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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Journal ArticleDOI
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
Robert A. Scott,Daniel F. Freitag,Daniel F. Freitag,Li Li,Audrey Y. Chu,Praveen Surendran,Robin Young,Niels Grarup,Alena Stančáková,Yuning Chen,Tibor V. Varga,Hanieh Yaghootkar,Jian'an Luan,Jing Hua Zhao,Sara M. Willems,Sara M. Willems,Jennifer Wessel,Shuai Wang,Nisa M. Maruthur,Nisa M. Maruthur,Kyriaki Michailidou,Ailith Pirie,Sven J. van der Lee,Christopher J. Gillson,Ali Amin Al Olama,Philippe Amouyel,Larraitz Arriola,Dominique Arveiler,Iciar Aviles-Olmos,Beverley Balkau,Aurelio Barricarte,Inês Barroso,Inês Barroso,Sara Benlloch Garcia,Joshua C. Bis,Stefan Blankenberg,Michael Boehnke,Heiner Boeing,Eric Boerwinkle,Eric Boerwinkle,Ingrid B. Borecki,Jette Bork-Jensen,Sarah Bowden,Carlos Caldas,Muriel J. Caslake,L. Adrienne Cupples,L. Adrienne Cupples,Carlos Cruchaga,Jacek Czajkowski,Marcel den Hoed,Janet A. Dunn,Helena M. Earl,Georg Ehret,Ele Ferrannini,Jean Ferrières,Thomas Foltynie,Ian Ford,Nita G. Forouhi,Francesco Gianfagna,Carlos González,Sara Grioni,Louise Hiller,Jan-Håkan Jansson,Marit E. Jørgensen,Marit E. Jørgensen,J. Wouter Jukema,Rudolf Kaaks,Frank Kee,Nicola D. Kerrison,Timothy J. Key,Jukka Kontto,Zsofia Kote-Jarai,Aldi T. Kraja,Kari Kuulasmaa,Johanna Kuusisto,Allan Linneberg,Chunyu Liu,Gaëlle Marenne,Karen L. Mohlke,Andrew P. Morris,Andrew P. Morris,Kenneth Muir,Kenneth Muir,Martina Müller-Nurasyid,Patricia B. Munroe,Carmen Navarro,Sune F. Nielsen,Peter M. Nilsson,Børge G. Nordestgaard,Chris J. Packard,Domenico Palli,Salvatore Panico,Gina M. Peloso,Gina M. Peloso,Markus Perola,Markus Perola,Annette Peters,Christopher J. Poole,Christopher J. Poole,J. Ramón Quirós,Olov Rolandsson,Carlotta Sacerdote,Veikko Salomaa,María José Sánchez,Naveed Sattar,Stephen J. Sharp,Rebecca Sims,Nadia Slimani,Jennifer A. Smith,Deborah J. Thompson,Stella Trompet,Rosario Tumino,Daphne L. van der A,Yvonne T. van der Schouw,Jarmo Virtamo,Mark Walker,Klaudia Walter,EPIC-InterAct,Jean Abraham,Laufey T. Amundadottir,Jennifer L. Aponte,Adam S. Butterworth,Josée Dupuis,Douglas F. Easton,Douglas F. Easton,Rosalind A. Eeles,Jeanette Erdmann,Jeanette Erdmann,Jeanette Erdmann,Paul W. Franks,Timothy M. Frayling,Torben Hansen,Joanna M. M. Howson,Joanna M. M. Howson,Torben Jørgensen,Torben Jørgensen,Torben Jørgensen,Jaspal S. Kooner,Markku Laakso,Claudia Langenberg,Claudia Langenberg,Mark I. McCarthy,James S. Pankow,Oluf Pedersen,Elio Riboli,Jerome I. Rotter,Danish Saleheen,Danish Saleheen,Nilesh J. Samani,Heribert Schunkert,Peter Vollenweider,Peter Vollenweider,Stephen O'Rahilly,Panos Deloukas,Panos Deloukas,John Danesh,Mark O. Goodarzi,Mark O. Goodarzi,Sekar Kathiresan,James B. Meigs,Margaret G. Ehm,Nicholas J. Wareham,Dawn M. Waterworth +162 more
TL;DR: A low-frequency missense variant in the gene encoding glucagon-like peptide-1 receptor, the target of GLP1R agonists, was associated with lower fasting glucose and T2D risk, consistent with GLP 1R agonist therapies, and provided evidence that GLP2D agonists are not likely to be associated with an unacceptable increase in cardiovascular risk.
