J
Jeffrey C. Murray
Researcher at Roy J. and Lucille A. Carver College of Medicine
Publications - 65
Citations - 2935
Jeffrey C. Murray is an academic researcher from Roy J. and Lucille A. Carver College of Medicine. The author has contributed to research in topics: Population & Single-nucleotide polymorphism. The author has an hindex of 30, co-authored 65 publications receiving 2598 citations. Previous affiliations of Jeffrey C. Murray include Bill & Melinda Gates Foundation & Boston Children's Hospital.
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Journal ArticleDOI
Noninvasive Whole-Genome Sequencing of a Human Fetus
Jacob O. Kitzman,Matthew W. Snyder,Mario Ventura,Alexandra P. Lewis,Ruolan Qiu,La Vone E Simmons,Hilary S. Gammill,Craig E. Rubens,Donna A. Santillan,Jeffrey C. Murray,Holly K. Tabor,Michael J. Bamshad,Evan E. Eichler,Jay Shendure +13 more
TL;DR: Combining genome sequencing of two parents, genome-wide maternal haplotyping, and deep sequencing of maternal plasma DNA to noninvasively determine the genome sequence of a human fetus at 18.5 weeks of gestation hints that comprehensive, noninvasive prenatal screening for Mendelian disorders may be clinically feasible in the near future.
Journal ArticleDOI
Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation births.
Nansi S. Boghossian,Grier P. Page,Edward F. Bell,Barbara J. Stoll,Jeffrey C. Murray,C. Michael Cotten,Seetha Shankaran,Michele C. Walsh,Abbot R. Laptook,Nancy S. Newman,Ellen C. Hale,Scott A. McDonald,Abhik Das,Rosemary D. Higgins +13 more
TL;DR: In this paper, the incidence of late-onset sepsis and demographic and clinical characteristics associated with LOS in very low birth weight (VLBW) infants from singleton and multiple births, and examined the heritability of susceptibility to LOS among VLBW twins by comparing same-sex and unlike-sex twin pairs.
Journal ArticleDOI
Maternal Contributions to Preterm Delivery
TL;DR: The substantial portion of PTD risk explained by effects passed through the female line suggests a role for either imprinting or mitochondrial inheritance.
Journal ArticleDOI
Common variants at 12q15 and 12q24 are associated with infant head circumference
H. Rob Taal,Beate St Pourcain,Elisabeth Thiering,Shikta Das,Dennis O. Mook-Kanamori,Dennis O. Mook-Kanamori,Nicole M. Warrington,Nicole M. Warrington,Marika Kaakinen,Eskil Kreiner-Møller,Jonathan P. Bradfield,Rachel M. Freathy,Rachel M. Freathy,Frank Geller,Mònica Guxens,Diana L. Cousminer,Marjan Kerkhof,Nicholas J. Timpson,M. Arfan Ikram,Lawrence J. Beilin,Klaus Bønnelykke,Jessica L. Buxton,Pimphen Charoen,Pimphen Charoen,Bo L. Chawes,Johan G. Eriksson,Johan G. Eriksson,David M. Evans,Albert Hofman,John P. Kemp,Cecilia E. Kim,Norman Klopp,Jari Lahti,Stephen J. Lye,George McMahon,Frank D. Mentch,Martina Müller-Nurasyid,Paul F. O'Reilly,Inga Prokopenko,Fernando Rivadeneira,Eric A.P. Steegers,Jordi Sunyer,Carla M. T. Tiesler,Hanieh Yaghootkar,Myriam Fornage,Albert V. Smith,Albert V. Smith,Sudha Seshadri,Reinhold Schmidt,Reinhold Schmidt,Stéphanie Debette,Stéphanie Debette,Stéphanie Debette,Henri Vrooman,Henri Vrooman,Sigurdur Sigurdsson,Stefan