| Year |
Citation |
Score |
| 2021 |
Halvorsen M, Samuels J, Wang Y, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Knowles JA, Zoghbi AW, Pottinger TD, Grados MA, Riddle MA, Bienvenu OJ, Nestadt PS, Krasnow J, ... ... Maher B, et al. Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variants. Nature Neuroscience. PMID 34183866 DOI: 10.1038/s41593-021-00876-8 |
0.308 |
|
| 2020 |
Johnson EC, Demontis D, Thorgeirsson TE, Walters RK, Polimanti R, Hatoum AS, Sanchez-Roige S, Paul SE, Wendt FR, Clarke TK, Lai D, Reginsson GW, Zhou H, He J, Baranger DAA, ... ... Maher BS, et al. A large-scale genome-wide association study meta-analysis of cannabis use disorder. The Lancet. Psychiatry. PMID 33096046 DOI: 10.1016/S2215-0366(20)30339-4 |
0.325 |
|
| 2020 |
Munn-Chernoff MA, Johnson EC, Chou YL, Coleman JRI, Thornton LM, Walters RK, Yilmaz Z, Baker JH, Hübel C, Gordon S, Medland SE, Watson HJ, Gaspar HA, Bryois J, Hinney A, ... ... Maher BS, et al. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. Addiction Biology. e12880. PMID 32064741 DOI: 10.1111/Adb.12880 |
0.418 |
|
| 2019 |
Samuels J, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, Mclaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, Mccracken JT, Piacentini J, et al. General personality dimensions, impairment and treatment response in obsessive-compulsive disorder. Personality and Mental Health. PMID 31859455 DOI: 10.1002/Pmh.1472 |
0.351 |
|
| 2019 |
Wang S, Maher B. Substance Use Disorder, Intravenous Injection, and HIV Infection: A Review. Cell Transplantation. 28: 1465-1471. PMID 31547679 DOI: 10.1177/0963689719878380 |
0.3 |
|
| 2019 |
Rabinowitz JA, Musci RJ, Reboussin B, Milam AJ, Benke KS, Uhl GR, Sisto DY, Ialongo NS, Maher BS. Polygenic and environmental influences on the course of African Americans' alcohol use from early adolescence through young adulthood. Development and Psychopathology. 1-16. PMID 31256767 DOI: 10.1017/S0954579419000701 |
0.307 |
|
| 2019 |
Bates TC, Maher BS, Colodro-Conde L, Medland SE, McAloney K, Wright MJ, Hansell NK, Okbay A, Kendler KS, Martin NG, Gillespie NA. Social Competence in Parents Increases Children's Educational Attainment: Replicable Genetically-Mediated Effects of Parenting Revealed by Non-Transmitted DNA. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-3. PMID 30661510 DOI: 10.1017/Thg.2018.75 |
0.31 |
|
| 2019 |
Rabinowitz JA, Musci R, Milam A, Benke K, Sisto D, Ialongo NS, Maher BS, Uhl G, Rosenbaum G, Reboussin B. Contributions of an internalizing symptoms polygenic risk score and contextual factors to alcohol-related disorders in african american young adults Journal of Studies On Alcohol and Drugs. 80: 77-85. DOI: 10.15288/Jsad.2019.80.77 |
0.319 |
|
| 2019 |
Halvorsen M, Goes F, Samuels JF, Wang Y, Maher B, Goldstein D, Nestadt G. 41 A Burden Of Rare Coding Variants In Obsessive Compulsive Disorder European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.07.182 |
0.312 |
|
| 2019 |
Bigdeli T, Bacanu S, Kelly B, Maher B, Knowles J, McCarroll S, Pato M, Pato C, Fanous A. WHOLE GENOME SEQUENCING OF MULTIPLY-AFFECTED SCHIZOPHRENIA AND BIPOLAR DISORDER FAMILIES FROM THE AZORES AND MADEIRA European Neuropsychopharmacology. 29: S1002-S1003. DOI: 10.1016/J.Euroneuro.2017.08.394 |
0.441 |
|
| 2018 |
Walters RK, Polimanti R, Johnson EC, McClintick JN, Adams MJ, Adkins AE, Aliev F, Bacanu SA, Batzler A, Bertelsen S, Biernacka JM, Bigdeli TB, Chen LS, Clarke TK, Chou YL, ... ... Maher BS, et al. Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience. 21: 1656-1669. PMID 30482948 DOI: 10.1038/S41593-018-0275-1 |
0.419 |
|
| 2018 |
Rabinowitz JA, Musci RJ, Milam AJ, Benke K, Uhl GR, Sisto DY, Ialongo NS, Maher BS. The interplay between externalizing disorders polygenic risk scores and contextual factors on the development of marijuana use disorders. Drug and Alcohol Dependence. 191: 365-373. PMID 30195949 DOI: 10.1016/J.Drugalcdep.2018.07.016 |
0.383 |
|
| 2018 |
Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... Maher B, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757 |
0.397 |
|
| 2018 |
Musci RJ, Bettencourt AF, Sisto D, Maher B, Uhl G, Ialongo N, Bradshaw CP. Evaluating the genetic susceptibility to peer reported bullying behaviors. Psychiatry Research. 263: 193-198. PMID 29573659 DOI: 10.1016/J.Psychres.2018.03.016 |
0.391 |
|
| 2018 |
Bates TC, Maher BS, Medland SE, McAloney K, Wright MJ, Hansell NK, Kendler KS, Martin NG, Gillespie NA. The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-11. PMID 29530109 DOI: 10.1017/Thg.2018.11 |
0.311 |
|
| 2018 |
Maher BS, Latendresse S, Vanyukov MM. Informing Prevention and Intervention Policy Using Genetic Studies of Resistance. Prevention Science. 19: 49-57. PMID 27943075 DOI: 10.1007/S11121-016-0730-8 |
0.332 |
|
| 2017 |
Samuels J, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, McLaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, McCracken JT, Piacentini J, et al. Self-reported executive function and hoarding in adults with obsessive-compulsive disorder. Comprehensive Psychiatry. 81: 53-59. PMID 29268152 DOI: 10.1016/J.Comppsych.2017.11.009 |
0.328 |
|
| 2017 |
Guo W, Samuels JF, Wang Y, Cao H, Ritter M, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, ... ... Maher B, et al. Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 27: 657-666. PMID 28641744 DOI: 10.1016/J.Euroneuro.2017.03.011 |
0.456 |
|
| 2017 |
Latendresse SJ, Musci R, Maher BS. Critical Issues in the Inclusion of Genetic and Epigenetic Information in Prevention and Intervention Trials. Prevention Science : the Official Journal of the Society For Prevention Research. PMID 28409280 DOI: 10.1007/S11121-017-0785-1 |
0.38 |
|
| 2017 |
Ritter ML, Guo W, Samuels JF, Wang Y, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, ... ... Maher B, et al. Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). Frontiers in Molecular Neuroscience. 10: 83. PMID 28386217 DOI: 10.3389/Fnmol.2017.00083 |
0.38 |
|
| 2017 |
Samuels J, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, McLaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, Nestadt P, McCracken JT, et al. An investigation of doubt in obsessive-compulsive disorder. Comprehensive Psychiatry. 75: 117-124. PMID 28359017 DOI: 10.1016/J.Comppsych.2017.03.004 |
0.318 |
|
| 2017 |
Lewis DD, Shaffer JR, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML. Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries. International Journal of Dentistry. 2017: 8465125. PMID 28348596 DOI: 10.1155/2017/8465125 |
0.311 |
|
| 2017 |
Adkins AE, Hack LM, Bigdeli TB, Williamson VS, McMichael GO, Mamdani M, Edwards A, Aliev F, Chan RF, Bhandari P, Raabe RC, Alaimo JT, Blackwell GG, Moscati AA, Poland RS, ... ... Maher BS, et al. Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-response Behaviors in Model Organisms. Alcoholism, Clinical and Experimental Research. PMID 28226201 DOI: 10.1111/Acer.13362 |
0.313 |
|
| 2017 |
Eckert S, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML, Shaffer JR. Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries. Journal of Human Genetics. PMID 28100911 DOI: 10.1038/Jhg.2016.161 |
0.39 |
|
| 2016 |
Chen D, Bienvenu OJ, Krasnow J, Wang Y, Grados MA, Cullen B, Goes FS, Maher B, Greenberg BD, McLaughlin NC, Rasmussen SA, Fyer AJ, Knowles JA, McCracken JT, Piacentini J, et al. Parental bonding and hoarding in obsessive-compulsive disorder. Comprehensive Psychiatry. 73: 43-52. PMID 27915218 DOI: 10.1016/J.Comppsych.2016.11.004 |
0.31 |
|
| 2016 |
Musci RJ, Fairman B, Masyn KE, Uhl G, Maher B, Sisto DY, Kellam SG, Ialongo NS. Polygenic Score × Intervention Moderation: an Application of Discrete-Time Survival Analysis to Model the Timing of First Marijuana Use Among Urban Youth. Prevention Science : the Official Journal of the Society For Prevention Research. PMID 27817095 DOI: 10.1007/S11121-016-0729-1 |
0.312 |
|
| 2016 |