Journal ArticleDOI
Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation
Lori L. Bonnycastle,Peter S. Chines,Takashi Hara,Jeroen R. Huyghe,Amy J. Swift,Pirkko Heikinheimo,Jana Mahadevan,Sirkku Peltonen,Hanna Huopio,Pirjo Nuutila,Pirjo Nuutila,Narisu Narisu,Rachel L. Goldfeder,Michael L. Stitzel,Simin Lu,Michael Boehnke,Fumihiko Urano,Francis S. Collins,Markku Laakso +18 more
TL;DR: A novel nonsynonymous variant (p.Trp314Arg) in the Wolfram syndrome 1 (WFS1) gene is uncovered that segregates completely with the diabetic phenotype and represents the first compelling report of a mutation in WFS1 associated with dominantly inherited nonsyndromic adult-onset diabetes.
Defining the role of common variation in the genomic and biological architecture of adult human height
Andrew R. Wood,Tõnu Esko,Jian Yang,Sailaja Vedantam,Tune H. Pers,Stefan Gustafsson,Audrey Y. Chun,Karol Estrada,Jian'an Luan,Zoltán Kutalik,Najaf Amin,Martin L. Buchkovich,Damien C. Croteau-Chonka,Felix R. Day,Yanan Duan,Tove Fall,Rudolf S N Fehrmann,Teresa Ferreira,Anne U. Jackson,Juha Karjalainen,Ken Sin Lo,Adam E. Locke,Reedik Maegi,Evelin Mihailov,Eleonora Porcu,Joshua C. Randall,André Scherag,Anna A. E. Vinkhuyzen,Harm-Jan Westra,Thomas W. Winkler,Tsegaselassie Workalemahu,Jing Hua Zhao,Devin Absher,Eva Albrecht,Denise Anderson,Jeffrey Baron,Marian Beekman,Ayse Demirkan,Georg Ehret,Bjarke Feenstra,Mary F. Feitosa,Krista Fischer,Ross M. Fraser,Anuj Goel,Jian Gong,Anne E. Justice,Stavroula Kanoni,Marcus E. Kleber,Kati Kristiansson,Unhee Lim,Vaneet Lotay,Julian C. Lui,Massimo Mangino,Irene Mateo Leach,Carolina Medina-Gomez,Mike A. Nalls,Dale R. Nyholt,Cameron D. Palmer,Dorota Pasko,Sonali Pechlivanis,Inga Prokopenko,Janina S. Ried,Stephan Ripke,Dmitry Shungin,Alena Stančáková,Rona J. Strawbridge,Yun Ju Sung,Toshiko Tanaka,Alexander Teumer,Stella Trompet,Sander W. van der Laan,Jessica van Setten,Jana V. van Vliet-Ostaptchouk,Zhaoming Wang,Loic Yengo,Weihua Zhang,Uzma Afzal,Johan Arnloev,Gillian M. Arscott,Stefania Bandinelli,Amy Barrett,Claire Bellis,Amanda J. Bennett,Christian Berne,Matthias Blueher,Jennifer L. Bolton,Yvonne Boettcher,Heather A. Boyd,Marcel Bruinenberg,Brendan M. Buckley,Steven Buyske,Ida Henriette Caspersen,Peter S. Chines,Robert Clarke,Simone Claudi-Boehm,Mark E. Cooper,E. Warwick Daw,Pim A. de Jong,Joris Deelen,Graciela E. Delgado,Josh C. Denny,Rosalie A. M. Dhonukshe-Rutten,Maria Dimitriou,Alex S. F. Doney,Marcus Doerr,Niina Eklund,Elodie Eury,Lasse Folkersen,Melissa E. Garcia,Frank Geller,Vilmantas Giedraitis,Alan S. Go,Harald Grallert,Tanja B. Grammer,Juergen Graessler,Henrik Groenberg,Lisette C. P. G. M. de Groot,Christopher J. Groves,Jeffrey Haessler,Per Hall,Toomas Haller,Göran Hallmans,Anke Hannemann,Catharina