Begleiter H, Porjesz B, Chorlian DB, Edenberg HJ, Foroud T, Goate A, Reich T. Linkage mapping of Beta 2 EEG waves via non-parametric regression American Journal of Medical Genetics - Neuropsychiatric Genetics. 118: 66-71. PMID 12627469 DOI: 10.1002/Ajmg.B.10057 |
0.335 |
|
| 2003 |
Reider CR, Halter CA, Castelluccio PF, Oakes D, Nichols WC, Foroud T. Reliability of reported age at onset for Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 275-9. PMID 12621630 DOI: 10.1002/Mds.10391 |
0.346 |
|
| 2003 |
Song J, Koller DL, Foroud T, Carr K, Zhao J, Rice J, Nurnberger JI, Begleiter H, Porjesz B, Smith TL, Schuckit MA, Edenberg HJ. Association of GABA(A) receptors and alcohol dependence and the effects of genetic imprinting. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 117: 39-45. PMID 12555233 DOI: 10.1002/Ajmg.B.10022 |
0.354 |
|
| 2002 |
Ramchandani VA, Flury L, Morzorati SL, Kareken D, Blekher T, Foroud T, Li TK, O'Connor S. Recent drinking history: association with family history of alcoholism and the acute response to alcohol during a 60 mg% clamp. Journal of Studies On Alcohol. 63: 734-44. PMID 12529074 DOI: 10.15288/Jsa.2002.63.734 |
0.312 |
|
| 2002 |
Dowsett SA, Archila L, Foroud T, Koller D, Eckert GJ, Kowolik MJ. The effect of shared genetic and environmental factors on periodontal disease parameters in untreated adult siblings in Guatemala. Journal of Periodontology. 73: 1160-8. PMID 12416774 DOI: 10.1902/Jop.2002.73.10.1160 |
0.351 |
|
| 2002 |
Dick DM, Nurnberger J, Edenberg HJ, Goate A, Crowe R, Rice J, Bucholz KK, Kramer J, Schuckit MA, Smith TL, Porjesz B, Begleiter H, Hesselbrock V, Foroud T. Suggestive linkage on chromosome 1 for a quantitative alcohol-related phenotype. Alcoholism, Clinical and Experimental Research. 26: 1453-60. PMID 12394277 DOI: 10.1111/J.1530-0277.2002.Tb02443.X |
0.378 |
|
| 2002 |
Close Kirkwood S, Siemers E, Viken RJ, Hodes ME, Conneally PM, Christian JC, Foroud T. Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales. Journal of Psychiatric Research. 36: 377-82. PMID 12393306 DOI: 10.1016/S0022-3956(02)00054-7 |
0.309 |
|
| 2002 |
Carr LG, Foroud T, Stewart T, Castelluccio P, Edenberg HJ, Li TK. Influence of ADH1B polymorphism on alcohol use and its subjective effects in a Jewish population American Journal of Medical Genetics. 112: 138-143. PMID 12244546 DOI: 10.1002/Ajmg.10674 |
0.31 |
|
| 2002 |
Carn G, Koller DL, Peacock M, Hui SL, Evans WE, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13. The Journal of Clinical Endocrinology and Metabolism. 87: 3819-24. PMID 12161516 DOI: 10.1210/Jcem.87.8.8740 |
0.368 |
|
| 2002 |
Nichols WC, Pankratz N, Uniacke SK, Pauciulo MW, Halter C, Rudolph A, Conneally PM, Foroud T. Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families. Journal of Medical Genetics. 39: 489-92. PMID 12114481 DOI: 10.1136/Jmg.39.7.489 |
0.625 |
|
| 2002 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. American Journal of Human Genetics. 71: 124-35. PMID 12058349 DOI: 10.1086/341282 |
0.633 |
|
| 2002 |
Peacock M, Turner CH, Econs MJ, Foroud T. Genetics of Osteoporosis Endocrine Reviews. 23: 303-326. PMID 12050122 DOI: 10.1210/Edrv.23.3.0464 |
0.321 |
|
| 2002 |
Dick DM, Foroud T, Edenberg HJ, Miller M, Bowman E, Rau NL, DePaulo JR, McInnis M, Gershon E, McMahon F, Rice JP, Bierut LJ, Reich T, Nurnberger J. Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees. American Journal of Medical Genetics. 114: 407-12. PMID 11992562 DOI: 10.1002/Ajmg.10380 |
