 Connection
Matthew Keller to Phenotype
This is a "connection" page, showing publications Matthew Keller has written about Phenotype.
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Connection Strength |
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1.782 |
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Cannon TD, Keller MC. Endophenotypes in the genetic analyses of mental disorders. Annu Rev Clin Psychol. 2006; 2:267-90.
Score: 0.149
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Grotzinger AD, Keller MC. Potential bias in genetic correlations. Science. 2022 11 18; 378(6621):709-710.
Score: 0.120
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Border R, O'Rourke S, de Candia T, Goddard ME, Visscher PM, Yengo L, Jones M, Keller MC. Assortative mating biases marker-based heritability estimators. Nat Commun. 2022 02 03; 13(1):660.
Score: 0.114
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Yengo L, Yang J, Keller MC, Goddard ME, Wray NR, Visscher PM. Genomic partitioning of inbreeding depression in humans. Am J Hum Genet. 2021 08 05; 108(8):1488-1501.
Score: 0.109
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Evans LM, Jang S, Hancock DB, Ehringer MA, Otto JM, Vrieze SI, Keller MC. Genetic architecture of four smoking behaviors using partitioned SNP heritability. Addiction. 2021 09; 116(9):2498-2508.
Score: 0.107
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Balbona JV, Kim Y, Keller MC. Estimation of Parental Effects Using Polygenic Scores. Behav Genet. 2021 05; 51(3):264-278.
Score: 0.106
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Kim Y, Balbona JV, Keller MC. Bias and Precision of Parameter Estimates from Models Using Polygenic Scores to Estimate Environmental and Genetic Parental Influences. Behav Genet. 2021 05; 51(3):279-288.
Score: 0.105
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Border R, Johnson EC, Evans LM, Smolen A, Berley N, Sullivan PF, Keller MC. No Support for Historical Candidate Gene or Candidate Gene-by-Interaction Hypotheses for Major Depression Across Multiple Large Samples. Am J Psychiatry. 2019 05 01; 176(5):376-387.
Score: 0.093
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Johnson EC, Evans LM, Keller MC. Relationships between estimated autozygosity and complex traits in the UK Biobank. PLoS Genet. 2018 07; 14(7):e1007556.
Score: 0.089
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Evans LM, Tahmasbi R, Vrieze SI, Abecasis GR, Das S, Gazal S, Bjelland DW, de Candia TR, Goddard ME, Neale BM, Yang J, Visscher PM, Keller MC. Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits. Nat Genet. 2018 05; 50(5):737-745.
Score: 0.088
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Evans LM, Keller MC. Using partitioned heritability methods to explore genetic architecture. Nat Rev Genet. 2018 02 14; 19(3):185.
Score: 0.086
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Border R, Keller MC. Commentary: Fundamental problems with candidate gene-by-environment interaction studies - reflections on Moore and Thoemmes (2016). J Child Psychol Psychiatry. 2017 03; 58(3):328-330.
Score: 0.081
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Palmer RH, Brick L, Nugent NR, Bidwell LC, McGeary JE, Knopik VS, Keller MC. Examining the role of common genetic variants on alcohol, tobacco, cannabis and illicit drug dependence: genetics of vulnerability to drug dependence. Addiction. 2015 Mar; 110(3):530-7.
Score: 0.070
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Keller MC, Medland SE, Duncan LE. Are extended twin family designs worth the trouble? A comparison of the bias, precision, and accuracy of parameters estimated in four twin family models. Behav Genet. 2010 May; 40(3):377-93.
Score: 0.049
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Keller MC, Medland SE, Duncan LE, Hatemi PK, Neale MC, Maes HH, Eaves LJ. Modeling extended twin family data I: description of the Cascade model. Twin Res Hum Genet. 2009 Feb; 12(1):8-18.
Score: 0.046
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Keller MC, Coventry WL. Quantifying and addressing parameter indeterminacy in the classical twin design. Twin Res Hum Genet. 2005 Jun; 8(3):201-13.
Score: 0.036
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Colbert SM, Keller MC, Agrawal A, Johnson EC. Exploring the Relationships Between Autozygosity, Educational Attainment, and Cognitive Ability in a Contemporary, Trans-Ancestral American Sample. Behav Genet. 2022 11; 52(6):315-323.
