M
Michael Boehnke
Researcher at University of Michigan
Publications - 540
Citations - 155551
Michael Boehnke is an academic researcher from University of Michigan. The author has contributed to research in topics: Genome-wide association study & Type 2 diabetes. The author has an hindex of 152, co-authored 511 publications receiving 136681 citations. Previous affiliations of Michael Boehnke include SUNY Downstate Medical Center & Norwegian University of Science and Technology.
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Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in
Finns 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,Sareena T. Enloe,Amy J. Swift,William L. Duren,Heather M. Stringham,Michael R. Erdos,Nancy Riebow,Thomas A. Buchanan,Timo T. Valle,Jaakko Tuomilehto,Richard N. Bergman,Karen L. Mohlke,Michael Boehnke,Francis S. Collins +21 more
TL;DR: Evidence is found of type 2 diabetes association with SNPs in five of the six known MODY genes: GCK, H NF1A, HNF1B, NEUROD1, and HNF4A, which suggests that common variants in several MODy genes play a modest role in type 2abetes susceptibility.
Posted ContentDOI
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation
Natasha H. J. Ng,Natasha H. J. Ng,Sara M. Willems,Juan P. Fernandez,Rebecca S. Fine,Rebecca S. Fine,Rebecca S. Fine,Eleanor Wheeler,Eleanor Wheeler,Jennifer Wessel,Hidetoshi Kitajima,Gaëlle Marenne,Jana K. Rundle,Xueling Sim,Xueling Sim,Hanieh Yeghootkar,Nicola L. Beer,Anne Raimondo,A. I. Tarasov,Soren K. Thomsen,Soren K. Thomsen,Martijn van de Bunt,Shuai Wang,Sai Chen,Yuning Chen,Yii-Der Ida Chen,Hugoline G. de Haan,Niels Grarup,Ruifang Li-Gao,Tibor V. Varga,Jennifer L. Asimit,Jennifer L. Asimit,Shuang Feng,Rona J. Strawbridge,Rona J. Strawbridge,Erica L. Kleinbrink,Tarunveer S. Ahluwalia,Tarunveer S. Ahluwalia,Ping An,Emil V. R. Appel,Dan E. Arking,Juha Auvinen,Juha Auvinen,Lawrence F. Bielak,Nathan A. Bihlmeyer,Jette Bork-Jensen,Jennifer A. Brody,Archie Campbell,Audrey Y. Chu,Gail Davies,Ayse Demirkan,James S. Floyd,Franco Giulianini,Xiuqing Guo,Stefan Gustafsson,Benoit Hastoy,Anne U. Jackson,Johanna Jakobsdottir,Marjo-Riitta Järvelin,Marjo-Riitta Järvelin,Richard A. Jensen,Stavroula Kanoni,Sirkka Keinänen-Kiukaanniemi,Sirkka Keinänen-Kiukaanniemi,Jin Li,Man Li,Man Li,Kurt Lohman,Yingchang Lu,Yingchang Lu,Jian'an Luan,Alisa K. Manning,Jonathan Marten,Carola Marzi,Karina Meidtner,Dennis O. Mook-Kanamori,Taulant Muka,Taulant Muka,Giorgio Pistis,Giorgio Pistis,Bram P. Prins,Kenneth Rice,Neil Robertson,Serena Sanna,Serena Sanna,Yuan Shi,Albert V. Smith,Jennifer A. Smith,Lorraine Southam,Lorraine Southam,Heather M. Stringham,Salman M. Tajuddin,Vinicius Tragante,Sander W. van der Laan,Helen R. Warren,Jie Yao,Andrianos M. Yiorkas,Andrianos M. Yiorkas,Weihua Zhang,Weihua Zhang,Wei Zhao,Emma Ahlqvist,Mariaelisa