A. Hartman,Maija Hassinen,Caroline Hayward,Nancy L. Heard-Costa,Quinta Helmer,Gibran Hemani,Anjali K. Henders,Hans L. Hillege,Mark A. Hlatky,Wolfgang Hoffmann,Per Hoffmann,Oddgeir L. Holmen,Jeanine J. Houwing-Duistermaat,Thomas Illig,Aaron Isaacs,Alan L. James,Janina M. Jeff,Bent Johansen,Åsa Johansson,Jennifer Jolley,Thorhildur Juliusdottir,Juhani Junttila,Abel N. Kho,Leena Kinnunen,Norman Klopp,Thomas D. Kocher,Wolfgang Kratzer,Peter Lichtner,Lars Lind,Jaana Lindstroem,Stéphane Lobbens,Mattias Lorentzon,Yingchang Lu,Valeriya Lyssenko,Patrik K. E. Magnusson,Anubha Mahajan,Marc Maillard,Wendy L. McArdle,Colin A. McKenzie,Stela McLachlan,Paul J. McLaren,Cristina Menni,Sigrun Merger,Lili Milani,Alireza Moayyeri,Keri L. Monda,Mario A. Morken,Gabriele Mueller,Martina Mueller-Nurasyid,Arthur W. Musk,Narisu Narisu,Matthias Nauck,Ilja M. Nolte,Markus M. Noethen,Laticia Oozageer,Stefan Pilz,Nigel W. Rayner,Frida Renström,Neil R. Robertson,Lynda M. Rose,Ronan Roussel,Serena Sanna,Hubert Scharnagl,Salome Scholtens,Fredrick R. Schumacher,Heribert Schunkert,Robert A. Scott,Joban Sehmi,Thomas Seufferlein,Jianxin Shin,Karri Silventoinen,Johannes H. Smit,Albert V. Smith,Joanna Smolonska,Alice Stanton,Kathleen Stirrups,David J. Stott,Heather M. Stringham,Johan Sundström,Morris A. Swertz,Ann-Christine Syvänen,Bamidele O. Tayo,Gudmar Thorleifsson,Jonathan Tyrer,Suzanne C. van Dijk,Natasja M. van Schoor,Nathalie van der Velde,Diana van Heemst,Floor V. A. van Oort,Sita H. Vermeulen,Niek Verweij,Judith M. Vonk,Lindsay L. Waite,Melanie Waldenberger,Roman Wennauer,Lynne R. Wilkens,Christina Willenborg,Tom Wilsgaard,Mary K. Wojczynski,Andrew Wong,Alan F. Wright,Qunyuan Zhang,Dominique Arveiler,Stephan J. L. Bakker,John Beilby,Richard N. Bergman,Sven Bergmann,Reiner Biffar,John Blangero,Dorret I. Boomsma,Stefan R. Bornstein,Pascal Bovet,Paolo Brambilla,Morris J. Brown,Harry Campbell,Mark J. Caulfield,Aravinda Chakravarti,Rory Collins,Francis S. Collins,Dana C. Crawford,L. Adrienne Cupples,John Danesh,Ulf de Faire,Hester M. den Ruijter,Raimund Erbel,Jeanette Erdmann,Johan G. Eriksson,Martin Farrall,Ele Ferrannini,Jean Ferrières,Ian Ford,Nita G. Forouhi,Terrence Forrester,Ron T. Gansevoort,Pablo V. Gejman,Christian Gieger,Alain Golay,Omri Gottesman,Vilmundur Gudnason,Ulf Gyllensten,David W. Haas,Alistair S. Hall,Tamara B. Harris,Andrew T. Hattersley,Andrew C. Heath,Christian Hengstenberg,Andrew A. Hicks,Lucia A. Hindorff,Aroon D. Hingorani,Albert Hofman,G. Kees Hovingh,Steve E. Humphries,Steven C. Hunt,Elina Hyppönen,Kevin B. Jacobs,Marjo-Riitta Järvelin,Pekka Jousilahti,Antti Jula,Jaakko Kaprio,John J.P. Kastelein,Manfred Kayser,Frank Kee,Sirkka Keinänen-Kiukaanniemi,Lambertus A. Kiemeney,Jaspal S. Kooner,Charles Kooperberg,Seppo