Score: 0.030
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Axelrud LK, Hoffmann MS, Vosberg DE, Santoro M, Pan PM, Gadelha A, Belangero SI, Miguel EC, Shin J, Thapar A, Smoller JW, Pausova Z, Rohde LA, Keller MC, Paus T, Salum GA. Disentangling the influences of parental genetics on offspring's cognition, education, and psychopathology via genetic and phenotypic pathways. J Child Psychol Psychiatry. 2023 03; 64(3):408-416.
Score: 0.030
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Jang SK, Evans L, Fialkowski A, Arnett DK, Ashley-Koch AE, Barnes KC, Becker DM, Bis JC, Blangero J, Bleecker ER, Boorgula MP, Bowden DW, Brody JA, Cade BE, Jenkins BWC, Carson AP, Chavan S, Cupples LA, Custer B, Damrauer SM, David SP, de Andrade M, Dinardo CL, Fingerlin TE, Fornage M, Freedman BI, Garrett ME, Gharib SA, Glahn DC, Haessler J, Heckbert SR, Hokanson JE, Hou L, Hwang SJ, Hyman MC, Judy R, Justice AE, Kaplan RC, Kardia SLR, Kelly S, Kim W, Kooperberg C, Levy D, Lloyd-Jones DM, Loos RJF, Manichaikul AW, Gladwin MT, Martin LW, Nouraie M, Melander O, Meyers DA, Montgomery CG, North KE, Oelsner EC, Palmer ND, Payton M, Peljto AL, Peyser PA, Preuss M, Psaty BM, Qiao D, Rader DJ, Rafaels N, Redline S, Reed RM, Reiner AP, Rich SS, Rotter JI, Schwartz DA, Shadyab AH, Silverman EK, Smith NL, Smith JG, Smith AV, Smith JA, Tang W, Taylor KD, Telen MJ, Vasan RS, Gordeuk VR, Wang Z, Wiggins KL, Yanek LR, Yang IV, Young KA, Young KL, Zhang Y, Liu DJ, Keller MC, Vrieze S. Rare genetic variants explain missing heritability in smoking. Nat Hum Behav. 2022 11; 6(11):1577-1586.
Score: 0.029
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Howe LJ, Nivard MG, Morris TT, Hansen AF, Rasheed H, Cho Y, Chittoor G, Ahlskog R, Lind PA, Palviainen T, van der Zee MD, Cheesman R, Mangino M, Wang Y, Li S, Klaric L, Ratliff SM, Bielak LF, Nygaard M, Giannelis A, Willoughby EA, Reynolds CA, Balbona JV, Andreassen OA, Ask H, Baras A, Bauer CR, Boomsma DI, Campbell A, Campbell H, Chen Z, Christofidou P, Corfield E, Dahm CC, Dokuru DR, Evans LM, de Geus EJC, Giddaluru S, Gordon SD, Harden KP, Hill WD, Hughes A, Kerr SM, Kim Y, Kweon H, Latvala A, Lawlor DA, Li L, Lin K, Magnus P, Magnusson PKE, Mallard TT, Martikainen P, Mills MC, Nj?lstad PR, Overton JD, Pedersen NL, Porteous DJ, Reid J, Silventoinen K, Southey MC, Stoltenberg C, Tucker-Drob EM, Wright MJ, Hewitt JK, Keller MC, Stallings MC, Lee JJ, Christensen K, Kardia SLR, Peyser PA, Smith JA, Wilson JF, Hopper JL, H?gg S, Spector TD, Pingault JB, Plomin R, Havdahl A, Bartels M, Martin NG, Oskarsson S, Justice AE, Millwood IY, Hveem K, Naess ?, Willer CJ, ?svold BO, Koellinger PD, Kaprio J, Medland SE, Walters RG, Benjamin DJ, Turley P, Evans DM, Davey Smith G, Hayward C, Brumpton B, Hemani G, Davies NM. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Nat Genet. 2022 05; 54(5):581-592.
Score: 0.029
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Wainberg M, Merico D, Keller MC, Fauman EB, Tripathy SJ. Predicting causal genes from psychiatric genome-wide association studies using high-level etiological knowledge. Mol Psychiatry. 2022 07; 27(7):3095-3106.
Score: 0.029
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Kemper KE, Yengo L, Zheng Z, Abdellaoui A, Keller MC, Goddard ME, Wray NR, Yang J, Visscher PM. Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals. Nat Commun. 2021 02 16; 12(1):1050.
Score: 0.027
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Evans LM, Johnson EC, Melroy-Greif WE, Hewitt JK, Hoeffer CA, Keller MC, Saba LM, Stitzel JA, Ehringer MA. The Role of A Priori-Identified Addiction and Smoking Gene Sets in Smoking Behaviors. Nicotine Tob Res. 2020 07 16; 22(8):1310-1315.