Graff,Heather M. Highland,Heather M. Highland,Anne E. Justice,Ken Sin Lo,Eirini Marouli,Carolina Medina-Gomez,Saima Afaq,Wesam A Alhejily,Wesam A Alhejily,Najaf Amin,Folkert W. Asselbergs,Folkert W. Asselbergs,Lori L. Bonnycastle,Michiel L. Bots,Ivan Brandslund,Ji Chen,Cramer Christensen,John Danesh,Renée de Mutsert,Abbas Dehghan,Abbas Dehghan,Tapani Ebeling,Paul Elliott,Aliki-Eleni Farmaki,Aliki-Eleni Farmaki,Jessica D. Faul,Paul W. Franks,Paul W. Franks,Paul W. Franks,Steve Franks,Andreas Fritsche,Anette P. Gjesing,Mark O. Goodarzi,Vilmundur Gudnason,Göran Hallmans,Tamara B. Harris,Karl-Heinz Herzig,Karl-Heinz Herzig,Marie-France Hivert,Jan-Håkan Jansson,Min A. Jhun,Min A. Jhun,Torben Jørgensen,Torben Jørgensen,Torben Jørgensen,Marit E. Jørgensen,Marit E. Jørgensen,Pekka Jousilahti,Eero Kajantie,Maria Karaleftheri,Sharon L.R. Kardia,Leena Kinnunen,Heikki A. Koistinen,Heikki A. Koistinen,Heikki A. Koistinen,Pirjo Komulainen,Peter Kovacs,Johanna Kuusisto,Markku Laakso,Leslie A. Lange,Lenore J. Launer,Jung-Jin Lee,Aaron Leong,Jaana Lindström,Jocelyn E. Manning Fox,Satu Männistö,Nisa M. Maruthur,Nisa M. Maruthur,Leena Moilanen,Antonella Mulas,Antonella Mulas,Mike A. Nalls,Matt J. Neville,James S. Pankow,Alison Pattie,Eva Rabing Brix Petersen,Hannu Puolijoki,Asif Rasheed,Paul Redmond,Frida Renström,Frida Renström,Michael Roden,Danish Saleheen,Juha Saltevo,Kai Savonen,Sylvain Sebert,Tea Skaaby,Kerrin S. Small,Alena Stančáková,Jakob Stokholm,Konstantin Strauch,E-Shyong Tai,Kent D. Taylor,Betina H. Thuesen,Anke Tönjes,Emmanouil Tsafantakis,Tiinamaija Tuomi,Tiinamaija Tuomi,Jaakko Tuomilehto,Matti Uusitupa,Marja Vääräsmäki,Marja Vääräsmäki,Ilonca Vaartjes,Magdalena Zoledziewska,Gonçalo R. Abecasis,Beverley Balkau,Hans Bisgaard,Alexandra I. F. Blakemore,Alexandra I. F. Blakemore,Matthias Blüher,Heiner Boeing,Eric Boerwinkle,Klaus Bønnelykke,Erwin P. Bottinger,Mark J. Caulfield,John C. Chambers,John C. Chambers,John C. Chambers,Daniel I. Chasman,Daniel I. Chasman,Ching-Yu Cheng,Anne Clark,Francis S. Collins,Josef Coresh,Francesco Cucca,Francesco Cucca,Gert J. de Borst,Ian J. Deary,George Dedoussis,Panos Deloukas,Panos Deloukas,Hester M. den Ruijter,Josée Dupuis,Josée Dupuis,Michele K. Evans,Ele Ferrannini,Oscar H. Franco,Oscar H. Franco,Harald Grallert,Leif Groop,Leif Groop,Torben Hansen,Torben Hansen,Andrew T. Hattersley,Caroline Hayward,Joel N. Hirschhorn,Joel N. Hirschhorn,Joel N. Hirschhorn,Arfan Ikram,Erik Ingelsson,Fredrik Karpe,Fredrik Karpe,Kay-Tee Kaw,Wieland Kiess,Jaspal S. Kooner,Jaspal S. Kooner,Jaspal S. Kooner,Antje Körner,Timo A. Lakka,Claudia Langenberg,Lars Lind,Cecilia M. Lindgren,Allan Linneberg,Allan Linneberg,Leonard Lipovich,Ching-Ti Liu,Jun Liu,Yongmei Liu,Ruth J. F. Loos,Patrick E. MacDonald,Karen L. Mohlke,Andrew D. Morris,Patricia B. Munroe,Alison D. Murray,Sandosh