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성함이나 학술지명, PMID로 찾아보십시오.
Jain D에 대해
16건.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Hu Y,
Stilp AM,
McHugh CP,
Rao S,
Jain D,
Zheng X,
Lane J,
Méric de Bellefon S,
Raffield LM,
Chen MH,
Yanek LR,
Wheeler M
외 67명 — 모두 보기
Yao Y,
Ren C,
Broome J,
Moon JY,
de Vries PS,
Hobbs BD,
Sun Q,
Surendran P,
Brody JA,
Blackwell TW,
Choquet H,
Ryan K,
Duggirala R,
Heard-Costa N,
Wang Z,
Chami N,
Preuss MH,
Min N,
Ekunwe L,
Lange LA,
Cushman M,
Faraday N,
Curran JE,
Almasy L,
Kundu K,
Smith AV,
Gabriel S,
Rotter JI,
Fornage M,
Lloyd-Jones DM,
Vasan RS,
Smith NL,
North KE,
Boerwinkle E,
Becker LC,
Lewis JP,
Abecasis GR,
Hou L,
O'Connell JR,
Morrison AC,
Beaty TH,
Kaplan R,
Correa A,
Blangero J,
Jorgenson E,
Psaty BM,
Kooperberg C,
Walton RT,
Kleinstiver BP,
Tang H,
Loos RJF,
Soranzo N,
Butterworth AS,
Nickerson D,
Rich SS,
Mitchell BD,
Johnson AD,
Auer PL,
Li Y,
Mathias RA,
Lettre G,
Pankratz N,
Laurie CC,
Laurie CA,
Bauer DE,
Conomos MP,
Reiner AP
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
페이지 12개+
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals
Tahir UA,
Katz DH,
Avila-Pachecho J,
Bick AG,
Pampana A,
Robbins JM,
Yu Z,
Chen ZZ,
Benson MD,
Cruz DE,
Ngo D,
Deng S
외 27명 — 모두 보기
Shi X,
Zheng S,
Eisman AS,
Farrell L,
Hall ME,
Correa A,
Tracy RP,
Durda P,
Taylor KD,
Liu Y,
Johnson WC,
Guo X,
Yao J,
Chen YI,
Manichaikul AW,
Ruberg FL,
Blaner WS,
Jain D,
Bouchard C,
Sarzynski MA,
Rich SS,
Rotter JI,
Wang TJ,
Wilson JG,
Clish CB,
Natarajan P,
Gerszten RE
NHLBI Trans-Omics for Precision Medicine 1 Consortium
Nature communications · 2022 · PMID 35995766 · open access
페이지 12개+
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos
Hodonsky CJ,
Jain D,
Schick UM,
Morrison JV,
Brown L,
McHugh CP,
Schurmann C,
Chen DD,
Liu YM,
Auer PL,
Laurie CA,
Taylor KD
외 15명 — 모두 보기
Browning BL,
Li Y,
Papanicolaou G,
Rotter JI,
Kurita R,
Nakamura Y,
Browning SR,
Loos RJF,
North KE,
Laurie CC,
Thornton TA,
Pankratz N,
Bauer DE,
Sofer T,
Reiner AP
PLoS genetics · 2017 · PMID 28453575 · open access
페이지 4개
GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos
Sanders AE,
Jain D,
Sofer T,
Kerr KF,
Laurie CC,
Shaffer JR,
Marazita ML,
Kaste LM,
Slade GD,
Fillingim RB,
Ohrbach R,
Maixner W
외 15명 — 모두 보기
Kocher T,
Bernhardt O,
Teumer A,
Schwahn C,
Sipilä K,
Lähdesmäki R,
Männikkö M,
Pesonen P,
Järvelin M,
Rizzatti-Barbosa CM,
Meloto CB,
Ribeiro-Dasilva M,
Diatchenko L,
Serrano P,
Smith SB
Journal of dental research · 2017 · PMID 28081371
페이지 3개
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos
Jain D,
Hodonsky CJ,
Schick UM,
Morrison JV,
Minnerath S,
Brown L,
Schurmann C,
Liu Y,
Auer PL,
Laurie CA,
Taylor KD,
Browning BL
외 9명 — 모두 보기
Human molecular genetics · 2017 · PMID 28158719
페이지 3개
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
외 66명 — 모두 보기
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
페이지 3개
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
Leslie EJ,
Carlson JC,
Shaffer JR,
Feingold E,
Wehby G,
Laurie CA,
Jain D,
Laurie CC,
Doheny KF,
McHenry T,
Resick J,
Sanchez C
외 43명 — 모두 보기
Jacobs J,
Emanuele B,
Vieira AR,
Neiswanger K,
Lidral AC,
Valencia-Ramirez LC,
Lopez-Palacio AM,
Valencia DR,