Park JM, Samuels JF, Grados MA, Riddle MA, Bienvenu OJ, Goes FS, Cullen B, Wang Y, Krasnow J, Murphy DL, Rasmussen SA, McLaughlin NC, Piacentini J, Pauls DL, Stewart SE, ... ... Maher B, et al. ADHD and executive functioning deficits in OCD youths who hoard. Journal of Psychiatric Research. 82: 141-148. PMID 27501140 DOI: 10.1016/J.Jpsychires.2016.07.024 |
0.327 |
|
| 2016 |
Otowa T, Hek K, Lee M, Byrne EM, Mirza SS, Nivard MG, Bigdeli T, Aggen SH, Adkins D, Wolen A, Fanous A, Keller MC, Castelao E, Kutalik Z, der Auwera SV, ... ... Maher BS, et al. Meta-analysis of genome-wide association studies of anxiety disorders. Molecular Psychiatry. PMID 26857599 DOI: 10.1038/mp.2016.11 |
0.449 |
|
| 2016 |
Otowa T, Hek K, Lee M, Byrne EM, Mirza SS, Nivard MG, Bigdeli T, Aggen SH, Adkins D, Wolen A, Fanous A, Keller MC, Castelao E, Kutalik Z, der Auwera SV, ... ... Maher BS, et al. Meta-analysis of genome-wide association studies of anxiety disorders. Molecular Psychiatry. PMID 26754954 DOI: 10.1038/Mp.2015.197 |
0.437 |
|
| 2016 |
Vanyukov M, Cornelius M, Genna ND, Reynolds M, Kirillova G, Maher B, Kirisci L. Measurement of Liability to Addiction: Dimensional Approaches The International Journal of Person-Centered Medicine. 6. DOI: 10.5750/Ijpcm.V6I4.612 |
0.337 |
|
| 2015 |
Maher BS. Polygenic Scores in Epidemiology: Risk Prediction, Etiology, and Clinical Utility. Current Epidemiology Reports. 2: 239-244. PMID 26664818 DOI: 10.1007/S40471-015-0055-3 |
0.353 |
|
| 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, 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 |
0.375 |
|
| 2015 |
Edwards AC, Bigdeli TB, Docherty AR, Bacanu S, Lee D, de Candia TR, Moscati A, Thiselton DL, Maher BS, Wormley BK, Walsh D, O'Neill FA, Kendler KS, Riley BP, Fanous AH. Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes. Schizophrenia Bulletin. PMID 26316594 DOI: 10.1093/Schbul/Sbv119 |
0.373 |
|
| 2015 |
Musci RJ, Masyn KE, Benke K, Maher B, Uhl G, Ialongo NS. The effects of the interplay of genetics and early environmental risk on the course of internalizing symptoms from late childhood through adolescence. Development and Psychopathology. 1-13. PMID 25936925 DOI: 10.1017/S0954579415000401 |
0.371 |
|
| 2015 |
Shaffer JR, Carlson JC, Stanley BO, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, et al. Effects of enamel matrix genes on dental caries are moderated by fluoride exposures. Human Genetics. 134: 159-67. PMID 25373699 DOI: 10.1007/S00439-014-1504-7 |
0.393 |
|
| 2014 |
Otowa T, Maher BS, Aggen SH, McClay JL, van den Oord EJ, Hettema JM. Genome-wide and gene-based association studies of anxiety disorders in European and African American samples. Plos One. 9: e112559. PMID 25390645 DOI: 10.1371/Journal.Pone.0112559 |
0.419 |
|
| 2014 |
Samuels J, Grados MA, Riddle MA, Bienvenu OJ, Goes FS, Cullen B, Wang Y, Greenberg BD, Fyer AJ, McCracken JT, Geller D, Murphy DL, Knowles JA, Rasmussen SA, McLaughlin NC, ... ... Maher B, et al. Hoarding in Children and Adolescents with Obsessive-Compulsive Disorder. Journal of Obsessive-Compulsive and Related Disorders. 3: 325-331. PMID 25309849 DOI: 10.1016/J.Jocrd.2014.08.001 |
0.329 |
|
| 2014 |
Guintivano J, Brown T, Newcomer A, Jones M, Cox O, Maher BS, Eaton WW, Payne JL, Wilcox HC, Kaminsky ZA. Identification and replication of a combined epigenetic and genetic biomarker predicting suicide and suicidal behaviors. The American Journal of Psychiatry. 171: 1287-96. PMID 25073599 DOI: 10.1016/J.Comppsych.2014.08.024 |
0.312 |
|
| 2014 |
Stanley BO, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML, Shaffer JR. Genetic Association of MPPED2 and ACTN2 with Dental Caries. Journal of Dental Research. 93: 626-632. PMID 24810274 DOI: 10.1177/0022034514534688 |
0.396 |
|
| 2014 |
Samuels J, Shugart YY, Wang Y, Grados MA, Bienvenu OJ, Pinto A, Rauch SL, Greenberg BD, Knowles JA, Fyer AJ, Piacentini J, Pauls DL, Cullen B, Rasmussen SA, Stewart SE, ... ... Maher BS, et al. Clinical correlates and genetic linkage of social and communication difficulties in families with obsessive-compulsive disorder: Results from the OCD Collaborative Genetics Study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 326-36. PMID 24798771 DOI: 10.1002/Ajmg.B.32235 |