0.366 |
|
| 2002 |
Foroud T, Bice P, Castelluccio P, Bo R, Ritchotte A, Stewart R, Lumeng L, Li TK, Carr L. Mapping of QTL influencing saccharin consumption in the selectively bred alcohol-preferring and -nonpreferring rat lines Behavior Genetics. 32: 57-67. PMID 11958543 DOI: 10.1023/A:1014459912935 |
0.335 |
|
| 2002 |
Saccone NL, Rice JP, Rochberg N, Williams JT, Goate A, Reich T, Edenberg HJ, Foroud T, Nurnberger JI, Bierut LJ, Crowe R, Li T. Linkage for Platelet Monoamine Oxidase (MAO) Activity: Results from a Replication Sample Alcoholism: Clinical and Experimental Research. 26: 603-609. DOI: 10.1111/J.1530-0277.2002.Tb02581.X |
0.329 |
|
| 2002 |
Blekher T, Ramchandani VA, Flury L, Foroud T, Kareken D, Yee RD, Li TK, O'Connor S. Saccadic eye movements are associated with a family history of alcoholism at baseline and after exposure to alcohol. Alcoholism: Clinical and Experimental Research. 26: 1568-1573. DOI: 10.1111/J.1530-0277.2002.Tb02457.X |
0.302 |
|
| 2001 |
Pankratz N, Kirkwood SC, Flury L, Koller DL, Foroud T. Use of variable marker density, principal components, and neural networks in the dissection of disease etiology Genetic Epidemiology. 21: S732-737. PMID 11793770 DOI: 10.1002/Gepi.2001.21.S1.S732 |
0.59 |
|
| 2001 |
McClintick J, Koller DL, Pankratz N, Kirkwood SC, Naughton B, Foroud T. Parametric linkage analysis and disequilibrium methods to identify loci for complex disease Genetic Epidemiology. 21: S528-S533. PMID 11793731 DOI: 10.1002/Gepi.2001.21.S1.S528 |
0.615 |
|
| 2001 |
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 413: 488-94. PMID 11586351 DOI: 10.1038/35097008 |
0.383 |
|
| 2001 |
Koller DL, Liu G, Econs MJ, Hui SL, Morin PA, Joslyn G, Rodriguez LA, Conneally PM, Christian JC, Johnston CC, Foroud T, Peacock M. Genome screen for quantitative trait loci underlying normal variation in femoral structure. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 16: 985-91. PMID 11393795 DOI: 10.1359/Jbmr.2001.16.6.985 |
0.329 |
|
| 2001 |
Nurnberger JI, Foroud T, Flury L, Su J, Meyer ET, Hu K, Crowe R, Edenberg H, Goate A, Bierut L, Reich T, Schuckit M, Reich W. Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder American Journal of Psychiatry. 158: 718-724. PMID 11329392 DOI: 10.1176/Appi.Ajp.158.5.718 |
0.305 |
|
| 2001 |
Schuckit MA, Edenberg HJ, Kalmijn J, Flury L, Smith TL, Reich T, Bierut L, Goate A, Foroud T. A genome-wide search for genes that relate to a low level of response to alcohol. Alcoholism, Clinical and Experimental Research. 25: 323-9. PMID 11290841 DOI: 10.1111/J.1530-0277.2001.Tb02217.X |
0.36 |
|
| 2001 |
Slager SL, Foroud T, Haghighi F, Spence MA, Hodge SE. Stoppage: an issue for segregation analysis. Genetic Epidemiology. 20: 328-339. PMID 11255242 DOI: 10.1002/Gepi.4 |
0.302 |
|
| 2001 |
Almasy L, Porjesz B, Blangero J, Goate A, Edenberg HJ, Chorlian DB, Kuperman S, O'Connor SJ, Rohrbaugh J, Bauer LO, Foroud T, Rice JP, Reich T, Begleiter H. Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism. American Journal of Human Genetics. 68: 128-135. PMID 11102287 DOI: 10.1086/316936 |
0.365 |
|
| 2000 |
Nurnberger JI, Foroud T. Genetics of bipolar affective disorder. Current Psychiatry Reports. 2: 147-157. PMID 11122948 DOI: 10.1007/S11920-000-0060-0 |
0.35 |
|
| 2000 |
Kirkwood SC, Siemers E, Hodes ME, Conneally PM, Christian JC, Foroud T. Subtle changes among presymptomatic carriers of the Huntington's disease gene. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 773-9. PMID 11080230 DOI: 10.1136/Jnnp.69.6.773 |
