| Year |
Citation |
Score |
| 2022 |
Yin X, Chan LS, Bose D, Jackson AU, VandeHaar P, Locke AE, Fuchsberger C, Stringham HM, Welch R, Yu K, Fernandes Silva L, Service SK, Zhang D, Hector EC, Young E, ... ... Freimer NB, et al. Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nature Communications. 13: 1644. PMID 35347128 DOI: 10.1038/s41467-022-29143-5 |
0.395 |
|
| 2021 |
Chen L, Abel HJ, Das I, Larson DE, Ganel L, Kanchi KL, Regier AA, Young EP, Kang CJ, Scott AJ, Chiang C, Wang X, Lu S, Christ R, Service SK, ... ... Freimer NB, et al. Association of structural variation with cardiometabolic traits in Finns. American Journal of Human Genetics. 108: 583-596. PMID 33798444 DOI: 10.1016/j.ajhg.2021.03.008 |
0.61 |
|
| 2020 |
Sul JH, Service SK, Huang AY, Ramensky V, Hwang SG, Teshiba TM, Park Y, Ori APS, Zhang Z, Mullins N, Olde Loohuis LM, Fears SC, Araya C, Araya X, Spesny M, ... ... Freimer NB, et al. Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates. Translational Psychiatry. 10: 74. PMID 32094344 DOI: 10.1038/S41398-020-0758-1 |
0.349 |
|
| 2019 |
Tabassum R, Rämö JT, Ripatti P, Koskela JT, Kurki M, Karjalainen J, Palta P, Hassan S, Nunez-Fontarnau J, Kiiskinen TTJ, Söderlund S, Matikainen N, Gerl MJ, Surma MA, Klose C, ... ... Freimer NB, et al. Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Nature Communications. 10: 4329. PMID 31551469 DOI: 10.1038/S41467-019-11954-8 |
0.338 |
|
| 2019 |
Locke AE, Steinberg KM, Chiang CWK, Service SK, Havulinna AS, Stell L, Pirinen M, Abel HJ, Chiang CC, Fulton RS, Jackson AU, Kang CJ, Kanchi KL, Koboldt DC, Larson DE, ... ... Freimer NB, et al. Exome sequencing of Finnish isolates enhances rare-variant association power. Nature. PMID 31367044 DOI: 10.1038/S41586-019-1457-Z |
0.356 |
|
| 2018 |
Savage JE, Jansen PR, Stringer S, Watanabe K, Bryois J, de Leeuw CA, Nagel M, Awasthi S, Barr PB, Coleman JRI, Grasby KL, Hammerschlag AR, Kaminski JA, Karlsson R, Krapohl E, ... ... Freimer NA, et al. Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Nature Genetics. PMID 29942086 DOI: 10.1038/S41588-018-0152-6 |
0.41 |
|
| 2017 |
Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, ... ... Freimer NB, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/J.Neuron.2017.06.010 |
0.314 |
|
| 2016 |
Ripatti P, Rämö JT, Söderlund S, Surakka I, Matikainen N, Pirinen M, Pajukanta P, Sarin AP, Service SK, Laurila PP, Ehnholm C, Salomaa V, Wilson RK, Palotie A, Freimer NB, et al. The Contribution of GWAS Loci in Familial Dyslipidemias. Plos Genetics. 12: e1006078. PMID 27227539 DOI: 10.1371/journal.pgen.1006078 |
0.326 |
|
| 2016 |
Peterson CB, Service SK, Jasinska AJ, Gao F, Zelaya I, Teshiba TM, Bearden CE, Cantor RM, Reus VI, Macaya G, López-Jaramillo C, Bogomolov M, Benjamini Y, Eskin E, Coppola G, ... Freimer NB, et al. Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder. Plos Genetics. 12: e1006046. PMID 27176483 DOI: 10.1371/Journal.Pgen.1006046 |
0.381 |
|
| 2015 |
Warren WC, Jasinska AJ, Garcia-Perez R, Svardal H, Tomlinson C, Rocchi M, Archidiacono N, Capozzi O, Minx P, Montague MJ, Kyung K, Hillier LW, Kremitzki M, Graves T, Chiang C, ... ... Freimer NB, et al. The genome of the vervet (Chlorocebus aethiops sabaeus). Genome Research. PMID 26377836 DOI: 10.1101/Gr.192922.115 |