0.373 |
|
| 2014 |
Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, et al. An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Human Molecular Genetics. 23: 3316-26. PMID 24474471 DOI: 10.1093/Hmg/Ddu025 |
0.4 |
|
| 2014 |
Musci RJ, Bradshaw CP, Maher B, Uhl GR, Kellam SG, Ialongo NS. Reducing aggression and impulsivity through school-based prevention programs: a gene by intervention interaction. Prevention Science : the Official Journal of the Society For Prevention Research. 15: 831-40. PMID 24178584 DOI: 10.1007/S11121-013-0441-3 |
0.322 |
|
| 2013 |
Weinberg SM, Parsons TE, Marazita ML, Maher BS. Heritability of Face Shape in Twins: A Preliminary Study using 3D Stereophotogrammetry and Geometric Morphometrics. Dentistry 3000. 1. PMID 24501696 DOI: 10.5195/D3000.2013.14 |
0.304 |
|
| 2013 |
Bigdeli TB, Maher BS, Zhao Z, Sun J, Medeiros H, Akula N, McMahon FJ, Carvalho C, Ferreira SR, Azevedo MH, Knowles JA, Pato MT, Pato CN, Fanous AH. Association study of 83 candidate genes for bipolar disorder in chromosome 6q selected using an evidence-based prioritization algorithm. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 898-906. PMID 24123842 DOI: 10.1002/Ajmg.B.32200 |
0.358 |
|
| 2013 |
Zhao Z, Webb BT, Jia P, Bigdeli TB, Maher BS, van den Oord E, Bergen SE, Amdur RL, O'Neill FA, Walsh D, Thiselton DL, Chen X, Pato CN, Riley BP, et al. Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. Plos One. 8: e67776. PMID 23922650 DOI: 10.1371/Journal.Pone.0067776 |
0.347 |
|
| 2013 |
Murphy E, Hou L, Maher BS, Woldehawariat G, Kassem L, Akula N, Laje G, McMahon FJ. Race, genetic ancestry and response to antidepressant treatment for major depression. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 38: 2598-606. PMID 23827886 DOI: 10.1038/Npp.2013.166 |
0.356 |
|
| 2013 |
Benke KS, Wu Y, Fallin DM, Maher B, Palmer LJ. Strategy to control type I error increases power to identify genetic variation using the full biological trajectory. Genetic Epidemiology. 37: 419-30. PMID 23633177 DOI: 10.1002/Gepi.21733 |
0.303 |
|
| 2012 |
Webb BT, Guo AY, Maher BS, Zhao Z, van den Oord EJ, Kendler KS, Riley BP, Gillespie NA, Prescott CA, Middeldorp CM, Willemsen G, de Geus EJ, Hottenga JJ, Boomsma DI, Slagboom EP, et al. Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. European Journal of Human Genetics : Ejhg. 20: 1078-84. PMID 22473089 DOI: 10.1038/Ejhg.2012.47 |
0.417 |
|
| 2012 |
Fanous AH, Middleton FA, Gentile K, Amdur RL, Maher BS, Zhao Z, Sun J, Medeiros H, Carvalho C, Ferreira SR, Macedo A, Knowles JA, Azevedo MH, Pato MT, Pato CN. Genetic overlap of schizophrenia and bipolar disorder in a high-density linkage survey in the Portuguese Island population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 383-91. PMID 22461138 DOI: 10.1002/Ajmg.B.32041 |
0.418 |
|
| 2012 |
Vanyukov MM, Tarter RE, Kirillova GP, Kirisci L, Reynolds MD, Kreek MJ, Conway KP, Maher BS, Iacono WG, Bierut L, Neale MC, Clark DB, Ridenour TA. Common liability to addiction and "gateway hypothesis": theoretical, empirical and evolutionary perspective. Drug and Alcohol Dependence. 123: S3-17. PMID 22261179 DOI: 10.1016/J.Drugalcdep.2011.12.018 |
0.321 |
|
| 2012 |
Hill LD, Ewens KG, Maher BS, York TP, Legro RS, Dunaif A, Strauss JF. Catechol-O-methyltransferase (COMT) single nucleotide polymorphisms and haplotypes are not major risk factors for polycystic ovary syndrome. Molecular and Cellular Endocrinology. 350: 72-7. PMID 22178088 DOI: 10.1016/J.Mce.2011.11.022 |
0.356 |
|
| 2012 |
Nestadt G, Wang Y, Grados MA, Riddle MA, Greenberg BD, Knowles JA, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Piacentini J, Geller D, Pauls D, ... ... Maher B, et al. Homeobox genes in obsessive-compulsive disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 53-60. PMID 22095678 DOI: 10.1002/Ajmg.B.32001 |
0.439 |
|
| 2011 |