Arcos-Burgos M,
Czeizel AE,
Field LL,
Padilla CD,
Cutiongco-de la Paz EM,
Deleyiannis F,
Christensen K,
Munger RG,
Lie RT,
Wilcox A,
Romitti PA,
Castilla EE,
Mereb JC,
Poletta FA,
Orioli IM,
Carvalho FM,
Hecht JT,
Blanton SH,
Buxó CJ,
Butali A,
Mossey PA,
Adeyemo WL,
James O,
Braimah RO,
Aregbesola BS,
Eshete MA,
Abate F,
Koruyucu M,
Seymen F,
Ma L,
de Salamanca JE,
Weinberg SM,
Moreno L,
Murray JC,
Marazita ML
Human molecular genetics · 2016 · PMID 27033726
페이지 2개
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
Iotchkova V,
Huang J,
Morris JA,
Jain D,
Barbieri C,
Walter K,
Min JL,
Chen L,
Astle W,
Cocca M,
Deelen P,
Elding H
외 55명 — 모두 보기
Farmaki AE,
Franklin CS,
Franberg M,
Gaunt TR,
Hofman A,
Jiang T,
Kleber ME,
Lachance G,
Luan J,
Malerba G,
Matchan A,
Mead D,
Memari Y,
Ntalla I,
Panoutsopoulou K,
Pazoki R,
Perry JRB,
Rivadeneira F,
Sabater-Lleal M,
Sennblad B,
Shin SY,
Southam L,
Traglia M,
van Dijk F,
van Leeuwen EM,
Zaza G,
Zhang W,
Amin N,
Butterworth A,
Chambers JC,
Dedoussis G,
Dehghan A,
Franco OH,
Franke L,
Frontini M,
Gambaro G,
Gasparini P,
Hamsten A,
Issacs A,
Kooner JS,
Kooperberg C,
Langenberg C,
Marz W,
Scott RA,
Swertz MA,
Toniolo D,
Uitterlinden AG,
van Duijn CM,
Watkins H,
Zeggini E,
Maurano MT,
Timpson NJ,
Reiner AP,
Auer PL,
Soranzo N
UK10K Consortium
Nature genetics · 2016 · PMID 27668658
페이지 2개
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Little A,
Hu Y,
Sun Q,
Jain D,
Broome J,
Chen MH,
Thibord F,
McHugh C,
Surendran P,
Blackwell TW,
Brody JA,
Bhan A
외 55명 — 모두 보기
Chami N,
de Vries PS,
Ekunwe L,
Heard-Costa N,
Hobbs BD,
Manichaikul A,
Moon JY,
Preuss MH,
Ryan K,
Wang Z,
Wheeler M,
Yanek LR,
Abecasis GR,
Almasy L,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Choquet H,
Correa A,
Curran JE,
Faraday N,
Fornage M,
Glahn DC,
Hou L,
Jorgenson E,
Kooperberg C,
Lewis JP,
Lloyd-Jones DM,
Loos RJF,
Min YI,
Mitchell BD,
Morrison AC,
Nickerson DA,
North KE,
O'Connell JR,
Pankratz N,
Psaty BM,
Vasan RS,
Rich SS,
Rotter JI,
Smith AV,
Smith NL,
Tang H,
Tracy RP,
Conomos MP,
Laurie CA,
Mathias RA,
Li Y,
Auer PL,
Thornton T,
Reiner AP,
Johnson AD,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Human molecular genetics · 2022 · PMID 34553764
페이지 2개
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
외 113명 — 모두 보기
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
페이지 2개
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
Schick UM,
Jain D,
Hodonsky CJ,
Morrison JV,
Davis JP,
Brown L,
Sofer T,
Conomos MP,
Schurmann C,
McHugh CP,
Nelson SC,
Vadlamudi S
외 26명 — 모두 보기
Stilp A,
Plantinga A,
Baier L,
Bien SA,
Gogarten SM,
Laurie CA,
Taylor KD,
Liu Y,
Auer PL,
Franceschini N,
Szpiro A,
Rice K,
Kerr KF,
Rotter JI,
Hanson RL,
Papanicolaou G,
Rich SS,
Loos RJ,
Browning BL,
Browning SR,
Weir BS,
Laurie CC,
Mohlke KL,
North KE,
Thornton TA,
Reiner AP
American journal of human genetics · 2016 · PMID 26805783
페이지 1개
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Leslie EJ,
Liu H,
Carlson JC,
Shaffer JR,
Feingold E,
Wehby G,
Laurie CA,
Jain D,
Laurie CC,
Doheny KF,
McHenry T,
Resick J
외 46명 — 모두 보기
Sanchez C,
Jacobs J,
Emanuele B,
Vieira AR,
Neiswanger K,
Standley J,
Czeizel AE,
Deleyiannis F,
Christensen K,
Munger RG,
