David Glahn - Related publications

Affiliations: 
Yale University School of Medicine, New Haven, CT 
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
2020 Elvsåshagen T, Bahrami S, van der Meer D, Agartz I, Alnæs D, Barch DM, Baur-Streubel R, Bertolino A, Beyer MK, Blasi G, Borgwardt S, Boye B, Buitelaar J, Bøen E, Celius EG, ... , et al. The genetic architecture of human brainstem structures and their involvement in common brain disorders. Nature Communications. 11: 4016. PMID 32782260 DOI: 10.1038/s41467-020-17376-1   
2020 Crouch DJM, Bodmer WF. Polygenic inheritance, GWAS, polygenic risk scores, and the search for functional variants. Proceedings of the National Academy of Sciences of the United States of America. 117: 18924-18933. PMID 32753378 DOI: 10.1073/pnas.2005634117   
2020 Zhao L, Batta I, Matloff W, O'Driscoll C, Hobel S, Toga AW. Neuroimaging PheWAS (Phenome-Wide Association Study): A Free Cloud-Computing Platform for Big-Data, Brain-Wide Imaging Association Studies. Neuroinformatics. PMID 32822005 DOI: 10.1007/s12021-020-09486-4   
2020 Li C, Wu D, Lu Q. Set-based genetic association and interaction tests for survival outcomes based on weighted V statistics. Genetic Epidemiology. PMID 32896012 DOI: 10.1002/gepi.22353   
2020 Zhao Y, Li T, Zhu H. Bayesian sparse heritability analysis with high-dimensional neuroimaging phenotypes. Biostatistics (Oxford, England). PMID 32948880 DOI: 10.1093/biostatistics/kxaa035   
2020 Hofer E, Roshchupkin GV, Adams HHH, Knol MJ, Lin H, Li S, Zare H, Ahmad S, Armstrong NJ, Satizabal CL, Bernard M, Bis JC, Gillespie NA, Luciano M, Mishra A, ... , et al. Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nature Communications. 11: 4796. PMID 32963231 DOI: 10.1038/s41467-020-18367-y   
2020 Trajanoska K, Seppala LJ, Medina-Gomez C, Hsu YH, Zhou S, van Schoor NM, de Groot LCPGM, Karasik D, Richards JB, Kiel DP, Uitterlinden AG, Perry JRB, van der Velde N, Day FR, Rivadeneira F. Genetic basis of falling risk susceptibility in the UK Biobank Study. Communications Biology. 3: 543. PMID 32999390 DOI: 10.1038/s42003-020-01256-x   
2020 Tada H, Fujino N, Nomura A, Nakanishi C, Hayashi K, Takamura M, Kawashiri MA. Personalized medicine for cardiovascular diseases. Journal of Human Genetics. PMID 32772049 DOI: 10.1038/s10038-020-0818-7   
2020 Ma C, Li X, Chen J, Li Z, Guan J, Li Y, Yin S, Shi Y. Association Analysis Between Common Variants of the Gene and Three Mental Disorders in the Han Chinese Population. Genetic Testing and Molecular Biomarkers. PMID 33001715 DOI: 10.1089/gtmb.2019.0096   
2020 Li Y, Wang F, Wu M, Ma S. Integrative functional linear model for genome-wide association studies with multiple traits. Biostatistics (Oxford, England). PMID 33040145 DOI: 10.1093/biostatistics/kxaa043   
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, ... , 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   
2020 Hebbar P, Abubaker JA, Abu-Farha M, Alsmadi O, Elkum N, Alkayal F, John SE, Channanath A, Iqbal R, Pitkaniemi J, Tuomilehto J, Sladek R, Al-Mulla F, Thanaraj TA. Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Human Genetics. PMID 32902719 DOI: 10.1007/s00439-020-02222-7   
2020 Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, et al. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry. PMID 33057169 DOI: 10.1038/s41380-020-00898-x   