Bigdeli TB, Maher BS, Zhao Z, Oord EJ, Thiselton DL, Sun J, Webb BT, Amdur RL, Wormley B, O'Neill FA, Walsh D, Riley BP, Kendler KS, Fanous AH. Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness. Plos One. 6: e21440. PMID 22220189 DOI: 10.1371/Journal.Pone.0021440 |
0.405 |
|
| 2011 |
Hettema JM, Webb BT, Guo AY, Zhao Z, Maher BS, Chen X, An SS, Sun C, Aggen SH, Kendler KS, Kuo PH, Otowa T, Flint J, van den Oord EJ. Prioritization and association analysis of murine-derived candidate genes in anxiety-spectrum disorders. Biological Psychiatry. 70: 888-96. PMID 21871609 DOI: 10.1016/J.Biopsych.2011.07.012 |
0.42 |
|
| 2011 |
Maher BS, Vladimirov VI, Latendresse SJ, Thiselton DL, McNamee R, Kang M, Bigdeli TB, Chen X, Riley BP, Hettema JM, Chilcoat H, Heidbreder C, Muglia P, Murrelle EL, Dick DM, et al. The AVPR1A gene and substance use disorders: association, replication, and functional evidence. Biological Psychiatry. 70: 519-27. PMID 21514569 DOI: 10.1016/J.Biopsych.2011.02.023 |
0.389 |
|
| 2011 |
Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, et al. GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry. 16: 1117-29. PMID 20838396 DOI: 10.1038/Mp.2010.96 |
0.388 |
|
| 2011 |
Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, Georgieva L, Williams NM, Morris DW, Quinn EM, Giegling I, Ikeda M, Wood J, Lencz T, Hultman C, ... ... Maher BS, et al. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry. 16: 429-41. PMID 20368704 DOI: 10.1038/Mp.2010.36 |
0.4 |
|
| 2011 |
Hatemi PK, Gillespie NA, Eaves LJ, Maher BS, Webb BT, Heath AC, Medland SE, Smyth DC, Beeby HN, Gordon SD, Montgomery GW, Zhu G, Byrne EM, Martin NG. A genome-wide analysis of liberal and conservative political attitudes Journal of Politics. 73: 271-285. DOI: 10.1017/S0022381610001015 |
0.327 |
|
| 2011 |
Maher BS, Hughes HB, Zubenko GS. RE: Butler AW et al. 2010. A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12. Am J Med genet part B 153B(8):1465-1473 American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 156: 866-867. DOI: 10.1002/Ajmg.B.31224 |
0.31 |
|
| 2010 |
Bergen SE, Maher BS, Fanous AH, Kendler KS. Detection of susceptibility genes as modifiers due to subgroup differences in complex disease. European Journal of Human Genetics : Ejhg. 18: 960-4. PMID 20354561 DOI: 10.1038/Ejhg.2010.39 |
0.349 |
|
| 2010 |
Maher BS, Reimers MA, Riley BP, Kendler KS. Allelic heterogeneity in genetic association meta-analysis: an application to DTNBP1 and schizophrenia. Human Heredity. 69: 71-9. PMID 19996605 DOI: 10.1159/000264445 |
0.402 |
|
| 2010 |
Riley B, Thiselton D, Maher BS, Bigdeli T, Wormley B, McMichael GO, Fanous AH, Vladimirov V, O'Neill FA, Walsh D, Kendler KS. Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. Molecular Psychiatry. 15: 29-37. PMID 19844207 DOI: 10.1038/Mp.2009.109 |
0.368 |
|
| 2010 |
Fanous AH, Zhao Z, van den Oord EJ, Maher BS, Thiselton DL, Bergen SE, Wormley B, Bigdeli T, Amdur RL, O'Neill FA, Walsh D, Kendler KS, Riley BP. Association study of SNAP25 and schizophrenia in Irish family and case-control samples. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 663-74. PMID 19806613 DOI: 10.1002/Ajmg.B.31037 |
0.383 |
|
| 2010 |
Maher BS, Hughes HB, Zubenko WN, Zubenko GS. Genetic linkage of region containing the CREB1 gene to depressive disorders in families with recurrent, early-onset, major depression: a re-analysis and confirmation of sex-specific effect. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 10-6. PMID 19517574 DOI: 10.1002/Ajmg.B.30987 |
0.394 |
|
| 2010 |
Thiselton DL, Maher BS, Webb BT, Bigdeli TB, O'Neill FA, Walsh D, Kendler KS, Riley BP. Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS). American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 323-31. PMID 19475563 DOI: 10.1002/Ajmg.B.30982 |
0.385 |
|
| 2009 |
Riley B, Kuo PH, Maher BS, Fanous AH, Sun J, Wormley B, O'Neill FA, Walsh D, Zhao Z, Kendler KS. The dystrobrevin binding protein 1 (DTNBP1) gene is associated with schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample. Schizophrenia Research. 115: 245-53. PMID 19800201 DOI: 10.1016/J.Schres.2009.09.008 |