0.32 |
|
| 2014 |
Lim ET, Würtz P, Havulinna AS, Palta P, Tukiainen T, Rehnström K, Esko T, Mägi R, Inouye M, Lappalainen T, Chan Y, Salem RM, Lek M, Flannick J, Sim X, ... ... Freimer NB, et al. Distribution and medical impact of loss-of-function variants in the Finnish founder population. Plos Genetics. 10: e1004494. PMID 25078778 DOI: 10.1371/Journal.Pgen.1004494 |
0.536 |
|
| 2014 |
Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, ... ... Freimer NB, et al. Genetic association signal near NTN4 in Tourette syndrome. Annals of Neurology. 76: 310-5. PMID 25042818 DOI: 10.1002/Ana.24215 |
0.348 |
|
| 2014 |
Fears SC, Service SK, Kremeyer B, Araya C, Araya X, Bejarano J, Ramirez M, Castrillón G, Gomez-Franco J, Lopez MC, Montoya G, Montoya P, Aldana I, Teshiba TM, Abaryan Z, ... ... Freimer NB, et al. Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. Jama Psychiatry. 71: 375-87. PMID 24522887 DOI: 10.1001/Jamapsychiatry.2013.4100 |
0.361 |
|
| 2014 |
Service SK, Teslovich TM, Fuchsberger C, Ramensky V, Yajnik P, Koboldt DC, Larson DE, Zhang Q, Lin L, Welch R, Ding L, McLellan MD, O'Laughlin M, Fronick C, Fulton LL, ... ... Freimer NB, et al. Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. Plos Genetics. 10: e1004147. PMID 24497850 DOI: 10.1371/Journal.Pgen.1004147 |
0.46 |
|
| 2013 |
Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, ... ... Freimer NB, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/Journal.Pgen.1003864 |
0.362 |
|
| 2013 |
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, Demirkan A, ... ... Freimer NB, et al. Discovery and refinement of loci associated with lipid levels. Nature Genetics. 45: 1274-83. PMID 24097068 DOI: 10.1038/Ng.2797 |
0.535 |
|
| 2013 |
Do R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, ... ... Freimer NB, et al. Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics. 45: 1345-52. PMID 24097064 DOI: 10.1038/Ng.2795 |
0.48 |
|
| 2012 |
McQuillan R, Eklund N, Pirastu N, Kuningas M, McEvoy BP, Esko T, Corre T, Davies G, Kaakinen M, Lyytikäinen LP, Kristiansson K, Havulinna AS, Gögele M, Vitart V, Tenesa A, ... ... Freimer N, et al. Evidence of inbreeding depression on human height. Plos Genetics. 8: e1002655. PMID 22829771 DOI: 10.1371/Journal.Pgen.1002655 |
0.391 |
|
| 2012 |
Levine AJ, Service S, Miller EN, Reynolds SM, Singer EJ, Shapshak P, Martin EM, Sacktor N, Becker JT, Jacobson LP, Thompson P, Freimer N. Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 669-83. PMID 22628157 DOI: 10.1002/Ajmg.B.32071 |
0.372 |
|
| 2012 |
Jasinska AJ, Lin MK, Service S, Choi OW, DeYoung J, Grujic O, Kong SY, Jung Y, Jorgensen MJ, Fairbanks LA, Turner T, Cantor RM, Wasserscheid J, Dewar K, Warren W, ... ... Freimer NB, et al. A non-human primate system for large-scale genetic studies of complex traits. Human Molecular Genetics. 21: 3307-16. PMID 22556363 DOI: 10.1093/Hmg/Dds160 |
0.393 |
|
| 2012 |
Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann Ø, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, ... ... Freimer NB, et al. Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics. 44: 552-61. PMID 22504417 DOI: 10.1038/Ng.2250 |
0.301 |
|
| 2012 |