Score: 0.026
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Palmer RHC, Brick LA, Chou YL, Agrawal A, McGeary JE, Heath AC, Bierut L, Keller MC, Johnson E, Hartz SM, Schuckit MA, Knopik VS. The etiology of DSM-5 alcohol use disorder: Evidence of shared and non-shared additive genetic effects. Drug Alcohol Depend. 2019 08 01; 201:147-154.
Score: 0.024
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Liu M, Jiang Y, Wedow R, Li Y, Brazel DM, Chen F, Datta G, Davila-Velderrain J, McGuire D, Tian C, Zhan X, Choquet H, Docherty AR, Faul JD, Foerster JR, Fritsche LG, Gabrielsen ME, Gordon SD, Haessler J, Hottenga JJ, Huang H, Jang SK, Jansen PR, Ling Y, M?gi R, Matoba N, McMahon G, Mulas A, Orr? V, Palviainen T, Pandit A, Reginsson GW, Skogholt AH, Smith JA, Taylor AE, Turman C, Willemsen G, Young H, Young KA, Zajac GJM, Zhao W, Zhou W, Bjornsdottir G, Boardman JD, Boehnke M, Boomsma DI, Chen C, Cucca F, Davies GE, Eaton CB, Ehringer MA, Esko T, Fiorillo E, Gillespie NA, Gudbjartsson DF, Haller T, Harris KM, Heath AC, Hewitt JK, Hickie IB, Hokanson JE, Hopfer CJ, Hunter DJ, Iacono WG, Johnson EO, Kamatani Y, Kardia SLR, Keller MC, Kellis M, Kooperberg C, Kraft P, Krauter KS, Laakso M, Lind PA, Loukola A, Lutz SM, Madden PAF, Martin NG, McGue M, McQueen MB, Medland SE, Metspalu A, Mohlke KL, Nielsen JB, Okada Y, Peters U, Polderman TJC, Posthuma D, Reiner AP, Rice JP, Rimm E, Rose RJ, Runarsdottir V, Stallings MC, Stanc?kov? A, Stefansson H, Thai KK, Tindle HA, Tyrfingsson T, Wall TL, Weir DR, Weisner C, Whitfield JB, Winsvold BS, Yin J, Zuccolo L, Bierut LJ, Hveem K, Lee JJ, Munaf? MR, Saccone NL, Willer CJ, Cornelis MC, David SP, Hinds DA, Jorgenson E, Kaprio J, Stitzel JA, Stefansson K, Thorgeirsson TE, Abecasis G, Liu DJ, Vrieze S. Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Nat Genet. 2019 02; 51(2):237-244.
Score: 0.023
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Evans LM, Tahmasbi R, Jones M, Vrieze SI, Abecasis GR, Das S, Bjelland DW, de Candia TR, Yang J, Goddard ME, Visscher PM, Keller MC. Narrow-sense heritability estimation of complex traits using identity-by-descent information. Heredity (Edinb). 2018 12; 121(6):616-630.
Score: 0.022
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Demmitt BA, Corley RP, Huibregtse BM, Keller MC, Hewitt JK, McQueen MB, Knight R, McDermott I, Krauter KS. Genetic influences on the human oral microbiome. BMC Genomics. 2017 Aug 24; 18(1):659.
Score: 0.021
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Derringer J, Corley RP, Haberstick BC, Young SE, Demmitt BA, Howrigan DP, Kirkpatrick RM, Iacono WG, McGue M, Keller MC, Brown S, Tapert S, Hopfer CJ, Stallings MC, Crowley TJ, Rhee SH, Krauter K, Hewitt JK, McQueen MB. Genome-Wide Association Study of Behavioral Disinhibition in a Selected Adolescent Sample. Behav Genet. 2015 Jul; 45(4):375-81.
Score: 0.018
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Verweij KJ, Abdellaoui A, Veijola J, Sebert S, Koiranen M, Keller MC, J?rvelin MR, Zietsch BP. The association of genotype-based inbreeding coefficient with a range of physical and psychological human traits. PLoS One. 2014; 9(7):e103102.
Score: 0.017
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Maes HH, Neale MC, Medland SE, Keller MC, Martin NG, Heath AC, Eaves LJ. Flexible Mx specification of various extended twin kinship designs. Twin Res Hum Genet. 2009 Feb; 12(1):26-34.
Score: 0.012
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Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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