0.357 |
|
| 2000 |
Saccone NL, Kwon JM, Corbett J, Goate A, Rochberg N, Edenberg HJ, Foroud T, Li TK, Begleiter H, Reich T, Rice JP. A genome screen of maximum number of drinks as an alcoholism phenotype American Journal of Medical Genetics - Neuropsychiatric Genetics. 96: 632-637. PMID 11054770 DOI: 10.1002/1096-8628(20001009)96:5<632::Aid-Ajmg8>3.0.Co;2-# |
0.35 |
|
| 2000 |
Koller DL, Econs MJ, Morin PA, Christian JC, Hui SL, Parry P, Curran ME, Rodriguez LA, Conneally PM, Joslyn G, Peacock M, Johnston CC, Foroud T. Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. The Journal of Clinical Endocrinology and Metabolism. 85: 3116-20. PMID 10999795 DOI: 10.1210/Jcem.85.9.6778 |
0.334 |
|
| 2000 |
Foroud T, Bice P, Castelluccio P, Bo R, Miller L, Ritchotte A, Lumeng L, Li TK, Carr LG. Identification of quantitative trait loci influencing alcohol consumption in the high alcohol drinking and low alcohol drinking rat lines. Behavior Genetics. 30: 131-40. PMID 10979603 DOI: 10.1023/A:1001955205117 |
0.329 |
|
| 2000 |
Bierut LJ, Rice JP, Edenberg HJ, Goate A, Foroud T, Cloninger CR, Begleiter H, Conneally PM, Crowe RR, Hesselbrock V, Li TK, Nurnberger JI, Porjesz B, Schuckit MA, Reich T. Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking. American Journal of Medical Genetics. 90: 299-302. PMID 10710227 DOI: 10.1002/(Sici)1096-8628(20000214)90:4<299::Aid-Ajmg7>3.0.Co;2-Y |
0.313 |
|
| 2000 |
Foroud T, Castelluccio PF, Koller DL, Edenberg HJ, Miller M, Bowman E, Rau NL, Smiley C, Rice JP, Goate A, Armstrong C, Bierut LJ, Reich T, Detera-Wadleigh SD, Goldin LR, et al. Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees. American Journal of Medical Genetics. 96: 18-23. PMID 10686547 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<18::Aid-Ajmg6>3.0.Co;2-G |
0.341 |
|
| 2000 |
Pratt JH, Rebhun JF, Flury LL, Foroud T. Linkage of Nedd4, a Regulator of the Epithelial Sodium Channel, to Primary Hypertension in Blacks Hypertension. 36: 685-685. DOI: 10.1161/01.Hyp.36.Suppl_1.685 |
0.301 |
|
| 2000 |
Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li T, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, et al. Alcoholism Susceptibility Loci: Confirmation Studies in a Replicate Sample and Further Mapping Alcoholism: Clinical and Experimental Research. 24: 933-945. DOI: 10.1111/J.1530-0277.2000.Tb04634.X |
0.386 |
|
| 1999 |
Takacs I, Koller DL, Peacock M, Christian JC, Hui SL, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. The Journal of Clinical Endocrinology and Metabolism. 84: 4467-71. PMID 10599704 DOI: 10.1210/Jcem.84.12.6179 |
0.323 |
|
| 1999 |
Foroud T, Li T. Genetics of Alcoholism: A Review of Recent Studies in Human and Animal Models American Journal On Addictions. 8: 261-278. PMID 10598210 DOI: 10.1080/105504999305677 |
0.352 |
|
| 1999 |
Koller DL, Balding J, Foroud T. Nonparametric linkage and family-based association studies of a simulated complex disorder Genetic Epidemiology. 17: S627-S632. PMID 10597504 DOI: 10.1002/Gepi.13701707102 |
0.416 |
|
| 1999 |
Saccone NL, Rice JP, Rochberg N, Goate A, Reich T, Shears S, Wu W, Nurnberger JI, Foroud T, Edenberg HJ, Li TK. Genome screen for platelet monoamine oxidase (MAO) activity. American Journal of Medical Genetics. 88: 517-21. PMID 10490709 DOI: 10.1002/(Sici)1096-8628(19991015)88:5<517::Aid-Ajmg15>3.0.Co;2-B |
0.351 |
|
| 1999 |