0.379 |
|
| 2009 |
Marazita ML, Lidral AC, Murray JC, Field LL, Maher BS, Goldstein McHenry T, Cooper ME, Govil M, Daack-Hirsch S, Riley B, Jugessur A, Felix T, Morene L, Mansilla MA, Vieira AR, et al. Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results. Human Heredity. 68: 151-70. PMID 19521098 DOI: 10.1159/000224636 |
0.326 |
|
| 2009 |
Vanyukov MM, Kirisci L, Moss L, Tarter RE, Reynolds MD, Maher BS, Kirillova GP, Ridenour T, Clark DB. Measurement of the risk for substance use disorders: phenotypic and genetic analysis of an index of common liability. Behavior Genetics. 39: 233-44. PMID 19377872 DOI: 10.1007/S10519-009-9269-9 |
0.394 |
|
| 2009 |
Vladimirov VI, Maher BS, Wormley B, O'Neill FA, Walsh D, Kendler KS, Riley BP. The trace amine associated receptor (TAAR6) gene is not associated with schizophrenia in the Irish Case-Control Study of Schizophrenia (ICCSS) sample. Schizophrenia Research. 107: 249-54. PMID 18973992 DOI: 10.1016/J.Schres.2008.09.030 |
0.335 |
|
| 2009 |
Vanyukov MM, Kirisci L, Moss L, Tarter RE, Reynolds MD, Maher BS, Kirillova GP, Ridenour T, Clark DB. Measurement of the risk for substance use disorders: Phenotypic and genetic analysis of an index of common liability (Behavior Genetics (2009) 39, (233-244) DOI: 10.1007/s10519-009-9269-9) Behavior Genetics. 39: 596. DOI: 10.1007/S10519-009-9292-X |
0.386 |
|
| 2008 |
Maher BS, Riley BP, Kendler KS. Psychiatric genetics gets a boost. Nature Genetics. 40: 1042-4. PMID 19165917 DOI: 10.1038/Ng0908-1042 |
0.408 |
|
| 2008 |
Weinberg SM, Neiswanger K, Richtsmeier JT, Maher BS, Mooney MP, Siegel MI, Marazita ML. Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: a possible marker for genetic susceptibility. American Journal of Medical Genetics. Part A. 146: 409-20. PMID 18203157 DOI: 10.1002/Ajmg.A.32177 |
0.318 |
|
| 2008 |
Chen X, Wang X, Chen Q, Williamson V, van den Oord E, Maher BS, O'Neill FA, Walsh D, Kendler KS. MEGF10 association with schizophrenia. Biological Psychiatry. 63: 441-8. PMID 18179784 DOI: 10.1016/J.Biopsych.2007.11.003 |
0.338 |
|
| 2007 |
Perdry H, Maher BS, Babron MC, McHenry T, Clerget-Darpoux F, Marazita ML. An ordered subset approach to including covariates in the transmission disequilibrium test. Bmc Proceedings. 1: S77. PMID 18466579 DOI: 10.1186/1753-6561-1-S1-S77 |
0.334 |
|
| 2007 |
Vanyukov MM, Maher BS, Devlin B, Kirillova GP, Kirisci L, Yu LM, Ferrell RE. The MAOA promoter polymorphism, disruptive behavior disorders, and early onset substance use disorder: gene-environment interaction. Psychiatric Genetics. 17: 323-32. PMID 18075472 DOI: 10.1097/Ypg.0B013E32811F6691 |
0.385 |
|
| 2007 |
Weinberg SM, Jenkins EA, Marazita ML, Maher BS. Minor physical anomalies in schizophrenia: a meta-analysis. Schizophrenia Research. 89: 72-85. PMID 17079117 DOI: 10.1016/J.Schres.2006.09.002 |
0.33 |
|
| 2007 |
Zubenko GS, Hughes HB, Zubenko WN, Maher BS. Genome survey for loci that influence successful aging: results at 10-cM resolution. The American Journal of Geriatric Psychiatry : Official Journal of the American Association For Geriatric Psychiatry. 15: 184-93. PMID 16905685 DOI: 10.1097/01.Jgp.0000231681.89741.Af |
0.37 |
|
| 2006 |
Jenkins EA, Maher BS, Marazita ML, Tarter RE, Ganger JB, Watt-Morse M, Vanyukov MM. Pittsburgh Registry of Infant Multiplets (PRIM): an update. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 9: 1006-8. PMID 17254444 DOI: 10.1375/183242706779462921 |
0.311 |
|
| 2006 |
Rand CM, Weese-Mayer DE, Maher BS, Zhou L, Marazita ML, Berry-Kravis EM. Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome. American Journal of Medical Genetics. Part A. 140: 1447-52. PMID 16763966 DOI: 10.1002/Ajmg.A.31306 |
0.313 |
|
| 2005 |
Cooper ME, Goldstein TH, Maher BS, Marazita ML. Identifying genomic regions for fine-mapping using genome scan meta-analysis (GSMA) to identify the minimum regions of maximum significance (MRMS) across populations. Bmc Genetics. 6: S42. PMID 16451653 DOI: 10.1186/1471-2156-6-S1-S42 |
