Karen L Mohlke

UNCCH, School of Medicine, Genetics

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Karen L Mohlke

• Organizations
  University of North Carolina at Chapel Hill
  
  School of Medicine
  
  Genetics
  
  

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This is a list of publications by this researcher, listed chronologically starting with the most recent first. New publications appear in this list weekly. The source of publications and 'cited by' data for this application is Scopus.

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• 1.

  2013

  Qing Duan; Eric Yi Liu; Damien C. Croteau-Chonka; Karen L. Mohlke; Yun Li

  A comprehensive SNP and indel imputability database

  Bioinformatics. 2013;29(4):528-531.
  0

• 2.

  2013

  Jeroen R. Huyghe; Anne U. Jackson; Marie P. Fogarty; Martin L. Buchkovich; Alena Stančáková; Heather M. Stringham; Xueling Sim; Lingyao Yang; Christian Fuchsberger; Henna Cederberg; et al.

  Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

  Nature Genetics. 2013;45(2):197-201.
  1

• 3.

  2013

  Momoko Horikoshi; Hanieh Yaghootkar; Dennis O Mook-Kanamori; Ulla Sovio; H Rob Taal; Branwen J Hennig; Jonathan P Bradfield; Beate St Pourcain; David M Evans; Pimphen Charoen; et al.

  New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

  Nature Genetics. 2013;45(1):76-82.
  0

• 4.

  2012

  Karen L. Mohlke; Laura J. Scott

  What will diabetes genomes tell us?

  Current Diabetes Reports. 2012;12(6):643-650.
  1

• 5.

  2012

  Jian Yang; Ruth J. F. Loos; Joseph E. Powell; Sarah E. Medland; Elizabeth K. Speliotes; Daniel I. Chasman; Lynda M. Rose; Gudmar Thorleifsson; Valgerdur Steinthorsdottir; Reedik Mägi; et al.

  FTO genotype is associated with phenotypic variability of body mass index

  Nature. 2012;490(7419):267-273.
  7

• 6.

  2012

  Andrew P. Morris; Benjamin F. Voight; Tanya M. Teslovich; Teresa Ferreira; Ayellet V. Segrè; Valgerdur Steinthorsdottir; Rona J. Strawbridge; Hassan Khan; Harald Grallert; Anubha Mahajan; et al.

  Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

  Nature Genetics. 2012;44(9):981-990.
  24

• 7.

  2012

  Robert A. Scott; Vasiliki Lagou; Ryan P. Welch; Eleanor Wheeler; May E. Montasser; Jian'An Luan; Reedik MäGi; Rona J. Strawbridge; Emil Rehnberg; Stefan Gustafsson; et al.

  Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

  Nature Genetics. 2012;44(9):991-1005.
  8

• 8.

  2012

  Christy L. Avery; Praveen Sethupathy; Steven Buyske; Qianchuan He; Dan-Yu Lin; Dan E. Arking; Cara L. Carty; David Duggan; Megan D. Fesinmeyer; Lucia A. Hindorff; et al.

  Fine-Mapping and Initial Characterization of QT Interval Loci in African Americans

  PLoS Genetics. 2012;8(8).
  0

• 9.

  2012

  Benjamin F. Voight; Gina M. Peloso; Marju Orho-Melander; Ruth Frikke-Schmidt; Maja Barbalic; Majken K. Jensen; George Hindy; Hilma Hólm; Eric L. Ding; Toby Johnson; et al.

  Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study

  The Lancet. 2012;380(9841):572-580.
  64

• 10.

  2012

  Alisa K. Manning; Marie-France Hivert; Robert A. Scott; Jonna L. Grimsby; Nabila Bouatia-Naji; Han Chen; Denis Rybin; Ching-Ti Liu; Lawrence F. Bielak; Inga Prokopenko; et al.

  A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

  Nature Genetics. 2012;44(6):659-669.
  17

• 11.

  2012

  John R. B. Perry; Benjamin F. Voight; Loïc Yengo; Najaf Amin; Josée Dupuis; Martha Ganser; Harald Grallert; Pau Navarro; Man Li; Lu Qi; et al.

  Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

  PLoS Genetics. 2012;8(5).
  7

• 12.