Dastani Z, Hivert MF, Timpson N, Perry JR, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikäinen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, ... ... Freimer NB, et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607. PMID 22479202 DOI: 10.1371/Journal.Pgen.1002607 |
0.33 |
|
| 2012 |
Kettunen J, Tukiainen T, Sarin AP, Ortega-Alonso A, Tikkanen E, Lyytikäinen LP, Kangas AJ, Soininen P, Würtz P, Silander K, Dick DM, Rose RJ, Savolainen MJ, Viikari J, Kähönen M, ... ... Freimer NB, et al. Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Nature Genetics. 44: 269-76. PMID 22286219 DOI: 10.1038/Ng.1073 |
0.356 |
|
| 2011 |
Surakka I, Isaacs A, Karssen LC, Laurila PP, Middelberg RP, Tikkanen E, Ried JS, Lamina C, Mangino M, Igl W, Hottenga JJ, Lagou V, van der Harst P, Mateo Leach I, Esko T, ... ... Freimer NB, et al. A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. Plos Genetics. 7: e1002333. PMID 22028671 DOI: 10.1371/Journal.Pgen.1002333 |
0.412 |
|
| 2011 |
Wegmann D, Kessner DE, Veeramah KR, Mathias RA, Nicolae DL, Yanek LR, Sun YV, Torgerson DG, Rafaels N, Mosley T, Becker LC, Ruczinski I, Beaty TH, Kardia SL, Meyers DA, ... ... Freimer NB, et al. Recombination rates in admixed individuals identified by ancestry-based inference. Nature Genetics. 43: 847-53. PMID 21775992 DOI: 10.1038/Ng.894 |
0.516 |
|
| 2011 |
Pietiläinen OPH, Rehnström K, Jakkula E, Service SK, Congdon E, Tilgmann C, Hartikainen AL, Taanila A, Heikura U, Paunio T, Ripatti S, Jarvelin MR, Isohanni M, Sabatti C, Palotie A, ... Freimer NB, et al. Phenotype mining in CNV carriers from a population cohort Human Molecular Genetics. 20: 2686-2695. PMID 21505072 DOI: 10.1093/Hmg/Ddr162 |
0.399 |
|
| 2011 |
Dehghan A, Dupuis J, Barbalic M, Bis JC, Eiriksdottir G, Lu C, Pellikka N, Wallaschofski H, Kettunen J, Henneman P, Baumert J, Strachan DP, Fuchsberger C, Vitart V, Wilson JF, ... ... Freimer NB, et al. Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. Circulation. 123: 731-8. PMID 21300955 DOI: 10.1161/Circulationaha.110.948570 |
0.444 |
|
| 2010 |
Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Lango Allen H, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, ... ... Freimer NB, et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics. 42: 937-48. PMID 20935630 DOI: 10.1038/Ng.686 |
0.53 |
|
| 2010 |
Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Mägi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, ... ... Freimer NB, et al. Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics. 42: 949-60. PMID 20935629 DOI: 10.1038/Ng.685 |
0.514 |
|
| 2010 |
Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segrè AV, Speliotes EK, ... ... Freimer NB, et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 467: 832-8. PMID 20881960 DOI: 10.1038/Nature09410 |
0.576 |
|
| 2010 |
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, ... ... Freimer NB, et al. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 466: 707-13. PMID 20686565 DOI: 10.1038/Nature09270 |
0.379 |
|
| 2010 |
Widén E, Ripatti S, Cousminer DL, Surakka I, Lappalainen T, Järvelin MR, Eriksson JG, Raitakari O, Salomaa V, Sovio U, Hartikainen AL, Pouta A, McCarthy MI, Osmond C, Kajantie E, ... ... Freimer N, et al. Distinct variants at LIN28B influence growth in height from birth to adulthood. American Journal of Human Genetics. 86: 773-82. PMID 20398887 DOI: 10.1016/J.Ajhg.2010.03.010 |