Koskinen,Peter Kovacs,Aldi T. Kraja,Meena Kumari,Johanna Kuusisto,Timo A. Lakka,Claudia Langenberg,Loic Le Marchand,Terho Lehtimäki,Sara Lupoli,Pamela A. F. Madden,Satu Männistö,Paolo Manunta,André Marette,Tara C. Matise,Barbara McKnight,Thomas Meitinger,Frans L. Moll,Grant W. Montgomery,Andrew D. Morris,Andrew P. Morris,Jeffrey C. Murray,Mari Nelis,Claes Ohlsson,Albertine J. Oldehinkel,Ken K. Ong,Willem H. Ouwehand,Gerard Pasterkamp,Annette Peters,Peter P. Pramstaller,Jackie F. Price,Lu Qi,Olli T. Raitakari,Tuomo Rankinen,Dabeeru C. Rao,Treva Rice,Marylyn D. Ritchie,Igor Rudan,Veikko Salomaa,Nilesh J. Samani,Jouko Saramies,Mark A. Sarzynski,Peter Schwarz,Sylvain Sebert,Peter S. Sever,Alan R. Shuldiner,Juha Sinisalo,Valgerdur Steinthorsdottir,Ronald P. Stolk,Jean-Claude Tardif,Anke Toenjes,Angelo Tremblay,Elena Tremoli,Jarmo Virtamo,Marie-Claude Vohl,Philippe Amouyel,Folkert W. Asselbergs,Themistocles L. Assimes,Murielle Bochud,Bernhard O. Boehm,Eric Boerwinkle,Erwin P. Bottinger,Claude Bouchard,Stéphane Cauchi,John C. Chambers,Stephen J. Chanock,Richard S. Cooper,Paul I.W. de Bakker,George Dedoussis,Luigi Ferrucci,Paul W. Franks,Philippe Froguel,Leif Groop,Christopher A. Haiman,Anders Hamsten,M. Geoffrey Hayes,Jennie Hui,David J. Hunter,Kristian Hveem,J. Wouter Jukema,Robert C. Kaplan,Mika Kivimäki,Diana Kuh,Markku Laakso,Yongmei Liu,Nicholas G. Martin,Winfried Maerz,Mads Melbye,Susanne Moebus,Patricia B. Munroe,Inger Njølstad,Ben A. Oostra,Colin N. A. Palmer,Nancy L. Pedersen,Markus Perola,Louis Pérusse,Ulrike Peters,Joseph E. Powell,Chris Power,Thomas Quertermous,Rainer Rauramaa,Eva Reinmaa,Paul M. Ridker,Fernando Rivadeneira,Jerome I. Rotter,Timo Saaristo,Danish Saleheen,David Schlessinger,P. Eline Slagboom,Harold Snieder,Tim D. Spector,Konstantin Strauch,Michael Stumvoll,Jaakko Tuomilehto,Matti Uusitupa,Pim van der Harst,Henry Voelzke,Mark Walker,Nicholas J. Wareham,Hugh Watkins,H-Erich Wichmann,James F. Wilson,Pieter Zanen,Panos Deloukas,Iris M. Heid,Cecilia M. Lindgren,Karen L. Mohlke,Elizabeth K. Speliotes,Unnur Thorsteinsdottir,Inês Barroso,Caroline S. Fox,Kari E. North,David P. Strachan,Jacques S. Beckmann,Sonja I. Berndt,Michael Boehnke,Ingrid B. Borecki,Mark I. McCarthy,Andres Metspalu,Kari Stefansson,André G. Uitterlinden,Cornelia M. van Duijn,Lude Franke,Cristen J. Willer,Alkes L. Price,Guillaume Lettre,Ruth J. F. Loos,Michael N. Weedon,Erik Ingelsson,Jeffrey R. O'Connell,Gonçalo R. Abecasis,Daniel I. Chasman,Michael E. Goddard,Peter M. Visscher,Joel N. Hirschhorn,Timothy M. Frayling +444 more
TL;DR: The results indicate a genetic architecture for human height that is characterized by a very large but finite number of causal variants, including mTOR, osteoglycin and binding of hyaluronic acid.