  2012

  H. Rob Taal; Beate St Pourcain; Elisabeth Thiering; Shikta Das; Dennis O. Mook-Kanamori; Nicole M. Warrington; Marika Kaakinen; Eskil Kreiner-Møller; Jonathan P. Bradfield; Rachel M. Freathy; et al.

  Common variants at 12q15 and 12q24 are associated with infant head circumference

  Nature Genetics. 2012;44(5):532-538.
  8

• 13.

  2012

  M. Arfan Ikram; Myriam Fornage; Albert V. Smith; Sudha Seshadri; Reinhold Schmidt; Stéphanie Debette; Henri A. Vrooman; Sigurdur Sigurdsson; Stefan Ropele; H. Rob Taal; et al.

  Common variants at 6q22 and 17q21 are associated with intracranial volume

  Nature Genetics. 2012;44(5):539-544.
  9

• 14.

  2012

  Steven Buyske; Ying Wu; Cara L. Carty; Iona Cheng; Themistocles L. Assimes; Logan Dumitrescu; Lucia A. Hindorff; Sabrina Mitchell; Jose Luis Ambite; Eric Boerwinkle; et al.

  Evaluation of the metabochip genotyping array in african americans and implications for fine mapping of gwas-identified loci: The PAGE study

  PLoS ONE. 2012;7(4).
  7

• 15.

  2012

  Ying Wu; Thomas W. McDade; Christopher W. Kuzawa; Judith Borja; Yun Li; Linda S. Adair; Karen L. Mohlke; Leslie A. Lange

  Genome-wide association with C-reactive protein levels in CLHNS: Evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment

  Inflammation. 2012;35(2):574-583.
  4

• 16.

  2012

  Cristen J. Willer; Karen L. Mohlke

  Finding genes and variants for lipid levels after genome-wide association analysis

  Current Opinion in Lipidology. 2012;23(2):98-103.
  4

• 17.

  2012

  Zari Dastani; Marie-France Hivert; Nicholas Timpson; John R. B. Perry; Xin Yuan; Robert A. Scott; Peter Henneman; Iris M. Heid; Jorge R. Kizer; Leo-Pekka Lyytikäinen; 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. 2012;8(3).
  13

• 18.

  2012

  Yoon Shin Cho; Chien-Hsiun Chen; Cheng Hu; Jirong Long; Rick Twee Hee Ong; Xueling Sim; Fumihiko Takeuchi; Ying Wu; Min Jin Go; Toshimasa Yamauchi; et al.

  Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

  Nature Genetics. 2012;44(1):67-72.
  40

• 19.

  2012

  Damien C. Croteau-chonka; Ying Wu; Yun Li; Marie P. Fogarty; Leslie A. Lange; Christopher W. Kuzawa; Thomas W. McDade; Judith B. Borja; Jingchun Luo; Omar AbdelBaky; et al.

  Population-specific coding variant underlies genome-wide association with adiponectin level

  Human Molecular Genetics. 2012;21(2):463-471.
  4

• 20.

  2011

  Ghenadie Curocichin; Ying Wu; Thomas W. McDade; Christopher W. Kuzawa; Judith B. Borja; Li Qin; Ethan M. Lange; Linda S. Adair; Leslie A. Lange; Karen L. Mohlke

  Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults

  Journal of Human Genetics. 2011;56(12):823-827.
  1

• 21.

  2011

  Iris M. Heid; Anne U. Jackson; Joshua C. Randall; Thomas W. Winkler; Lu Qi; Valgerdur Steinthorsdottir; Gudmar Thorleifsson; M. Carola Zillikens; Elizabeth K. Speliotes; Reedik Mägi; et al.

  Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (Nature Genetics (2010) 42 (949-960))

  Nature Genetics. 2011;43(11):1164.
  0

• 22.

  2011

  Tuomas O. Kilpeläinen; Lu Qi; Soren Brage; Stephen J. Sharp; Emily Sonestedt; Ellen Demerath; Tariq Ahmad; Samia Mora; Marika Kaakinen; Camilla Helene Sandholt; et al.

  Physical activity attenuates the influence of FTO variants on obesity risk: A meta-analysis of 218,166 adults and 19,268 children

  PLoS Medicine. 2011;8(11).
  32

• 23.

  2011

  Georg B. Ehret; Patricia B. Munroe; Kenneth M. Rice; Murielle Bochud; Andrew D. Johnson; Daniel I. Chasman; Albert V. Smith; Martin D. Tobin; Germaine C. Verwoert; Shih-Jen Hwang; et al.

  Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

  Nature. 2011;478(7367):103-109.
  153

• 24.

  2011

  Damien C. Croteau-Chonka; Amanda F. Marvelle; Ethan M. Lange; Nanette R. Lee; Linda S. Adair; Leslie A. Lange; Karen L. Mohlke

  Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in filipino women

  Obesity. 2011;19(5):1019-1027.
  12

• 25.

  2011

  Tuomas O. Kilpeläinen; Marcel Den Hoed; Ken K. Ong; Anders Grøntved; Soren Brage; Karen Jameson; Cyrus Cooper; Kay-Tee Khaw; Ulf Ekelund; Nicholas J. Wareham; et al.

  Obesity-susceptibility loci have a limited influence on birth weight: A meta-analysis of up to 28,219 individuals

  American Journal of Clinical Nutrition. 2011;93(4):851-860.
  12

• 26.

  2011

  Nicole Soranzo; Serena Sanna; Eleanor Wheeler; Christian Gieger; Dörte Radke; Josée Dupuis; Nabila Bouatia-Naji; Claudia Langenberg; Inga Prokopenko; Elliot Stolerman; et al.

  Common variants at 10 genomic loci influence hemoglobin A _1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))

  Diabetes. 2011;60(3):1051.
  0

• 27.

  2011

  Benjamin F. Voight; Laura J. Scott; Valgerdur Steinthorsdottir; Andrew P. Morris; Christian Dina; Ryan P Welch; Eleftheria Zeggini; Cornelia Huth; Yurii S. Aulchenko; Gudmar Thorleifsson; et al.

  Erratum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

  Nature Genetics. 2011;43(4):388.
  2

• 28.

  2010

  Nicole Soranzo; Serena Sanna; Eleanor Wheeler; Christian Gieger; Dörte Radke; Josée Dupuis; Nabila Bouatia-Naji; Claudia Langenberg; Inga Prokopenko; Elliot Stolerman; et al.

  Common variants at 10 genomic loci influence hemoglobin A_1C levels via glycemic and nonglycemic pathways

  Diabetes. 2010;59(12):3229-3239.
  58

• 29.

  2010

  Ying Wu; Yun Li; Ethan M. Lange; Damien C. Croteau-Chonka; Christopher W. Kuzawa; Thomas W. McDade; Li Qin; Ghenadie Curocichin; Judith B. Borja; Leslie A. Lange; et al.

  Genome-wide association study for adiponectin levels in filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ

  Human Molecular Genetics. 2010;19(24):4955-4964.
  16

• 30.

  2010

  Elizabeth K. Speliotes; Cristen J. Willer; Sonja I. Berndt; Keri L. Monda; Gudmar Thorleifsson; Anne U. Jackson; Hana Lango Allen; Cecilia M. Lindgren; Jian'An Luan; Reedik Mägi; et al.

  Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

  Nature Genetics. 2010;42(11):937-948.
  424

• 31.

  2010

  Iris M. Heid; Anne U Jackson; Joshua C. Randall; Tthomas W. Winkler; Llu Qi; Valgerdur Ssteinthorsdottir; Ggudmar Tthorleifsson; Ccarola Zillikens; Eelizabeth K. Sspeliotes; Reedik Mägi; 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. 2010;42(11):949-960.
  151

• 32.

  2010

  Dawn M. Waterworth; Sally L. Ricketts; Kijoung Song; Li Chen; Jing Hua Zhao; Samuli Ripatti; Yurii S. Aulchenko; Weihua Zhang; Xin Yuan; Noha Lim; et al.

  Genetic variants influencing circulating lipid levels and risk of coronary artery disease

  Arteriosclerosis, Thrombosis, and Vascular Biology. 2010;30(11):2264-2276.
  79

• 33.

  2010

  Hana Lango Allen; Karol Estrada; Guillaume Lettre; Sonja I. Berndt; Michael N. Weedon; Fernando Rivadeneira; Cristen J. Willer; Anne U. Jackson; Sailaja Vedantam; Soumya Raychaudhuri; et al.

  Hundreds of variants clustered in genomic loci and biological pathways affect human height

  Nature. 2010;467(7317):832-838.
  350

• 34.