0.474 |
|
| 2010 |
Kang HM, Sul JH, Service SK, Zaitlen NA, Kong SY, Freimer NB, Sabatti C, Eskin E. Variance component model to account for sample structure in genome-wide association studies. Nature Genetics. 42: 348-54. PMID 20208533 DOI: 10.1038/Ng.548 |
0.344 |
|
| 2010 |
Pillas D, Hoggart CJ, Evans DM, O'Reilly PF, Sipilä K, Lähdesmäki R, Millwood IY, Kaakinen M, Netuveli G, Blane D, Charoen P, Sovio U, Pouta A, Freimer N, Hartikainen AL, et al. Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. Plos Genetics. 6: e1000856. PMID 20195514 DOI: 10.1371/journal.pgen.1000856 |
0.326 |
|
| 2009 |
Chambers JC, Zhang W, Li Y, Sehmi J, Wass MN, Zabaneh D, Hoggart C, Bayele H, McCarthy MI, Peltonen L, Freimer NB, Srai SK, Maxwell PH, Sternberg MJ, Ruokonen A, et al. Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. Nature Genetics. 41: 1170-2. PMID 19820698 DOI: 10.1038/Ng.462 |
0.347 |
|
| 2009 |
Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D, Werge T, Pietiläinen OP, Mors O, Mortensen PB, Sigurdsson E, Gustafsson O, Nyegaard M, Tuulio-Henriksson A, Ingason A, ... ... Freimer NB, et al. Common variants conferring risk of schizophrenia. Nature. 460: 744-7. PMID 19571808 DOI: 10.1038/Nature08186 |
0.335 |
|
| 2009 |
Sovio U, Bennett AJ, Millwood IY, Molitor J, O'Reilly PF, Timpson NJ, Kaakinen M, Laitinen J, Haukka J, Pillas D, Tzoulaki I, Molitor J, Hoggart C, Coin LJ, Whittaker J, ... ... Freimer NB, et al. Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966. Plos Genetics. 5: e1000409. PMID 19266077 DOI: 10.1371/journal.pgen.1000409 |
0.374 |
|
| 2009 |
Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Penninx BW, Janssens AC, Wilson JF, Spector T, Martin NG, Pedersen NL, Kyvik KO, Kaprio J, Hofman A, ... Freimer NB, et al. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics. 41: 47-55. PMID 19060911 DOI: 10.1038/Ng.269 |
0.36 |
|
| 2009 |
Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, Brodsky J, Jones CG, Zaitlen NA, Varilo T, Kaakinen M, Sovio U, Ruokonen A, Laitinen J, Jakkula E, Coin L, ... ... Freimer NB, et al. Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nature Genetics. 41: 35-46. PMID 19060910 DOI: 10.1038/Ng.271 |
0.4 |
|
| 2009 |
Prokopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, Thorleifsson G, Loos RJ, Manning AK, Jackson AU, Aulchenko Y, Potter SC, Erdos MR, Sanna S, Hottenga JJ, Wheeler E, ... ... Freimer N, et al. Variants in MTNR1B influence fasting glucose levels. Nature Genetics. 41: 77-81. PMID 19060907 DOI: 10.1038/Ng.290 |
0.327 |
|
| 2009 |
Munafò MR, Freimer NB, Ng W, Ophoff R, Veijola J, Miettunen J, Järvelin MR, Taanila A, Flint J. 5-HTTLPR genotype and anxiety-related personality traits: a meta-analysis and new data. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 271-81. PMID 18546120 DOI: 10.1002/ajmg.b.30808 |
0.346 |
|
| 2008 |
Jakkula E, Rehnström K, Varilo T, Pietiläinen OP, Paunio T, Pedersen NL, deFaire U, Järvelin MR, Saharinen J, Freimer N, Ripatti S, Purcell S, Collins A, Daly MJ, Palotie A, et al. The genome-wide patterns of variation expose significant substructure in a founder population. American Journal of Human Genetics. 83: 787-94. PMID 19061986 DOI: 10.1016/J.Ajhg.2008.11.005 |