2020 Crawford H, Scerif G, Wilde L, Beggs A, Stockton J, Sandhu P, Shelley L, Oliver C, McCleery J. Genetic modifiers in rare disorders: the case of fragile X syndrome. European Journal of Human Genetics : Ejhg. PMID 32862204 DOI: 10.1038/s41431-020-00711-x   
2020 LoPresti M, Beck DB, Duggal P, Cummings DAT, Solomon BD. The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human Literature. American Journal of Human Genetics. 107: 381-402. PMID 32814065 DOI: 10.1016/j.ajhg.2020.08.007   
2020 Akhatar J, Singh MP, Sharma A, Kaur H, Kaur N, Sharma S, Bharti B, Sardana VK, Banga SS. Association Mapping of Seed Quality Traits Under Varying Conditions of Nitrogen Application in L. Czern & Coss. Frontiers in Genetics. 11: 744. PMID 33088279 DOI: 10.3389/fgene.2020.00744   
2020 Maqsood A, Frome DK, Gibly RF, Larson JE, Patel NM, Sarwark JF. IS (Idiopathic Scoliosis) etiology: Multifactorial genetic research continues. A systematic review 1950 to 2017. Journal of Orthopaedics. 21: 421-426. PMID 32943828 DOI: 10.1016/j.jor.2020.08.005   
2020 Wright GEB, Caron NS, Ng B, Casal L, Casazza W, Xu X, Ooi J, Pouladi MA, Mostafavi S, Ross CJD, Hayden MR. Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease. Human Molecular Genetics. PMID 32898862 DOI: 10.1093/hmg/ddaa184   
2020 Groopman EE, Povysil G, Goldstein DB, Gharavi AG. Rare genetic causes of complex kidney and urological diseases. Nature Reviews. Nephrology. PMID 32807983 DOI: 10.1038/s41581-020-0325-2   
2020 Ma C, Li Y, Li X, Liu J, Luo XJ. Identification of a functional SNP rs7304782 at schizophrenia risk locus 12q24.31 and validation of its association with schiz ophrenia in Chinese populations. Psychiatry Research. 294: 113491. PMID 33070109 DOI: 10.1016/j.psychres.2020.113491   
2020 Trifu SC, Kohn B, Vlasie A, Patrichi BE. Genetics of schizophrenia (Review). Experimental and Therapeutic Medicine. 20: 3462-3468. PMID 32905096 DOI: 10.3892/etm.2020.8973   
2020 Cohen C, Figueiredo EA, Belangero PS, Andreoli CV, Leal MF, Ejnisman B. Genetic Aspects in Shoulder Disorders. Revista Brasileira De Ortopedia. 55: 537-542. PMID 33093716 DOI: 10.1055/s-0040-1702955   
2020 Kibe M, Nyaga C, Nair SK, Beyene Y, Das B, M SL, Bright JM, Makumbi D, Kinyua J, Olsen MS, Prasanna BM, Gowda M. Combination of Linkage Mapping, GWAS, and GP to Dissect the Genetic Basis of Common Rust Resistance in Tropical Maize Germplasm. International Journal of Molecular Sciences. 21. PMID 32899999 DOI: 10.3390/ijms21186518   
2020 Wainberg M, Magis AT, Earls JC, Lovejoy JC, Sinnott-Armstrong N, Omenn GS, Hood L, Price ND. Multiomic blood correlates of genetic risk identify presymptomatic disease alterations. Proceedings of the National Academy of Sciences of the United States of America. 117: 21813-21820. PMID 32817414 DOI: 10.1073/pnas.2001429117   
2020 Brown MA, Xu H, Li Z. Genetics and the axial spondyloarthritis spectrum. Rheumatology (Oxford, England). 59: iv58-iv66. PMID 33053195 DOI: 10.1093/rheumatology/keaa464   
2020 Mahmoudi E, Atkins JR, Quidé Y, Reay WR, Cairns HM, Fitzsimmons C, Carr VJ, Green MJ, Cairns MJ. The MIR137 VNTR rs58335419 Is Associated With Cognitive Impairment in Schizophrenia and Altered Cortical Morphology. Schizophrenia Bulletin. PMID 32910167 DOI: 10.1093/schbul/sbaa123   
