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Papers共 123 篇Author StatisticsCo-AuthorSimilar Experts

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Rare Coding Variant Analysis for Human Diseases Across Biobanks and Ancestries
Sean J. Jurgens, Xin Wang, Seung Hoan Choi,Lu-Chen Weng,Satoshi Koyama,James P. Pirruccello, Trang Nguyen, Patrick Smadbeck, Dongkeun Jang,Mark Chaffin,Roddy Walsh,Carolina Roselli, Amanda L. Elliott, Leonoor F. J. M. Wijdeveld, Kiran J. Biddinger, Shinwan Kany,Joel T. Ramo,Pradeep Natarajan,Krishna G. Aragam,Jason Flannick, Noel P. Burtt,Connie R. Bezzina,Steven A. Lubitz,Kathryn L. Lunetta,Patrick T. Ellinor
NATURE GENETICS (2024)
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Mapping the Aetiological Foundations of the Heart Failure Spectrum Using Human Genetics
Albert Henry, Xiaodong Mo,Chris Finan,Mark D. Chaffin,Doug Speed,Hanane Issa,Spiros Denaxas,James S. Ware,Sean L. Zheng,Anders Malarstig,Jasmine Gratton,Isabelle Bond,Carolina Roselli,David Miller,Sandesh Chopade,A. Floriaan Schmidt,Erik Abner,Lance Adams,Charlotte Andersson,Krishna G. Aragam,Johan Ärnlöv,Geraldine Asselin,Anna Axelsson Raja,Joshua D. Backman,Traci M. Bartz,Kiran J. Biddinger,Mary L. Biggs,Heather L. Bloom,Eric Boersma,Jeffrey Brandimarto,Michael R. Brown,Søren Brunak,Mie Topholm Bruun,Leonard Buckbinder,Henning Bundgaard,David J. Carey,Daniel I. Chasman,Xing Chen,James P. Cook,Tomasz Czuba,Simon de Denus,Abbas Dehghan,Graciela E. Delgado,Alexander S. Doney,Marcus Dörr,Joseph Dowsett,Samuel C. Dudley,Gunnar Engström,Christian Erikstrup,Tõnu Esko,Eric H. Farber-Eger,Stephan B. Felix,Sarah Finer,Ian Ford,Mohsen Ghanbari,Sahar Ghasemi,Jonas Ghouse,Vilmantas Giedraitis,Franco Giulianini,John S. Gottdiener,Stefan Gross,Daníel F. Guðbjartsson,Hongsheng Gui,Rebecca Gutmann,Sara Hägg,Christopher M. Haggerty,Åsa K. Hedman,Anna Helgadottir,Harry Hemingway,Hans Hillege,Craig L. Hyde,Bitten Aagaard Jensen,J. Wouter Jukema,Isabella Kardys,Ravi Karra,Maryam Kavousi,Jorge R. Kizer,Marcus E. Kleber,Lars Køber,Andrea Koekemoer,Karoline Kuchenbaecker,Yi-Pin Lai,David Lanfear,Claudia Langenberg,Honghuang Lin,Lars Lind,Cecilia M. Lindgren,Peter P. Liu,Barry London,Brandon D. Lowery,Jian’an Luan,Steven A. Lubitz,Patrik Magnusson,Kenneth B. Margulies,Nicholas A. Marston,Hilary Martin,Winfried März,Olle Melander,Ify R. Mordi,Michael P. Morley,Andrew P. Morris,Alanna C. Morrison,Lori Morton,Michael W. Nagle,Christopher P. Nelson,Alexander Niessner,Teemu Niiranen,Raymond Noordam,Christoph Nowak,Michelle L. O’Donoghue,Sisse Rye Ostrowski,Anjali T. Owens,Colin N. A. Palmer,Guillaume Paré,Ole Birger Pedersen,Markus Perola,Marie Pigeyre,Bruce M. Psaty,Kenneth M. Rice,Paul M. Ridker,Simon P. R. Romaine,Jerome I. Rotter,Christian T. Ruff, Mark S. Sabatine,Neneh Sallah,Veikko Salomaa,Naveed Sattar,Alaa A. Shalaby,Akshay Shekhar,Diane T. Smelser,Nicholas L. Smith,Erik Sørensen,Sundararajan Srinivasan,Kari Stefansson,Garðar Sveinbjörnsson,Per Svensson,Mari-Liis Tammesoo,Jean-Claude Tardif,Maris Teder-Laving,Alexander Teumer,Guðmundur Thorgeirsson,Unnur Thorsteinsdottir,Christian Torp-Pedersen,Vinicius Tragante,Stella Trompet,Andre G. Uitterlinden,Henrik Ullum,Pim van der Harst,David van Heel,Jessica van Setten,Marion van Vugt,Abirami Veluchamy,Monique Verschuuren,Niek Verweij,Christoffer Rasmus Vissing,Uwe Völker,Adriaan A. Voors,Lars Wallentin,Yunzhang Wang,Peter E. Weeke,Kerri L. Wiggins,L. Keoki Williams,Yifan Yang,Bing Yu,Faiez Zannad, Chaoqun Zheng, Genes & Health Research Team,DBDS Genomic Consortium,Folkert W. Asselbergs,Thomas P. Cappola,Marie-Pierre Dubé,Michael E. Dunn,Chim C. Lang,Nilesh J. Samani,Svati Shah,Ramachandran S. Vasan,J. Gustav Smith,Hilma Holm,Sonia Shah,Patrick T. Ellinor,Aroon D. Hingorani,Quinn Wells, R. Thomas Lumbers, HERMES Consortium
medrxiv（2023）
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Author Statistics

#Papers: 126

#Citation: 7869

H-Index: 33

G-Index: 82

Sociability: 7

Diversity: 2

Activity: 107

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