0.372 |
|
| 2008 |
Wang S, Ray N, Rojas W, Parra MV, Bedoya G, Gallo C, Poletti G, Mazzotti G, Hill K, Hurtado AM, Camrena B, Nicolini H, Klitz W, Barrantes R, Molina JA, ... Freimer NB, et al. Geographic patterns of genome admixture in latin American mestizos Plos Genetics. 4. PMID 18369456 DOI: 10.1371/Journal.Pgen.1000037 |
0.313 |
|
| 2007 |
Freimer NB, Service SK, Ophoff RA, Jasinska AJ, McKee K, Villeneuve A, Belisle A, Bailey JN, Breidenthal SE, Jorgensen MJ, Mann JJ, Cantor RM, Dewar K, Fairbanks LA. A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species. Proceedings of the National Academy of Sciences of the United States of America. 104: 15811-6. PMID 17884980 DOI: 10.1073/pnas.0707640104 |
0.328 |
|
| 2007 |
Chanock SJ, Manolio T, Boehnke M, Boerwinkle E, Hunter DJ, Thomas G, Hirschhorn JN, Abecasis G, Altshuler D, Bailey-Wilson JE, Brooks LD, Cardon LR, Daly M, Donnelly P, ... ... Freimer NB, et al. Replicating genotype-phenotype associations. Nature. 447: 655-60. PMID 17554299 DOI: 10.1038/447655A |
0.49 |
|
| 2006 |
Wang H, Lin CH, Service S, Chen Y, Freimer N, Sabatti C. Linkage disequilibrium and haplotype homozygosity in population samples genotyped at a high marker density. Human Heredity. 62: 175-89. PMID 17077642 DOI: 10.1159/000096599 |
0.331 |
|
| 2006 |
Keen-Kim D, Mathews CA, Reus VI, Lowe TL, Herrera LD, Budman CL, Gross-Tsur V, Pulver AE, Bruun RD, Erenberg G, Naarden A, Sabatti C, Freimer NB. Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. Human Molecular Genetics. 15: 3324-8. PMID 17035247 DOI: 10.1093/Hmg/Ddl408 |
0.351 |
|
| 2006 |
Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, ... ... Freimer N, et al. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nature Genetics. 38: 556-60. PMID 16582909 DOI: 10.1038/Ng1770 |
0.344 |
|
| 2004 |
Freimer N, Sabatti C. The use of pedigree, sib-pair and association studies of common diseases for genetic mapping and epidemiology. Nature Genetics. 36: 1045-51. PMID 15454942 DOI: 10.1038/Ng1433 |
0.372 |
|
| 2004 |
Glatt CE, Tampilic M, Christie C, DeYoung J, Freimer NB. Re-screening serotonin receptors for genetic variants identifies population and molecular genetic complexity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 124: 92-100. PMID 14681923 DOI: 10.1002/ajmg.b.20056 |
0.323 |
|
| 2003 |
Carvajal-Carmona LG, Ophoff R, Hartiala J, Molina J, Leon P, Ospina J, Bedoya G, Freimer N, Ruiz-Linares A. Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica. Human Genetics. 112: 534-541. PMID 12601469 DOI: 10.1007/S00439-002-0899-8 |
0.337 |
|
| 2002 |
Ophoff RA, Escamilla MA, Service SK, Spesny M, Meshi DB, Poon W, Molina J, Fournier E, Gallegos A, Mathews C, Neylan T, Batki SL, Roche E, Ramirez M, Silva S, ... ... Freimer NB, et al. Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate. American Journal of Human Genetics. 71: 565-74. PMID 12119601 DOI: 10.1086/342291 |
0.322 |
|
| 2002 |
Glatt CE, Freimer NB. Association analysis of candidate genes for neuropsychiatric disease: the perpetual campaign. Trends in Genetics : Tig. 18: 307-12. PMID 12044360 DOI: 10.1016/S0168-9525(02)02670-7 |
0.357 |
|
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