Ropele,Laura H. Coker,W. T. Longstreth,W. T. Longstreth,Wiro J. Niessen,Wiro J. Niessen,Wiro J. Niessen,Anita L. DeStefano,Anita L. DeStefano,Alexa S. Beiser,Alexa S. Beiser,Alex P. Zijdenbos,Maksim Struchalin,Clifford R. Jack,Michael A. Nalls,Rhoda Au,Rhoda Au,Haukur Gudnason,Aad van der Lugt,Tamara B. Harris,William M. Meeks,Meike W. Vernooij,Mark A. van Buchem,Diane J. Catellier,Vilmundur Gudnason,Vilmundur Gudnason,B. Gwen Windham,Philip A. Wolf,Cornelia M. van Duijn,Thomas H. Mosley,Thomas H. Mosley,Helena Schmidt,Lenore J. Launer,Lenore J. Launer,Monique M.B. Breteler,Wei Ang,Toos C. E. M. van Beijsterveldt,Toos C. E. M. van Beijsterveldt,Nienke E. Bergen,Kelly S. Benke,Diane Berry,Lachlan J. M. Coin,Paul Elliott,Timothy M. Frayling,Romy Gaillard,Maria M. Groen-Blokhuis,Maria M. Groen-Blokhuis,Dexter Hadley,Jouke-Jan Hottenga,Ville Huikari,Elina Hyppönen,Elina Hyppönen,Matthew Kowgier,Debbie A Lawlor,Alex Lewin,Cecilia M. Lindgren,Julie A. Marsh,Christel M. Middeldorp,Iona Y. Millwood,Iona Y. Millwood,Michel G. Nivard,Lyle J. Palmer,Lyle J. Palmer,Alina Rodriguez,Alina Rodriguez,Alina Rodriguez,Sylvain Sebert,Ulla Sovio,Ulla Sovio,Marie Standl,David P. Strachan,André G. Uitterlinden,Beatriz Valcarcel,Scott W. White,Gonneke Willemsen,Dorret I. Boomsma,Xavier Estivill,Struan F.A. Grant,Andrew T. Hattersley,Joachim Heinrich,Vincent W. V. Jaddoe,Marjo-Riitta Järvelin,Mark I. McCarthy,Craig E. Pennell,C Power,E. Widen,E. Widen,Alexandra I. F. Blakemore,Rosetta M. Chiavacci,Bjarke Feenstra,Julio Fernandez-Banet,Anna-Liisa Hartikainen,Albert J. van der Heijden,Carmen Iñiguez,Mark Lathrop,Wendy L. McArdle,Anne Mølgaard,John P. Newnham,Aarno Palotie,Aarno Palotie,Aarno Palotie,A Pouta,A Pouta,Susan M. Ring,H.-Erich Wichmann,Nadja Hawwa Vissing,Charles DeCarli,Charles DeCarli,Gerard H. Koppelman,Mads Melbye,Hans Bisgaard,Hakon Hakonarson,Hakon Hakonarson,Hakon Hakonarson,George Davey Smith,George Davey Smith,Linda S. Adair,Mustafa Atalay,Oliver S. P. Davis,Claudia Flexeder,Liang Kee Goh,Liang Kee Goh,Claire M. A. Haworth,Johannes Hedebrand,Anke Hinney,Joel N. Hirschhorn,Joel N. Hirschhorn,Joel N. Hirschhorn,John W. Holloway,Claus Holst,Momoko Horikoshi,Tuomas O. Kilpeläinen,Mirna Kirin,Hanna Maaria Lakka,Leslie A. Lange,Terho Lehtimäki,Terho Lehtimäki,Virpi Lindi,Reedik Maggi,Reedik Maggi,Jeffrey C. Murray,Ellen Aagaard Nohr,Ioanna Ntalla,Emily Oken,Emily Oken,Emily Oken,Kalliope Panoutsopoulou,Jennifer Pararajasingham,Rany M. Salem,Rany M. Salem,Rany M. Salem,Niina Siitonen,Yik Y. Teo,Eleftheria Zeggini,Cyrus Cooper,Matthew H. Gillman,Berthold Hocher,Berthold Hocher,Timo A. Lakka,Karen L. Mohlke,George Dedoussis,Ken K. Ong,Ewan R. Pearson,Thomas S. Price,Olli T. Raitakari,Olli T. Raitakari,Seang-Mei Saw,André Scherag,Olli Simell,Olli Simell,Thorkild I.A. Sørensen,Thorkild I.A. Sørensen,James F. Wilson,James F. Wilson,James F. Wilson +230 more
TL;DR: This article performed a meta-analysis of seven genome-wide association studies (GWAS) (N = 10,768 individuals of European ancestry enrolled in pregnancy and/or birth cohorts) and followed up three lead signals in six replication studies (combined N = 19,089).