Williams JT, Begleiter H, Porjesz B, Edenberg HJ, Foroud T, Reich T, Goate A, Van Eerdewegh P, Almasy L, Blangero J. Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. II. Alcoholism and event-related potentials. American Journal of Human Genetics. 65: 1148-60. PMID 10486334 DOI: 10.1086/302571 |
0.353 |
|
| 1999 |
Stoller ML, Bruce JE, Bruce CA, Foroud T, Kirkwood SC, Stambrook PJ. Linkage of type II and type III cystinuria to 19q13.1: Codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone- forming phenotype American Journal of Medical Genetics. 86: 134-139. PMID 10449648 DOI: 10.1002/(Sici)1096-8628(19990910)86:2<134::Aid-Ajmg9>3.0.Co;2-H |
0.333 |
|
| 1999 |
Detera-Wadleigh SD, Barden N, Craddock N, Ewald H, Foroud T, Kelsoe J, McQuillin A. Chromosomes 12 and 16 Workshop American Journal of Medical Genetics. 88: 255-259. PMID 10374740 DOI: 10.1002/(Sici)1096-8628(19990618)88:3<255::Aid-Ajmg8>3.0.Co;2-V |
0.404 |
|
| 1999 |
Craddock N, Lendon C, Cichon S, Culverhouse R, Detera-Wadleigh S, Devon R, Faraone S, Foroud T, Gejman P, Leonard S, McInnis M, Owen MJ, Riley B, Armstrong C, Barden N, et al. Chromosome Workshop: chromosomes 11, 14, and 15. American Journal of Medical Genetics. 88: 244-254. PMID 10374739 DOI: 10.1002/(Sici)1096-8628(19990618)88:3<244::Aid-Ajmg7>3.0.Co;2-1 |
0.313 |
|
| 1999 |
Wildenauer DB, Schwab SG, Blaveri A, Culverhouse R, Curtis D, Edwards J, Foroud T, Gershon E, Kelsoe J, Lichtermann D, McMahon F, Nurnberger J, Owen M, Todd R. Chromosomes 8 and 10 workshop. American Journal of Medical Genetics. 88: 239-243. PMID 10374738 DOI: 10.1002/(Sici)1096-8628(19990618)88:3<239::Aid-Ajmg6>3.0.Co;2-2 |
0.322 |
|
| 1999 |
Kirkwood SC, Siemers E, Stout JC, Hodes ME, Conneally PM, Christian JC, Foroud T. Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. Archives of Neurology. 56: 563-8. PMID 10328251 DOI: 10.1001/Archneur.56.5.563 |
0.345 |
|
| 1999 |
White KE, Koller DL, Takacs I, Buckwalter KA, Foroud T, Econs MJ. Locus heterogeneity of autosomal dominant osteopetrosis (ADO) Journal of Clinical Endocrinology and Metabolism. 84: 1047-1051. PMID 10084593 DOI: 10.1210/Jcem.84.3.5578 |
0.363 |
|
| 1999 |
Bice P, Foroud T, Bo R, Castelluccio P, Lumeng L, Li TK, Carr LG. Genomic screen for QTLs underlying alcohol consumption in the P and NP rat lines. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 949-55. PMID 9880658 DOI: 10.1007/S003359900905 |
0.338 |
|
| 1998 |
Koller DL, Rodriguez LA, Christian JC, Slemenda CW, Econs MJ, Hui SL, Morin P, Conneally PM, Joslyn G, Curran ME, Peacock M, Johnston CC, Foroud T. Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 13: 1903-8. PMID 9844108 DOI: 10.1359/Jbmr.1998.13.12.1903 |
0.344 |
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| 1998 |
Cloninger CR, Van Eerdewegh P, Goate A, Edenberg HJ, Blangero J, Hesselbrock V, Reich T, Nurnberger J, Schuckit M, Porjesz B, Crowe R, Rice JP, Foroud T, Przybeck TR, Almasy L, et al. Anxiety proneness linked to epistatic loci in genome scan of human personality traits. American Journal of Medical Genetics. 81: 313-7. PMID 9674977 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<313::Aid-Ajmg7>3.0.Co;2-U |
0.351 |
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| 1998 |
Begleiter H, Porjesz B, Reich T, Edenberg HJ, Goate A, Blangero J, Almasy L, Foroud T, Van Eerdewegh P, Polich J, Rohrbaugh J, Kuperman S, Bauer LO, O'Connor SJ, Chorlian DB, et al. Quantitative trait loci analysis of human event-related brain potentials: P3 voltage. Electroencephalography and Clinical Neurophysiology. 108: 244-50. PMID 9607513 DOI: 10.1016/S0168-5597(98)00002-1 |