Padmanabhan,Colin N. A. Palmer,Gerard Pasterkamp,Oluf Pedersen,Patricia A. Peyser,Ozren Polasek,David J. Porteous,Michael A. Province,Bruce M. Psaty,Rainer Rauramaa,Paul M. Ridker,Paul M. Ridker,Olov Rolandsson,Patrik Rorsman,Patrik Rorsman,Frits R. Rosendaal,Igor Rudan,Veikko Salomaa,Matthias B. Schulze,Robert Sladek,Blair H. Smith,Tim D. Spector,John M. Starr,Michael Stumvoll,Cornelia M. van Duijn,Mark Walker,Nicholas J. Wareham,David R. Weir,James G. Wilson,Tien Yin Wong,Eleftheria Zeggini,Alan B. Zonderman,Jerome I. Rotter,Andrew P. Morris,Andrew P. Morris,Michael Boehnke,Jose C. Florez,Mark I. McCarthy,Mark I. McCarthy,James B. Meigs,James B. Meigs,Anubha Mahajan,Robert A. Scott,Anna L. Gloyn,Anna L. Gloyn,Inês Barroso,Inês Barroso +323 more
TL;DR: In this paper, the authors investigated associations of exome-array variants in up to 144,060 individuals without diabetes of multiple ancestries, and found that a novel FG/FI association at the liver-enriched G6PC transcript was driven by multiple rare loss-of-function variants.
Journal ArticleDOI
Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traits.
Sarah M Brotman,Chelsea K. Raulerson,Swarooparani Vadlamudi,Kevin W Currin,Qiujin Shen,Victoria A. Parsons,Apoorva K Iyengar,Tamara S. Roman,Terrence S. Furey,Johanna Kuusisto,Francis S. Collins,Michael Boehnke,Markku Laakso,Päivi Pajukanta,Karen L. Mohlke +14 more
TL;DR: The authors used subcutaneous adipose tissue of 426 Finnish men from the METSIM study and identified splice junction quantitative trait loci (sQTLs) for 6,077 splice junctions (FDR < 1%).
Journal ArticleDOI
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
Liron Ganel,Lei Chen,Ryan Christ,Jagadish Vangipurapu,Erica Young,Indraniel Das,Krishna L. Kanchi,David E. Larson,Allison A. Regier,Haley J. Abel,Chul Joo Kang,Alexandra J. Scott,Aki S. Havulinna,Aki S. Havulinna,Charleston W. K. Chiang,Nelson B. Freimer,Aarno Palotie,Aarno Palotie,Aarno Palotie,Samuli Ripatti,Samuli Ripatti,Johanna Kuusisto,Michael Boehnke,Markku Laakso,Adam E. Locke,Nathan O. Stitziel,Ira M. Hall,Ira M. Hall +27 more
TL;DR: In this paper, the authors used a Mendelian randomization framework to identify two loci significantly associated with mt-CN variation: a common variant at the MYB-HBS1L locus and a burden of rare variants in the TMBIM1 gene.
Journal ArticleDOI
An Algorithm to Construct Genetically Similar Subsets of Families with the Use of Self-Reported Ethnicity Information
TL;DR: A simple algorithm that uses self-reported ethnicity information, pedigree structure, and affection status to group families into genetically more homogeneous subsets to prove useful to researchers who wish to perform genetic analyses on more-homogeneous subset when they suspect that ignoring heterogeneity could lead to false-positive results or loss of power.