  2010

  Randal J. Westrick; Karen L. Mohlke; Lindsey M. Korepta; Angela Y. Yang; Goujing Zhu; Sara L. Manning; Mary E. Winn; Kristiann M. Dougherty; David Ginsburg

  Spontaneous Irs1 passenger mutation linked to a gene-targeted SerpinB2 allele

  Proceedings of the National Academy of Sciences of the United States of America. 2010;107(39):16904-16909.
  2

• 35.

  2010

  Tanya M. Teslovich; Kiran Musunuru; Albert V. Smith; Andrew C. Edmondson; Ioannis M. Stylianou; Masahiro Koseki; James P. Pirruccello; Samuli Ripatti; Daniel I. Chasman; Cristen J. Willer; et al.

  Biological, clinical and population relevance of 95 loci for blood lipids

  Nature. 2010;466(7307):707-713.
  558

• 36.

  2010

  Benjamin F. Voight; Laura J. Scott; Valgerdur Steinthorsdottir; Andrew P. Morris; Christian Dina; Ryan P. Welch; Eleftheria Zeggini; Cornelia Huth; Yurii S. Aulchenko; Gudmar Thorleifsson; et al.

  Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

  Nature Genetics. 2010;42(7):579-589.
  418

• 37.

  2010

  Helena Furberg; Yunjung Kim; Jennifer Dackor; Eric Boerwinkle; Nora Franceschini; Diego Ardissino; Luisa Bernardinelli; Pier M. Mannucci; Francesco Mauri; Piera A. Merlini; et al.

  Genome-wide meta-analyses identify multiple loci associated with smoking behavior

  Nature Genetics. 2010;42(5):441-447.
  149

• 38.

  2010

  Josée Dupuis; Claudia Langenberg; Inga Prokopenko; Richa Saxena; Nicole Soranzo; Anne U. Jackson; Eleanor Wheeler; Nicole L. Glazer; Nabila Bouatia-Naji; Anna L. Gloyn; et al.

  Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116))

  Nature Genetics. 2010;42(5):464.
  1

• 39.

  2010

  Rachel M. Freathy; Dennis O. Mook-Kanamori; Ulla Sovio; Inga Prokopenko; Nicholas J. Timpson; Diane J Berry; Nicole M. Warrington; Elisabeth Widen; Jouke Jan Hottenga; Marika Kaakinen; et al.

  Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

  Nature Genetics. 2010;42(5):430-435.
  60

• 40.

  2010

  Erik Ingelsson; Claudia Langenberg; Marie-France Hivert; Inga Prokopenko; Valeriya Lyssenko; Josée Dupuis; Reedik Mägi; Stephen Sharp; Anne U. Jackson; Themistocles L. Assimes; et al.

  Detailed physiologic characterization reveals diverse mechanisms for novel genetic loci regulating glucose and insulin metabolism in humans

  Diabetes. 2010;59(5):1266-1275.
  71

• 41.

  2010

  Kyle J. Gaulton; Takao Nammo; Lorenzo Pasquali; Jeremy M. Simon; Paul G. Giresi; Marie P. Fogarty; Tami M. Panhuis; Piotr Mieczkowski; Antonio Secchi; Domenico Bosco; et al.

  A map of open chromatin in human pancreatic islets

  Nature Genetics. 2010;42(3):255-259.
  127

• 42.

  2010

  Marie P. Fogarty; Rui Xiao; Ludmila Prokunina-Olsson; Laura J. Scott; Karen L. Mohlke

  Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK

  Human Molecular Genetics. 2010;19(10):1921-1929.
  9

• 43.

  2010

  Leslie A. Lange; Damien C. Croteau-Chonka; Amanda F. Marvelle; Li Qin; Kyle J. Gaulton; Christopher W. Kuzawa; Thomas W. McDade; Yunfei Wang; Yun Li; Shawn Levy; et al.

  Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults

  Human Molecular Genetics. 2010;19(10):2050-2058.
  10

• 44.

  2010

  Josée Dupuis; Claudia Langenberg; Inga Prokopenko; Richa Saxena; Nicole Soranzo; Anne U. Jackson; Eleanor Wheeler; Nicole L. Glazer; Nabila Bouatia-Naji; Anna L. Gloyn; et al.

  New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

  Nature Genetics. 2010;42(2):105-116.
  424

• 45.