0.343 |
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| 1998 |
Reich T, Edenberg HJ, Goate A, Williams JT, Rice JP, Van Eerdewegh P, Foroud T, Hesselbrock V, Schuckit MA, Bucholz K, Porjesz B, Li TK, Conneally PM, Nurnberger JI, Tischfield JA, et al. Genome-wide search for genes affecting the risk for alcohol dependence. American Journal of Medical Genetics. 81: 207-15. PMID 9603606 DOI: 10.1002/(Sici)1096-8628(19980508)81:3<207::Aid-Ajmg1>3.0.Co;2-T |
0.364 |
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| 1998 |
Dasouki MJ, Cogan J, Summar ML, Neblitt W, Foroud T, Koller D, Phillips JA. Heterogeneity in hereditary pancreatitis. American Journal of Medical Genetics. 77: 47-53. PMID 9557894 DOI: 10.1002/(Sici)1096-8628(19980428)77:1<47::Aid-Ajmg11>3.0.Co;2-O |
0.336 |
|
| 1998 |
Pratley RE, Thompson DB, Prochazka M, Baier L, Mott D, Ravussin E, Sakul H, Ehm MG, Burns DK, Foroud T, Garvey WT, Hanson RL, Knowler WC, Bennett PH, Bogardus C. An autosomal genomic scan for loci linked to prediabetic phenotypes in Pima Indians. The Journal of Clinical Investigation. 101: 1757-64. PMID 9541507 DOI: 10.1172/Jci1850 |
0.306 |
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| 1998 |
Porjesz B, Begleiter H, Reich T, Eerdewegh P, Edenberg HJ, Foroud T, Goate A, Litke A, Chorlian DB, Stirnus A, Rice J, Blangero J, Almasy L, Sorbell J, Bauer LO, et al. Amplitude of Visual P3 Event-Related Potential as a Phenotypic Marker for a Predisposition to Alcoholism: Preliminary Results from the COGA Project Alcoholism: Clinical and Experimental Research. 22: 1317-1323. DOI: 10.1111/J.1530-0277.1998.Tb03914.X |
0.343 |
|
| 1998 |
Carr LG, Foroud T, Bice P, Gobbett T, Ivashina J, Edenberg H, Lumeng L, Li T. A Quantitative Trait Locus for Alcohol Consumption in Selectively Bred Rat Lines Alcoholism: Clinical and Experimental Research. 22: 884-887. DOI: 10.1111/J.1530-0277.1998.Tb03883.X |
0.32 |
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| 1998 |
Edenberg HJ, Reynolds J, Koller DL, Begleiter H, Bucholz KK, Conneally PM, Crowe R, Goate A, Hesselbrock V, Li T, Numberger JI, Porjesz B, Reich T, Rice JP, Schuckit M, ... ... Foroud T, et al. A Family-Based Analysis of Whether the Functional Promoter Alleles of the Serotonin Transporter Gene HTT Affect the Risk for Alcohol Dependence Alcoholism: Clinical and Experimental Research. 22: 1080-1085. DOI: 10.1111/J.1530-0277.1998.Tb03704.X |
0.36 |
|
| 1998 |
Edenberg HJ, Foroud T, Koller DL, Goate A, Rice J, Eerdewegh P, Reich T, Cloninger CR, Nurnberger JI, Kowalczuk M, Wu B, Li T, Conneally PM, Tischfield JA, Wu W, et al. A Family-Based Analysis of the Association of the Dopamine D2 Receptor (DRD2) with Alcoholism Alcoholism: Clinical and Experimental Research. 22: 505-512. DOI: 10.1111/J.1530-0277.1998.Tb03680.X |
0.389 |
|
| 1998 |
Foroud T, Bucholz KK, Edenberg HJ, Goate A, Neuman RJ, Porjesz B, Koller DL, Ric J, Reich T, Bierut LJ, Cloninger CR, Nurnberger JI, Li T, Conneally PM, Tischfield JA, et al. Linkage of an Alcoholism-Related Severity Phenotype to Chromosome 16 Alcoholism: Clinical and Experimental Research. 22: 2035-2042. DOI: 10.1097/00000374-199812000-00020 |
0.367 |
|
| 1998 |
Kieburtz K, Frey K, Albin R, Marek K, Bates G, Aylward E, Guttman M, Rouleau G, Baehr M, Pahwa R, Lyons KE, Wilkinson SB, Kieltyka J, Koller WC, Bertoni JM, ... ... Foroud T, et al. Twelfth Annual Symposia on Etiology, Pathogenesis, and Treatment of Parkinson's Disease and Etiology, Pathogenesis, and Treatment of Huntington's Disease, Queen Elizabeth Hotel, Montreal, Canada, 18 October 1998 Movement Disorders. 13: 858-863. DOI: 10.1002/Mds.870130522 |