0.327 |
|
| 2005 |
Brock GN, Maher BS, Goldstein TH, Cooper ME, Marazita ML. Methods for detecting gene x gene interaction in multiplex extended pedigrees. Bmc Genetics. 6: S144. PMID 16451604 DOI: 10.1186/1471-2156-6-S1-S144 |
0.333 |
|
| 2005 |
Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeböller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, et al. Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans. Bmc Genetics. 6: S1. PMID 16451554 DOI: 10.1186/1471-2156-6-S1-S1 |
0.356 |
|
| 2005 |
Maher BS, Brock GN. Approaches to detecting gene x gene interaction in Genetic Analysis Workshop 14 pedigrees. Genetic Epidemiology. 29: S116-9. PMID 16342178 DOI: 10.1002/Gepi.20119 |
0.356 |
|
| 2004 |
Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, Natsume N, Yoshiura K, Vieira AR, Orioli IM, Castilla EE, et al. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. The New England Journal of Medicine. 351: 769-80. PMID 15317890 DOI: 10.1056/Nejmoa032909 |
0.419 |
|
| 2004 |
Zubenko GS, Maher BS, Hughes HB, Zubenko WN, Scott Stiffler J, Marazita ML. Genome-wide linkage survey for genetic loci that affect the risk of suicide attempts in families with recurrent, early-onset, major depression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 129: 47-54. PMID 15274040 DOI: 10.1002/Ajmg.B.30092 |
0.43 |
|
| 2004 |
Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Curran ME, Silvestri JM, Marazita ML. Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Pediatric Research. 56: 391-5. PMID 15240857 DOI: 10.1203/01.Pdr.0000136285.91048.4A |
0.318 |
|
| 2004 |
Marazita ML, Murray JC, Lidral AC, Arcos-Burgos M, Cooper ME, Goldstein T, Maher BS, Daack-Hirsch S, Schultz R, Mansilla MA, Field LL, Liu YE, Prescott N, Malcolm S, Winter R, et al. Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. American Journal of Human Genetics. 75: 161-73. PMID 15185170 DOI: 10.1086/422475 |
0.378 |
|
| 2004 |
Moreno LM, Arcos-Burgos M, Marazita ML, Krahn K, Maher BS, Cooper ME, Valencia-Ramirez CR, Lidral AC. Genetic analysis of candidate loci in non-syndromic cleft lip families from Antioquia-Colombia and Ohio. American Journal of Medical Genetics. Part A. 125: 135-44. PMID 14981713 DOI: 10.1002/Ajmg.A.20425 |
0.305 |
|
| 2004 |
Vanyukov MM, Maher BS, Devlin B, Tarter RE, Kirillova GP, Yu LM, Ferrell RE. Haplotypes of the monoamine oxidase genes and the risk for substance use disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 120-5. PMID 14755456 DOI: 10.1002/Ajmg.B.20105 |
0.432 |
|
| 2003 |
Vanyukov MM, Kirisci L, Tarter RE, Simkevitz HF, Kirillova GP, Maher BS, Clark DB. Liability to substance use disorders: 2. A measurement approach. Neuroscience and Biobehavioral Reviews. 27: 517-26. PMID 14599433 DOI: 10.1016/J.Neubiorev.2003.08.003 |
0.374 |
|
| 2003 |
Vanyukov MM, Tarter RE, Kirisci L, Kirillova GP, Maher BS, Clark DB. Liability to substance use disorders: 1. Common mechanisms and manifestations. Neuroscience and Biobehavioral Reviews. 27: 507-15. PMID 14599432 DOI: 10.1016/J.Neubiorev.2003.08.002 |
0.382 |
|
| 2003 |
Zubenko GS, Maher B, Hughes HB, Zubenko WN, Stiffler JS, Kaplan BB, Marazita ML. Genome-wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early-onset, major depression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 123: 1-18. PMID 14582139 DOI: 10.1002/Ajmg.B.20073 |
0.446 |
|
| 2003 |
Weese-Mayer DE, Zhou L, Berry-Kravis EM, Maher BS, Silvestri JM, Marazita ML. Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis. American Journal of Medical Genetics. Part A. 122: 238-45. PMID 12966525 DOI: 10.1002/Ajmg.A.20427 |
0.366 |
|
| 2003 |
Zubenko GS, Hughes HB, Stiffler JS, Brechbiel A, Zubenko WN, Maher BS, Marazita ML. Sequence variations in CREB1 cosegregate with depressive disorders in women. Molecular Psychiatry. 8: 611-8. PMID 12851637 DOI: 10.1038/Sj.Mp.4001354 |
0.358 |
|
| 2003 |