  2010

  Richa Saxena; Marie-France Hivert; Claudia Langenberg; Toshiko Tanaka; James S. Pankow; Peter Vollenweider; Valeriya Lyssenko; Nabila Bouatia-Naji; Josée Dupuis; Anne U. Jackson; et al.

  Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

  Nature Genetics. 2010;42(2):142-148.
  146

• 46.

  2009

  Benjamin F. Voight; Laura J. Scott; Valgerdur Steinthorsdottir; Christian Dina; Eleftheria Zeggini; Cornelia Huth; Yurii S. Aulchenko; Ryan P. Welch; Gudmar Thorleifsson; Laura J. McCulloch; et al.

  Parental origin of sequence variants associated with complex diseases

  Nature. 2009;462(7275):868-874.
  147

• 47.

  2009

  Iris M. Heid; Cornelia Huth; Ruth J. F. Loos; Florian Kronenberg; Vera Adamkova; Sonia S. Anand; Kristin Ardlie; Heike Biebermann; Peter Bjerregaard; Heiner Boeing; et al.

  Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: Does heterogeneity of estimates relate to study design?

  PLoS Genetics. 2009;5(10).
  24

• 48.

  2009

  Christopher Newton-Cheh; Toby Johnson; Vesela Gateva; Martin D Tobin; Murielle Bochud; Lachlan Coin; Samer S Najjar; Jing Hua Zhao; Simon C Heath; Susana Eyheramendy; et al.

  Genome-wide association study identifies eight loci associated with blood pressure

  Nature Genetics. 2009;41(6):666-676.
  364

• 49.

  2009

  Cecilia M. Lindgren; Iris M. Heid; Joshua C. Randall; Claudia Lamina; Valgerdur Steinthorsdottir; Lu Qi; Elizabeth K. Speliotes; Gudmar Thorleifsson; Cristen J. Willer; Blanca M. Herrera; et al.

  Genome-wide association scan meta-analysis identifies three loci influencing adiposity and fat distribution

  PLoS Genetics. 2009;5(6).
  156

• 50.

  2009

  Yan Liu; Hanna K. Sanoff; Hyunsoon Cho; Christin E. Burd; Chad Torrice; Karen L. Mohlke; Joseph G. Ibrahim; Nancy E. Thomas; Norman E. Sharpless

  INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis

  PLoS ONE. 2009;4(4).
  82

• 51.

  2009

  L. Zinman; H.N. Liu; C. Sato; Y. Wakutani; A.F. Marvelle; D. Moreno; K.E. Morrison; K.L. Mohlke; J. Bilbao; J. Robertson; et al.

  A mechanism for low penetrance in an ALS family with a novel SOD1 deletion

  Neurology. 2009;72(13):1153-1159.
  8

• 52.

  2009

  Inga Prokopenko; Claudia Langenberg; Jose C. Florez; Richa Saxena; Nicole Soranzo; Gudmar Thorleifsson; Ruth J. F. Loos; Alisa K. Manning; Anne U. Jackson; Yurii Aulchenko; et al.

  Variants in MTNR1B influence fasting glucose levels

  Nature Genetics. 2009;41(1):77-81.
  240

• 53.

  2009

  Sekar Kathiresan; Cristen J. Willer; Gina M. Peloso; Serkalem Demissie; Kiran Musunuru; Eric E. Schadt; Lee Kaplan; Derrick Bennett; Yun Li; Toshiko Tanaka; et al.

  Common variants at 30 loci contribute to polygenic dyslipidemia

  Nature Genetics. 2009;41(1):56-65.
  442

• 54.

  2009

  Cristen J. Willer; Elizabeth K. Speliotes; Ruth J. F. Loos; Shengxu Li; Cecilia M. Lindgren; Iris M. Heid; Sonja I. Berndt; Amanda L. Elliott; Anne U. Jackson; Claudia Lamina; et al.

  Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

  Nature Genetics. 2009;41(1):25-34.
  562

• 55.

  2008

  Karen L. Mohlke

  Nonsynonymous variants and fatty liver disease

  Nature Genetics. 2008;40(12):1394-1395.
  1

• 56.

  2008

  Kyle J. Gaulton; Cristen J. Wilier; Yun Li; Laura J. Scott; Karen N. Conneely; Anne U. Jackson; William L. Duren; Peter S. Chines; Narisu Narisu; Lori L. Bonnycastle; et al.

  Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes

  Diabetes. 2008;57(11):3136-3144.
  33

• 57.

  2008

  Karen L. Mohlke; Michael Boehnke; Gonçalo R. Abecasis

  Metabolic and cardiovascular traits: An abundance of recently identified common genetic variants

  Human Molecular Genetics. 2008;17(R2):R102-R108.
  34

• 58.

  2008

  Wei-Min Chen; Michael R. Erdos; Anne U. Jackson; Richa Saxena; Serena Sanna; Kristi D. Silver; Nicholas J. Timpson; Torben Hansen; Marco Orrù; Maria Grazia Piras; et al.

  Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels

  Journal of Clinical Investigation. 2008;118(7):2620-2628.
  77

• 59.

  2008

  Amanda F. Marvelle; Leslie A. Lange; Li Qin; Linda S. Adair; Karen L. Mohlke

  Association of FTO with Obesity-Related traits in the cebu longitudinal health and nutrition survey (CLHNS) cohort

  Diabetes. 2008;57(7):1987-1991.
  32

• 60.

  2008

  Ruth J. F. Loos; Cecilia M. Lindgren; Shengxu Li; Eleanor Wheeler; Jing Hua Zhao; Inga Prokopenko; Michael Inouye; Rachel M. Freathy; Antony P. Attwood; Jacques S. Beckmann; et al.

  Common variants near MC4R are associated with fat mass, weight and risk of obesity

  Nature Genetics. 2008;40(6):768-775.
  467

• 61.

  2008

  Guillaume Lettre; Anne U. Jackson; Christian Gieger; Fredrick R. Schumacher; Sonja I. Berndt; Serena Sanna; Susana Eyheramendy; Benjamin F. Voight; Johannah L. Butler; Candace Guiducci; et al.

  Identification of ten loci associated with height highlights new biological pathways in human growth

  Nature Genetics. 2008;40(5):584-591.
  251

• 62.

  2008

  P.W. Franks; O. Rolandsson; S.L. Debenham; K.A. Fawcett; F. Payne; C. Dina; P. Froguel; K.L. Mohlke; C. Willer; et al.

  Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations (Diabetologia DOI: 10.1007/s00125-007-0887-6)

  Diabetologia. 2008;51(3):523.
  1

• 63.

  2008

  P.W. Franks; O. Rolandsson; S.L. Debenham; K.A. Fawcett; F. Payne; C. Dina; P. Froguel; K.L. Mohlke; C. Willer; et al.

  Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

  Diabetologia. 2008;51(3):458-463.
  50

• 64.

  2008

  Serena Sanna; Anne U. Jackson; Ramaiah Nagaraja; Cristen J. Willer; Wei-Min Chen; Lori L. Bonnycastle; Haiqing Shen; Nicholas Timpson; Guillaume Lettre; Gianluca Usala; et al.

  Common variants in the GDF5-UQCC region are associated with variation in human height

  Nature Genetics. 2008;40(2):198-203.
  163

• 65.

  2008

  Cristen J. Willer; Serena Sanna; Anne U. Jackson; Angelo Scuteri; Lori L. Bonnycastle; Robert Clarke; Simon C. Heath; Nicholas J. Timpson; Samer S. Najjar; Heather M. Stringham; et al.

  Newly identified loci that influence lipid concentrations and risk of coronary artery disease

  Nature Genetics. 2008;40(2):161-169.
  587

• 66.

  2008

  Daniel Pomp; Karen L. Mohlke

  Obesity genes: So close and yet so far...

  Journal of Biology. 2008;7(9).
  6

• 67.

  2007

  Amanda F. Marvelle; Leslie A. Lange; Li Qin; Yunfei Wang; Ethan M. Lange; Linda S. Adair; Karen L. Mohlke

  Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples

  Journal of Human Genetics. 2007;52(9):729-737.
  10

• 68.

  2007

  Laura J. Scott; Karen L. Mohlke; Lori L. Bonnycastle; Cristen J. Willer; Yun Li; William L. Duren; Michael R. Erdos; Heather M. Stringham; Peter S. Chines; Anne U. Jackson; et al.

  A genome-wide association study of type 2 diabetes in finns detects multiple susceptibility variants

  Science. 2007;316(5829):1341-1345.
  1135

• 69.