0.3 |
|
| 1997 |
Foroud T. Introduction to Genetic Linkage Analysis Cancer Investigation. 15: 548-552. PMID 9412660 DOI: 10.3109/07357909709047596 |
0.353 |
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| 1997 |
Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17. American Journal of Human Genetics. 61: 1131-8. PMID 9345089 DOI: 10.1086/301594 |
0.355 |
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| 1997 |
Stine OC, McMahon FJ, Chen L, Xu J, Meyers DA, MacKinnon DF, Simpson S, McInnis MG, Rice JP, Goate A, Reich T, Edenberg HJ, Foroud T, Nurnberger JI, Detera-Wadleigh SD, et al. Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X. American Journal of Medical Genetics. 74: 263-9. PMID 9184308 DOI: 10.1002/(Sici)1096-8628(19970531)74:3<263::Aid-Ajmg5>3.0.Co;2-R |
0.351 |
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| 1997 |
Rice JP, Goate A, Williams JT, Bierut L, Dorr D, Wu W, Shears S, Gopalakrishnan G, Edenberg HJ, Foroud T, Nurnberger J, Gershon ES, Detera-Wadleigh SD, Goldin LR, Guroff JJ, et al. Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12. American Journal of Medical Genetics. 74: 247-53. PMID 9184306 DOI: 10.1002/(Sici)1096-8628(19970531)74:3<247::Aid-Ajmg3>3.0.Co;2-N |
0.385 |
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| 1997 |
Edenberg HJ, Foroud T, Conneally PM, Sorbel JJ, Carr K, Crose C, Willig C, Zhao J, Miller M, Bowman E, Mayeda A, Rau NL, Smiley C, Rice JP, Goate A, et al. Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. American Journal of Medical Genetics. 74: 238-46. PMID 9184305 DOI: 10.1002/(Sici)1096-8628(19970531)74:3<238::Aid-Ajmg2>3.0.Co;2-M |
0.361 |
|
| 1997 |
Nurnberger JI, DePaulo JR, Gershon ES, Reich T, Blehar MC, Edenberg HJ, Foroud T, Miller M, Bowman E, Mayeda A, Rau NL, Smiley C, Conneally PM, McMahon F, Meyers D, et al. Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report American Journal of Medical Genetics - Neuropsychiatric Genetics. 74: 227-237. PMID 9184304 DOI: 10.1002/(Sici)1096-8628(19970531)74:3<227::Aid-Ajmg1>3.0.Co;2-N |
0.35 |
|
| 1997 |
Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32. Nature Genetics. 15: 277-80. PMID 9054941 DOI: 10.1038/Ng0397-277 |
0.324 |
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| 1996 |
Siemers E, Foroud T, Bill DJ, Sorbel J, Norton JA, Hodes ME, Niebler G, Conneally PM, Christian JC. Motor changes in presymptomatic Huntington disease gene carriers. Archives of Neurology. 53: 487-92. PMID 8660148 DOI: 10.1001/Archneur.1996.00550060029011 |
0.305 |
|
| 1995 |
Foroud T, Siemers E, Kleindorfer D, Bill DJ, Hodes ME, Norton JA, Conneally PM, Christian JC. Cognitive scores in carriers of Huntington's disease gene compared to noncarriers. Annals of Neurology. 37: 657-64. PMID 7755361 DOI: 10.1002/Ana.410370516 |
0.351 |
|
| 1992 |
Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. Nature Genetics. 1: 64-7. PMID 1363809 DOI: 10.1038/Ng0492-64 |
0.375 |
|
| 1992 |
Dlouhy SR, Farlow M, Hsiao K, Foroud T, Johnson P, Conneally PM, Prusiner SB, Hodes ME, Ghetti B. Linkage of the indiana kindred variant of Gerstmann-Sträussler-Scheinker disease to a mutation in the prion protein gene (PRNP)☆ Neurobiology of Aging. 13. DOI: 10.1016/0197-4580(92)90402-J |
0.344 |
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