Journal ArticleDOI
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
Viktoria Gusarova,Colm O'Dushlaine,Tanya M. Teslovich,Peter N. Benotti,Tooraj Mirshahi,Omri Gottesman,Cristopher V. Van Hout,Michael F. Murray,Anubha Mahajan,Jonas B. Nielsen,Lars G. Fritsche,Anders Berg Wulff,Daniel F. Gudbjartsson,Marketa Sjögren,Connor A. Emdin,Robert A. Scott,Wen-Jane Lee,Aeron Small,Lydia Coulter Kwee,Om Prakash Dwivedi,Rashmi B. Prasad,Shannon Bruse,Alexander Lopez,John Penn,Anthony Marcketta,Joseph B. Leader,Christopher D. Still,H. Lester Kirchner,Uyenlinh L. Mirshahi,Amr H. Wardeh,Cassandra M. Hartle,Lukas Habegger,Samantha N. Fetterolf,Teresa Tusié-Luna,Andrew P. Morris,Andrew P. Morris,Andrew P. Morris,Hilma Holm,Valgerdur Steinthorsdottir,Patrick Sulem,Unnur Thorsteinsdottir,Jerome I. Rotter,Lee-Ming Chuang,Scott M. Damrauer,Scott M. Damrauer,David Birtwell,Chad M. Brummett,Amit Khera,Amit Khera,Pradeep Natarajan,Pradeep Natarajan,Marju Orho-Melander,Jason Flannick,Jason Flannick,Luca A. Lotta,Cristen J. Willer,Oddgeir L. Holmen,Marylyn D. Ritchie,David H. Ledbetter,Andrew J. Murphy,Ingrid B. Borecki,Jeffrey G. Reid,John D. Overton,Ola Hansson,Ola Hansson,Leif Groop,Leif Groop,Svati H. Shah,William E. Kraus,Daniel J. Rader,Yii-Der Ida Chen,Kristian Hveem,Kristian Hveem,Nicholas J. Wareham,Sekar Kathiresan,Olle Melander,Kari Stefansson,Børge G. Nordestgaard,Anne Tybjærg-Hansen,Gonçalo R. Abecasis,David Altshuler,Jose C. Florez,Jose C. Florez,Michael Boehnke,Mark I. McCarthy,Mark I. McCarthy,George D. Yancopoulos,David J. Carey,Alan R. Shuldiner,Aris Baras,Frederick E. Dewey,Jesper Gromada +91 more
TL;DR: It is found that predicted loss-of-function variants in ANGPTL4 are associated with glucose homeostasis and reduced risk of type 2 diabetes and that Angptl4−/− mice on a high-fat diet show improved insulin sensitivity.
Journal ArticleDOI
A genome-wide association study of IVGTT-based measures of first-phase insulin secretion refines the underlying physiology of type 2 diabetes variants
Andrew R. Wood,Anna Jonsson,Anne U. Jackson,Nan Wang,Nienke van Leewen,Nicholette D. Palmer,Sayuko Kobes,Joris Deelen,Lorena Boquete-Vilarino,Jussi Paananen,Alena Stančáková,Dorret I. Boomsma,Eco J. C. de Geus,Elisabeth M. W. Eekhoff,Andreas Fritsche,Mark H. H. Kramer,Giel Nijpels,Annemarie M. C. Simonis-Bik,Timon W. van Haeften,Anubha Mahajan,Michael Boehnke,Richard N. Bergman,Jaakko Tuomilehto,Francis S. Collins,Karen L. Mohlke,Karina Banasik,Karina Banasik,Christopher J. Groves,Mark I. McCarthy,Mark I. McCarthy,Mark I. McCarthy,Ewan R. Pearson,Andrea Natali,Andrea Mari,Thomas A. Buchanan,Kent D. Taylor,Kent D. Taylor,Anny H. Xiang,Anette P. Gjesing,Niels Grarup,Hans Eiberg,Oluf Pedersen,Yii-Derr Chen,Markku Laakso,Jill M. Norris,Ulf Smith,Lynne E. Wagenknecht,Leslie J. Baier,Donald W. Bowden,Torben Hansen,Mark Walker,Richard M. Watanabe,Leen M 't Hart,Leen M 't Hart,Robert L. Hanson,Timothy M. Frayling +55 more
TL;DR: The largest genome-wide association study of first-phase insulin secretion, as measured by intravenous glucose tolerance tests, using up to 5,567 individuals without diabetes from 10 studies is performed, providing further insight into the mechanisms by which common genetic variation influences type 2 diabetes risk and glycemic traits.