2020 Tang B, Shi H, Alfredsson L, Klareskog L, Padyukov L, Jiang X. Obesity-related traits and the development of rheumatoid arthritis - evidence from genetic data. Arthritis & Rheumatology (Hoboken, N.J.). PMID 32964675 DOI: 10.1002/art.41517   
2020 Au PYB, Eaton A, Dyment DA. Genetic mechanisms of neurodevelopmental disorders. Handbook of Clinical Neurology. 173: 307-326. PMID 32958182 DOI: 10.1016/B978-0-444-64150-2.00024-1   
2020 Ouellette AR, Neuner SM, Dumitrescu L, Anderson LC, Gatti DM, Mahoney ER, Bubier JA, Churchill G, Peters L, Huentelman MJ, Herskowitz JH, Yang HS, Smith AN, Reitz C, Kunkle BW, ... , et al. Cross-Species Analyses Identify Dlgap2 as a Regulator of Age-Related Cognitive Decline and Alzheimer's Dementia. Cell Reports. 32: 108091. PMID 32877673 DOI: 10.1016/j.celrep.2020.108091   
2020 Seo GH, Kim T, Choi IH, Park JY, Lee J, Kim S, Won DG, Oh A, Lee Y, Choi J, Lee H, Kang HG, Cho HY, Cho MH, Kim YJ, et al. Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE. Clinical Genetics. PMID 32901917 DOI: 10.1111/cge.13848   
2020 Brown DW, Myers TA, Machiela MJ. PCAmatchR: a flexible R package for optimal case-control matching using weighted principal components. Bioinformatics (Oxford, England). PMID 32926120 DOI: 10.1093/bioinformatics/btaa784   
2020 Mhaske A, Dileep KV, Kumar M, Poojary M, Pandhare K, Zhang KYJ, Scaria V, Binukumar BK. ATP7A Clinical Genetics Resource - A comprehensive clinically annotated database and resource for genetic variants in ATP7A gene. Computational and Structural Biotechnology Journal. 18: 2347-2356. PMID 32994893 DOI: 10.1016/j.csbj.2020.08.021   
2020 Cheema H, Bertoli-Avella AM, Skrahina V, Anjum MN, Waheed N, Saeed A, Beetz C, Perez-Lopez J, Rocha ME, Alawbathani S, Pereira C, Hovakimyan M, Patric IRP, Paknia O, Ameziane N, et al. Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utility. Npj Genomic Medicine. 5: 44. PMID 33083013 DOI: 10.1038/s41525-020-00150-z   
2020 Zrzavy T, Leutmezer F, Kristoferitsch W, Kornek B, Schneider C, Rommer P, Berger T, Zimprich A. Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families. Genes. 11. PMID 32854198 DOI: 10.3390/genes11090988   
2020 Liang B, Wang Y, Lin N, Huang H, Chen L, Chen M, Yu D, Chen X, He D, Xu L. Single Nucleotide Polymorphism Array Analysis of 102 Patients with Developmental Delay and/or Intellectual Disability from Fujian, China. Clinica Chimica Acta; International Journal of Clinical Chemistry. PMID 32858057 DOI: 10.1016/j.cca.2020.08.032   
2020 Wang X, Lim E, Liu CT, Sung YJ, Rao DC, Morrison AC, Boerwinkle E, Manning AK, Chen H. Efficient gene-environment interaction tests for large biobank-scale sequencing studies. Genetic Epidemiology. PMID 32864785 DOI: 10.1002/gepi.22351   
2020 Mullins VA, Bresette W, Johnstone L, Hallmark B, Chilton FH. Genomics in Personalized Nutrition: Can You "Eat for Your Genes"? Nutrients. 12. PMID 33065985 DOI: 10.3390/nu12103118   
2020 Roberson-Nay R, Lapato DM, Wolen AR, Lancaster EE, Webb BT, Verhulst B, Hettema JM, York TP. An epigenome-wide association study of early-onset major depression in monozygotic twins. Translational Psychiatry. 10: 301. PMID 32843619 DOI: 10.1038/s41398-020-00984-2   