  2007

  Kyle J. Gaulton; Karen L. Mohlke; Todd J. Vision

  A computational system to select candidate genes for complex human traits

  Bioinformatics. 2007;23(9):1132-1140.
  52

• 70.

  2007

  Cristen J. Willer; Lori L. Bonnycastle; Karen N. Conneely; William L. Duren; Anne U. Jackson; Laura J. Scott; Narisu Narisu; Peter S. Chines; Andrew Skol; et al.

  Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes

  Diabetes. 2007;56(1):256-264.
  43

• 71.

  2006

  Laura J. Scott; Lori L. Bonnycastle; Cristen J. Willer; Andrew G. Sprau; Anne U. Jackson; Narisu Narisu; William L. Duren; Peter S. Chines; Heather M. Stringham; et al.

  Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a finnish sample

  Diabetes. 2006;55(9):2649-2653.
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  Lori L. Bonnycastle; Cristen J. Willer; Karen N. Conneely; Anne U. Jackson; Cecily P. Burrill; Richard M. Watanabe; Peter S. Chines; Narisu Narisu; Laura J. Scott; et al.

  Common variants in maturity-onset diabetes of the young genes contribute to risk of type 2 diabetes in Finns

  Diabetes. 2006;55(9):2534-2540.
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  Cristen J. Willer; Laura J. Scott; Lori L. Bonnycastle; Anne U. Jackson; Peter Chines; Randall Pruim; Craig W. Bark; Ya-Yu Tsai; Elizabeth W. Pugh; et al.

  Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database

  Genetic Epidemiology. 2006;30(2):180-190.
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  Karen L. Mohlke; Anne U. Jackson; Laura J. Scott; Erin C. Peck; Yong D. Suh; Peter S. Chines; Richard M. Watanabe; Thomas A. Buchanan; Karen N. Conneely; et al.

  Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns

  Human Genetics. 2005;118(2):245-254.
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  2005

  Karen L. Mohlke; Andrew D. Skol; Laura J. Scott; Timo T. Valle; Richard N. Bergman; Jaakko Tuomilehto; Michael Boehnke; Francis S. Collins

  Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns

  Molecular Genetics and Metabolism. 2005;85(4):323-327.
  12

• 76.

  2005

  Karen L. Mohlke; Michael Boehnke

  The role of HNF4A variants in the risk of type 2 diabetes

  Current Diabetes Reports. 2005;5(2):149-156.
  13

• 77.

  2004

  K.N. Conneely; K. Silander; L.J. Scott; K.L. Mohlke; K.N. Lazaridis; T.T. Valle; J. Tuomilehto; R.N. Bergman; R.M. Watanabe; T.A. Buchanan; et al.

  Variation in the resistin gene is associated with obesity and insulin-related phenotypes in Finnish subjects

  Diabetologia. 2004;47(10):1782-1788.
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  2004

  Kaisa Silander; Karen L. Mohlke; Laura J. Scott; Erin C. Peck; Pablo Hollstein; Andrew D. Skol; Anne U. Jackson; Panagiotis Delonkas; Sarah Hunt; et al.

  Genetic Variation Near the Hepatocyte Nuclear Factor-4α Gene Predicts Susceptibility to Type 2 Diabetes

  Diabetes. 2004;53(4):1141-1149.
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  Kaisa Silander; Laura J. Scott; Timo T. Valle; Karen L. Mohlke; Heather M. Stringham; Kerry R. Wiles; William L. Duren; Kimberly F. Doheny; Elizabeth W. Pugh; Peter Chines; et al.

  A Large Set of Finnish Affected Sibling Pair Families with Type 2 Diabetes Suggests Susceptibility Loci on Chromosomes 6, 11, and 14

  Diabetes. 2004;53(3):821-829.
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  2002

  Karen L. Mohlke; Michael R. Erdos; Laura J. Scott; Tasha E. Fingerlin; Anne U. Jackson; Kaisa Silander; Pablo Hollstein; Michael Boehnke; Francis S. Collins

  High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools

  Proceedings of the National Academy of Sciences of the United States of America. 2002;99(26):16928-16933.
  75

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  2002

  Tasha E. Fingerlin; Michael R. Erdos; Richard M. Watanabe; Kerry R. Wiles; Heather M. Stringham; Karen L. Mohlke; Kaisa Silander; Timo T. Valle; Thomas A. Buchanan; et al.

  Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort

  Diabetes. 2002;51(5):1644-1648.
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  2001

  Julie A. Douglas; Michael R. Erdos; Richard M. Watanabe; Andi Braun; Cristy L. Johnston; Paul Oeth; Karen L. Mohlke; Timo T. Valle; Christian Ehnholm; et al.

  The peroxisome poliferator - Activated receptor-γ2 Pro 12Ala variant: Association with type 2 diabetes and trait differences

  Diabetes. 2001;50(4):886-890.
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  2001

  Karen L. Mohlke; Ethan M. Lange; Timo T. Valle; Soumitra Ghosh; Victoria L. Magnuson; Kaisa Silander; Richard M. Watanabe; Peter S. Chines; Richard N. Bergman; Jaakko Tuomilehto; et al.

  Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns

  Genome Research. 2001;11(7):1221-1226.
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  R.M. Watanabe; S. Ghosh; C.D. Langefeld; T.T. Valle; E.R. Hauser; V.L. Magnuson; K.L. Mohlke; K. Silander; D.S. Ally; P. Chines; et al.

  The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci

  American Journal of Human Genetics. 2000;67(5):1186-1200.
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  S. Ghosh; R.M. Watanabe; T.T. Valle; E.R. Hauser; V.L. Magnuson; C.D. Langefeld; D.S. Ally; K.L. Mohlke; K. Silander; K. Kohtamaki; et al.

  The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes

  American Journal of Human Genetics. 2000;67(5):1174-1185.
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  1999

  K.L. Mohlke; W.C. Nichols; D. Ginsburg

  The molecular basis of von Willebrand disease

  International Journal of Clinical and Laboratory Research. 1999;29(1):1-7.
  9

• 87.

  1999

  Karen L. Mohlke; Anjali A. Purkayastha; Randal J. Westrick; Peter L. Smith; Bronia Petryniak; John B. Lowe; David Ginsburg

  Mvwf, a dominant modifier of murine von Willebrand factor, results from altered lineage-specific expression of a glycosyltransferase

  Cell. 1999;96(1):111-120.
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  K.L. Mohlke; W.C. Nichols; D. Ginsburg

  The molecular basis of von Willebrand disease

  Clinical and Experimental Medicine. 1999;29(1):1-7.
  0

• 89.

  1998

  Karen L. Mohlke; Anjali A. Purkayastha; Randal J. Westrick; David Ginsburg

  Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a Region containing a modifying locus for murine plasma von Willebrand factor level

  Genomics. 1998;54(1):19-30.
  8

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  1997

  Karen L. Mohlke; David Ginsburg

  Von Willebrand disease and quantitative variation in von Willebrand factor

  Journal of Laboratory and Clinical Medicine. 1997;130(3):252-261.
  32

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  1996

  Karen L. Mohlke; William C. Nichols; Randal J. Westrick; Edward K. Novak; Kathleen A. Cooney; Richard T. Swank; David Ginsburg

  A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11

  Proceedings of the National Academy of Sciences of the United States of America. 1996;93(26):15352-15357.
  46

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  1996

  Karen L. Mohlke; William C. Nichols; Alnawaz Rehemtulla; Randal J. Kaufman; Heidi M. Fagerström; K.L. Annukka Ritvanen; Riitta Kekomäki; David Ginsburg

  A common frameshift mutation in von Willebrand factor does not alter mRNA stability but interferes with normal propeptide processing

  British Journal of Haematology. 1996;95(1):184-191.
  16

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  1995

  W.C. Nichols; K.A. Cooney; K.L. Mohlke; J.D. Ballew; A. Yang; M.E. Bruck; M. Reddington; E.K. Novak; R.T. Swank; et al.

  von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene.

  Blood. 1995;86(6):2461.
  1

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  1994

  William C. Nichols; Kathleen A. Cooney; Karen L. Mohlke; Jeffrey D. Ballew; Angela Yang; Mary E. Bruck; Madonna Reddington; Edward K. Novak; Richard T. Swank; et al.

  von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene

  Blood. 1994;83(11):3225-3231.
  51

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  1993

  Lon L. Barrow; Karl Simin; Karen Mohlke; William C. Nichols; David Ginsburg; Miriam H. Meisler

  Conserved linkage of neurotrophin-3 and von Willebrand factor on mouse Chromosome 6

  Mammalian Genome. 1993;4(6):343-345.
  8