El-Gheriani AA, Maher BS, El-Gheriani AS, Sciote JJ, Abu-Shahba FA, Al-Azemi R, Marazita ML. Segregation analysis of mandibular prognathism in Libya. Journal of Dental Research. 82: 523-7. PMID 12821712 DOI: 10.1177/154405910308200707 |
0.356 |
|
| 2003 |
Weese-Mayer DE, Berry-Kravis EM, Maher BS, Silvestri JM, Curran ME, Marazita ML. Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene. American Journal of Medical Genetics. Part A. 117: 268-74. PMID 12599191 DOI: 10.1002/Ajmg.A.20005 |
0.341 |
|
| 2002 |
Maher BS, Marazita ML, Zubenko WN, Kaplan BB, Zubenko GS. Genetic segregation analysis of alcohol and other substance-use disorders in families with recurrent, early-onset major depression. The American Journal of Drug and Alcohol Abuse. 28: 711-31. PMID 12492266 DOI: 10.1081/Ada-120015878 |
0.349 |
|
| 2002 |
Zubenko GS, Hughes HB, Maher BS, Stiffler JS, Zubenko WN, Marazita ML. Genetic linkage of region containing the CREB1 gene to depressive disorders in women from families with recurrent, early-onset, major depression. American Journal of Medical Genetics. 114: 980-7. PMID 12457397 DOI: 10.1002/Ajmg.B.10933 |
0.405 |
|
| 2002 |
Maher BS, Marazita ML, Ferrell RE, Vanyukov MM. Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis. Psychiatric Genetics. 12: 207-15. PMID 12454525 DOI: 10.1097/00041444-200212000-00003 |
0.325 |
|
| 2002 |
al-Bustan SA, el-Zawahri MM, al-Adsani AM, Bang RL, Ghunaim I, Maher BS, Weinberg S, Marazita ML. Epidemiological and genetic study of 121 cases of oral clefts in Kuwait. Orthodontics & Craniofacial Research. 5: 154-60. PMID 12194664 DOI: 10.1034/J.1600-0544.2002.02203.X |
0.331 |
|
| 2002 |
Marazita ML, Field LL, Cooper ME, Tobias R, Maher BS, Peanchitlertkajorn S, Liu YE. Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families. American Journal of Human Genetics. 71: 349-64. PMID 12087515 DOI: 10.1086/341944 |
0.329 |
|
| 2002 |
Marazita ML, Field LL, Cooper ME, Tobias R, Maher BS, Peanchitlertkajorn S, Liu YE. Nonsyndromic cleft lip with or without cleft palate in China: assessment of candidate regions. The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association. 39: 149-56. PMID 11879070 DOI: 10.1597/1545-1569(2002)039<0149:Nclwow>2.0.Co;2 |
0.347 |
|
| 2002 |
Maher BS, Marazita ML, Zubenko WN, Spiker DG, Giles DE, Kaplan BB, Zubenko GS. Genetic segregation analysis of recurrent, early-onset major depression: evidence for single major locus transmission. American Journal of Medical Genetics. 114: 214-21. PMID 11857584 DOI: 10.1002/Ajmg.10158 |
0.398 |
|
| 2001 |
Maher BS, Vanyukov MM, Cooper ME, Neiwswanger K, Marazita ML. Quantitative trait linkage analysis of the liability underlying a common oligogenic disease. Genetic Epidemiology. 21: S720-5. PMID 11793767 DOI: 10.1002/Gepi.2001.21.S1.S720 |
0.37 |
|
| 2001 |
Weese-Mayer DE, Silvestri JM, Huffman AD, Smok-Pearsall SM, Kowal MH, Maher BS, Cooper ME, Marazita ML. Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome. American Journal of Medical Genetics. 100: 237-45. PMID 11343310 DOI: 10.1002/Ajmg.1249 |
0.312 |
|
| 2001 |
Marazita ML, Maher BS, Cooper ME, Silvestri JM, Huffman AD, Smok-Pearsall SM, Kowal MH, Weese-Mayer DE. Genetic segregation analysis of autonomic nervous system dysfunction in families of probands with idiopathic congenital central hypoventilation syndrome. American Journal of Medical Genetics. 100: 229-36. PMID 11343309 DOI: 10.1002/Ajmg.1284 |
0.345 |
|
| 2001 |
Vanyukov MM, Maher BS, Ferrell RE, Devlin B, Marazita ML, Kirillova GP. Association between the Dopamine Receptor D5 Gene and the Liability to Substance Dependence in Males: A Replication Journal of Child and Adolescent Substance Abuse. 10: 55-63. DOI: 10.1300/J029V10N04_06 |
0.317 |
|
| 1999 |
Maher BS, Marazita ML, Moss HB, Vanyukov MM. Segregation analysis of attention deficit hyperactivity disorder. American Journal of Medical Genetics. 88: 71-8. PMID 10050971 DOI: 10.1002/(Sici)1096-8628(19990205)88:1<71::Aid-Ajmg13>3.0.Co;2-D |
0.34 |
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