Common variants at 12q15 and 12q24 are associated with infant head circumference
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,Frank Geller,Mònica Guxens,Diana L. Cousminer,Marjan Kerkhof,Nicholas J. Timpson,M. Arfan Ikram,Lawrence J. Beilin,Klaus Bønnelykke,Jessica L. Buxton,Pimphen Charoen,Bo L. Chawes,Johan G. Eriksson,David M. Evans,Albert Hofman,John P. Kemp,Cecilia E. Kim,Norman Klopp,Jari Lahti,Stephen J. Lye,George McMahon,Frank D. Mentch,Martina Mueller-Nurasyid,Paul F. O'Reilly,Inga Prokopenko,Fernando Rivadeneira,Eric A.P. Steegers,Jordi Sunyer,Carla M. T. Tiesler,Hanieh Yaghootkar,Monique M.B. Breteler,Stéphanie Debette,Myriam Fornage,Vilmundur Gudnason,Lenore J. Launer,Aad van der Lugt,Thomas H. Mosley,Sudha Seshadri,Albert V. Smith,Meike W. Vernooij,Alexandra I. F. Blakemore,Rosetta M. Chiavacci,Bjarke Feenstra,Julio Fernandez-Banet,Struan F.A. Grant,Anna-Liisa Hartikainen,Albert J. van der Heijden,Carmen Iñiguez,Mark Lathrop,Wendy L. McArdle,Anne Mølgaard,John P. Newnham,Lyle J. Palmer,Aarno Palotie,A Pouta,Susan M. Ring,Ulla Sovio,Marie Standl,André G. Uitterlinden,H-Erich Wichmann,Nadja Hawwa Vissing,Charles DeCarli,Cornelia M. van Duijn,Mark I. McCarthy,Gerard H. Koppelman,Xavier Estivill,Andrew T. Hattersley,Mads Melbye,Hans Bisgaard,Craig E. Pennell,Elisabeth Widen,Hakon Hakonarson,George Davey Smith,Joachim Heinrich,Marjo-Riitta Järvelin,Vincent W. V. Jaddoe,Linda S. Adair,Wei Ang,Mustafa Atalay,Toos C. E. M. van Beijsterveldt,Nienke E. Bergen,Kelly S. Benke,Diane J. Berry,Lachlan J. M. Coin,Oliver S. P. Davis,Paul Elliott,Claudia Flexeder,Timothy M. Frayling,Romy Gaillard,Maria M. Groen-Blokhuis,Liang Kee Goh,Claire M. A. Haworth,Dexter Hadley,Johannes Hedebrand,Anke Hinney,Joel N. Hirschhorn,John W. Holloway,Claus Holst,Jouke-Jan Hottenga,Momoko Horikoshi,Ville Huikari,Elina Hyppönen,Tuomas O. Kilpeläinen,Mirna Kirin,Matthew Kowgier,Hanna-Maaria Lakka,Leslie A. Lange,Debbie A Lawlor,Terho Lehtimäki,Alex Lewin,Cecilia M. Lindgren,Virpi Lindi,Reedik Maggi,Julie A. Marsh,Christel M. Middeldorp,Iona Y. Millwood,Jeffrey C. Murray,Michel G. Nivard,Ellen A. Nohr,Ioanna Ntalla,Emily Oken,Kalliope Panoutsopoulou,Jennifer Pararajasingham,Alina Rodriguez,Rany M. Salem,Sylvain Sebert,Niina Siitonen,David P. Strachan,Yik Ying Teo,Beatriz Valcarcel,Scott W. White,Gonneke Willemsen,Eleftheria Zeggini,Dorret I. Boomsma,Cyrus Cooper,Matthew W. Gillman,Berthold Hocher,Timo A. Lakka,Karen L. Mohlke,George Dedoussis,Ken K. Ong,Ewan R. Pearson,Thomas S. Price,Chris Power,Olli T. Raitakari,Seang-Mei Saw,André Scherag,Olli Simell,Thorkild I. A. Sørensen,James F. Wilson,Reinhold E. Schmidt,Henri A. Vrooman,Sigurdur Sigurdsson,Stefan Ropele,Laura H. Coker,W. T. Longstreth,Wiro J. Niessen,Anita L. DeStefano,Alexa S. Beiser,Alex P. Zijdenbos,Maksim Struchalin,Clifford R. Jack,Mike A. Nalls,Rhoda Au,Haukur Gudnason,Tamara B. Harris,William M. Meeks,Mark A. van Buchem,Diane J. Catellier,B. Gwen Windham,Philip A. Wolf,Helena Schmidt +180 more
TL;DR: A meta-analysis of genome-wide association studies and lead signals showed suggestive evidence of association with head circumference in infancy, indicating that a common genetic variant in this region might link early brain growth with neurological disease in later life.