2020 Olvany JM, Sausville LN, White MJ, Tacconelli A, Tavera G, Sobota RS, Ciccacci C, Bohlbro AS, Wejse C, Williams SM, Sirugo G. CLEC4E (Mincle) genetic variation associates with pulmonary tuberculosis in Guinea-Bissau (West Africa). Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases. 104560. PMID 32971250 DOI: 10.1016/j.meegid.2020.104560   
2020 Mulvey B, Lagunas T, Dougherty JD. Massively Parallel Reporter Assays: Defining Functional Psychiatric Genetic Variants Across Biological Contexts. Biological Psychiatry. PMID 32843144 DOI: 10.1016/j.biopsych.2020.06.011   
2020 Vuckovic D, Bao EL, Akbari P, Lareau CA, Mousas A, Jiang T, Chen MH, Raffield LM, Tardaguila M, Huffman JE, Ritchie SC, Megy K, Ponstingl H, Penkett CJ, Albers PK, ... , et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 182: 1214-1231.e11. PMID 32888494 DOI: 10.1016/j.cell.2020.08.008   
2020 Cavani L, Braz CU, Giglioti R, Okino CH, Gulias-Gomes CC, Caetano AR, Oliveira MCS, Cardoso FF, de Oliveira HN. Genomic Study of Infection Level and Its Association With Tick Count in Hereford and Braford Cattle. Frontiers in Immunology. 11: 1905. PMID 33013839 DOI: 10.3389/fimmu.2020.01905   
2020 Rau CD, Gonzales NM, Bloom JS, Park D, Ayroles J, Palmer AA, Lusis AJ, Zaitlen N. Modeling epistasis in mice and yeast using the proportion of two or more distinct genetic backgrounds: Evidence for "polygenic epistasis". Plos Genetics. 16: e1009165. PMID 33104702 DOI: 10.1371/journal.pgen.1009165   
2020 Owen KA, Price A, Ainsworth H, Aidukaitis BN, Bachali P, Catalina MD, Dittman JM, Howard TD, Kingsmore KM, Labonte AC, Marion MC, Robl RD, Zimmerman KD, Langefeld CD, Grammer AC, et al. Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries. American Journal of Human Genetics. PMID 33031749 DOI: 10.1016/j.ajhg.2020.09.007   
2020 Chhetri HB, Furches A, Macaya-Sanz D, Walker AR, Kainer D, Jones P, Harman-Ware AE, Tschaplinski TJ, Jacobson D, Tuskan GA, DiFazio SP. Genome-Wide Association Study of Wood Anatomical and Morphological Traits in . Frontiers in Plant Science. 11: 545748. PMID 33013968 DOI: 10.3389/fpls.2020.545748   
2020 Mata-Nicolás E, Montero-Pau J, Gimeno-Paez E, Garcia-Carpintero V, Ziarsolo P, Menda N, Mueller LA, Blanca J, Cañizares J, van der Knaap E, Díez MJ. Exploiting the diversity of tomato: the development of a phenotypically and genetically detailed germplasm collection. Horticulture Research. 7: 66. PMID 32377357 DOI: 10.1038/s41438-020-0291-7   
2020 Umehara H, Nakamura M, Nagai M, Kato Y, Ueno SI, Sano A. Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation. Journal of Human Genetics. PMID 32920599 DOI: 10.1038/s10038-020-00840-7   
2020 Umehara H, Nakamura M, Nagai M, Kato Y, Ueno SI, Sano A. Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation. Journal of Human Genetics. PMID 32920599 DOI: 10.1038/s10038-020-00840-7   
2020 León-Reyes G, Rivera-Paredez B, López JCF, Ramírez-Salazar EG, Aquino-Gálvez A, Gallegos-Carrillo K, Denova-Gutiérrez E, Salmerón J, Velázquez-Cruz R. The Variant rs1784042 of the Gene is Associated with Metabolic Syndrome through Low HDL-c Levels in a Mexican Population. Genes. 11. PMID 33066450 DOI: 10.3390/genes11101192   
2020 Grama S, Willcocks I, Hubert JJ, Pardiñas AF, Legge SE, Bracher-Smith M, Menzies GE, Hall LS, Pocklington AJ, Anney RJL, Bray NJ, Escott-Price V, Caseras X. Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort. Translational Psychiatry. 10: 309. PMID 32908133 DOI: 10.1038/s41398-020-00940-0