Lie RT,
Wilcox A,
Romitti PA,
Field LL,
Padilla CD,
Cutiongco-de la Paz EM,
Lidral AC,
Valencia-Ramirez LC,
Lopez-Palacio AM,
Valencia DR,
Arcos-Burgos M,
Castilla EE,
Mereb JC,
Poletta FA,
Orioli IM,
Carvalho FM,
Hecht JT,
Blanton SH,
Buxó CJ,
Butali A,
Mossey PA,
Adeyemo WL,
James O,
Braimah RO,
Aregbesola BS,
Eshete MA,
Deribew M,
Koruyucu M,
Seymen F,
Ma L,
de Salamanca JE,
Weinberg SM,
Moreno L,
Cornell RA,
Murray JC,
Marazita ML
American journal of human genetics · 2016 · PMID 27018472
페이지 1개
Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts
Kerr KF,
Avery CL,
Lin HJ,
Raffield LM,
Zhang QS,
Browning BL,
Browning SR,
Conomos MP,
Gogarten SM,
Laurie CC,
Sofer T,
Thornton TA
외 20명 — 모두 보기
Hohensee C,
Jackson RD,
Kooperberg C,
Li Y,
Méndez-Giráldez R,
Perez MV,
Peters U,
Reiner AP,
Zhang ZM,
Yao J,
Sotoodehnia N,
Taylor KD,
Guo X,
Lange LA,
Soliman EZ,
Wilson JG,
Rotter JI,
Heckbert SR,
Jain D,
Whitsel EA
Heart rhythm · 2017 · PMID 28610988
페이지 1개
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A<sub>1c</sub> With Implications for Glycemic Status in U.S. Hispanics/Latinos
Moon JY,
Louie TL,
Jain D,
Sofer T,
Schurmann C,
Below JE,
Lai CQ,
Aviles-Santa ML,
Talavera GA,
Smith CE,
Petty LE,
Bottinger EP
외 13명 — 모두 보기
Chen YI,
Taylor KD,
Daviglus ML,
Cai J,
Wang T,
Tucker KL,
Ordovás JM,
Hanis CL,
Loos RJF,
Schneiderman N,
Rotter JI,
Kaplan RC,
Qi Q
Diabetes care · 2019 · PMID 31213470
페이지 1개
Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
Sarnowski C,
Chen H,
Biggs ML,
Wassertheil-Smoller S,
Bressler J,
Irvin MR,
Ryan KA,
Karasik D,
Arnett DK,
Cupples LA,
Fardo DW,
Gogarten SM
외 16명 — 모두 보기
Heavner BD,
Jain D,
Kang HM,
Kooperberg C,
Mainous AG,
Mitchell BD,
Morrison AC,
O'Connell JR,
Psaty BM,
Rice K,
Smith AV,
Vasan RS,
Windham BG,
Kiel DP,
Murabito JM,
Lunetta KL
TOPMed Longevity and Healthy Aging Working Group · from the NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
PloS one · 2021 · PMID 34214102 · open access
페이지 1개
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Mikhaylova AV,
McHugh CP,
Polfus LM,
Raffield LM,
Boorgula MP,
Blackwell TW,
Brody JA,
Broome J,
Chami N,
Chen MH,
Conomos MP,
Cox C
외 81명 — 모두 보기
Curran JE,
Daya M,
Ekunwe L,
Glahn DC,
Heard-Costa N,
Highland HM,
Hobbs BD,
Ilboudo Y,
Jain D,
Lange LA,
Miller-Fleming TW,
Min N,
Moon JY,
Preuss MH,
Rosen J,
Ryan K,
Smith AV,
Sun Q,
Surendran P,
de Vries PS,
Walter K,
Wang Z,
Wheeler M,
Yanek LR,
Zhong X,
Abecasis GR,
Almasy L,
Barnes KC,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Chavan S,
Cho MH,
Choquet H,
Correa A,
Cox N,
DeMeo DL,
Faraday N,
Fornage M,
Gerszten RE,
Hou L,
Johnson AD,
Jorgenson E,
Kaplan R,
Kooperberg C,
Kundu K,
Laurie CA,
Lettre G,
Lewis JP,
Li B,
Li Y,
Lloyd-Jones DM,
Loos RJF,
Manichaikul A,
Meyers DA,
Mitchell BD,
Morrison AC,
Ngo D,
Nickerson DA,
Nongmaithem S,
North KE,
O'Connell JR,
Ortega VE,
Pankratz N,
Perry JA,
Psaty BM,
Rich SS,
Soranzo N,
Rotter JI,
Silverman EK,
Smith NL,
Tang H,
Tracy RP,
Thornton TA,
Vasan RS,
Zein J,
Mathias RA,
Reiner AP,
Auer PL
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
페이지 1개
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제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.