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성함이나 학술지명, PMID로 찾아보십시오.
Rich SS에 대해
75건, 그중 15건 표시.
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
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
외 55명 — 모두 보기
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
페이지 1개
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations
Hu Y,
Tanaka T,
Zhu J,
Guan W,
Wu JHY,
Psaty BM,
McKnight B,
King IB,
Sun Q,
Richard M,
Manichaikul A,
Frazier-Wood AC
외 21명 — 모두 보기
Kabagambe EK,
Hopkins PN,
Ordovas JM,
Ferrucci L,
Bandinelli S,
Arnett DK,
Chen YI,
Liang S,
Siscovick DS,
Tsai MY,
Rich SS,
Fornage M,
Hu FB,
Rimm EB,
Jensen MK,
Lemaitre RN,
Mozaffarian D,
Steffen LM,
Morris AP,
Li H,
Lin X
Journal of lipid research · 2017 · PMID 28298293 · open access
페이지 1개
A Genome-Wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos
Burkart KM,
Sofer T,
London SJ,
Manichaikul A,
Hartwig FP,
Yan Q,
Soler Artigas M,
Avila L,
Chen W,
Davis Thomas S,
Diaz AA,
Hall IP
외 14명 — 모두 보기
Horta BL,
Kaplan RC,
Laurie CC,
Menezes AM,
Morrison JV,
Oelsner EC,
Rastogi D,
Rich SS,
Soto-Quiros M,
Stilp AM,
Tobin MD,
Wain LV,
Celedón JC,
Barr RG
American journal of respiratory and critical care medicine · 2018 · PMID 29394082
페이지 1개
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
Ahlqvist E,
Sandholm N,
Deshmukh H,
Rayner NW,
Abdalla M,
Ladenvall C,
Ziemek D,
Fauman E,
Robertson NR,
McKeigue PM,
Valo E
외 69명 — 모두 보기
Forsblom C,
Harjutsalo V,
Perna A,
Rurali E,
Marcovecchio ML,
Igo RP Jr,
Salem RM,
Perico N,
Lajer M,
Käräjämäki A,
Imamura M,
Kubo M,
Takahashi A,
Sim X,
Liu J,
van Dam RM,
Jiang G,
Tam CHT,
Luk AOY,
Lee HM,
Lim CKP,
Szeto CC,
So WY,
Chan JCN,
Ang SF,
Dorajoo R,
Wang L,
Clara TSH,
McKnight AJ,
Duffy S,
Pezzolesi MG,
Marre M,
Gyorgy B,
Hadjadj S,
Hiraki LT,
Ahluwalia TS,
Almgren P,
Schulz CA,
Orho-Melander M,
Linneberg A,
Christensen C,
Witte DR,
Grarup N,
Brandslund I,
Melander O,
Paterson AD,
Tregouet D,
Maxwell AP,
Lim SC,
Ma RCW,
Tai ES,
Maeda S,
Lyssenko V,
Tuomi T,
Krolewski AS,
Rich SS,
Hirschhorn JN,
Florez JC,
Dunger D,
Pedersen O,
Hansen T,
Rossing P,
Remuzzi G,
Brosnan MJ,
Palmer CNA,
Groop PH,
Colhoun HM,
Groop LC,
McCarthy MI
Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group 외 컨소시엄 4곳
Diabetes · 2018 · PMID 29703844
페이지 1개
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Jackson VE,
Latourelle JC,
Wain LV,
Smith AV,
Grove ML,
Bartz TM,
Obeidat M,
Province MA,
Gao W,
Qaiser B,
Porteous DJ,
Cassano PA
외 95명 — 모두 보기
Ahluwalia TS,
Grarup N,
Li J,
Altmaier E,
Marten J,
Harris SE,
Manichaikul A,
Pottinger TD,
Li-Gao R,
Lind-Thomsen A,
Mahajan A,
Lahousse L,
Imboden M,
Teumer A,
Prins B,
Lyytikäinen LP,
Eiriksdottir G,
Franceschini N,
Sitlani CM,
Brody JA,
Bossé Y,
Timens W,
Kraja A,
Loukola A,
Tang W,
Liu Y,
Bork-Jensen J,
Justesen JM,
Linneberg A,
Lange LA,
Rawal R,
Karrasch S,
Huffman JE,
Smith BH,
Davies G,
Burkart KM,
Mychaleckyj JC,
Bonten TN,
Enroth S,
Lind L,
Brusselle GG,
Kumar A,
Stubbe B,
Kähönen M,
Wyss AB,
Psaty BM,
Heckbert SR,
Hao K,
Rantanen T,
Kritchevsky SB,
Lohman K,
Skaaby T,
Pisinger C,
Hansen T,
Schulz H,
Polasek O,
Campbell A,
Starr JM,
Rich SS,
Mook-Kanamori DO,
Johansson Å,
Ingelsson E,
Uitterlinden AG,
Weiss S,
Raitakari OT,
Gudnason V,
North KE,
Gharib SA,
Sin DD,
Taylor KD,
O'Connor GT,
Kaprio J,
Harris TB,
Pederson O,
Vestergaard H,
Wilson JG,
Strauch K,
Hayward C,
Kerr S,
Deary IJ,
Barr RG,
de Mutsert R,
Gyllensten U,
Morris AP,
Ikram MA,
Probst-Hensch N,
Gläser S,
Zeggini E,
Lehtimäki T,
Strachan DP,
Dupuis J,
Morrison AC,
Hall IP,
Tobin MD,
London SJ
Understanding Society Scientific Group
Wellcome open research · 2018 · PMID 30175238 · open access
페이지 1개
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
외 290명 — 모두 보기
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Cooper RS,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
Kooner JS,
Laakso M,
Laurie CC,
Lee IT,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
Rauramaa R,
Redline S,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang JS,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Franceschini N,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Rice K,
Munroe PB,
Morrison AC,
Rao DC,
Rotimi CN,
Cupples LA
COGENT-Kidney Consortium · EPIC-InterAct Consortium 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30926973 · open access
페이지 1개
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis
Hobbs BD,
Putman RK,
Araki T,
Nishino M,
Gudmundsson G,
Gudnason V,
Eiriksdottir G,
Zilhao Nogueira NR,
Dupuis J,
Xu H,
O'Connor GT,
Manichaikul A
외 30명 — 모두 보기
Nguyen J,
Podolanczuk AJ,
Madahar P,
Rotter JI,
Lederer DJ,
Barr RG,
Rich SS,
Ampleford EJ,
Ortega VE,
Peters SP,
O'Neal WK,
Newell JD Jr,
Bleecker ER,
Meyers DA,
Allen RJ,
Oldham JM,
Ma SF,
Noth I,
Jenkins RG,
Maher TM,
Hubbard RB,
Wain LV,
Fingerlin TE,
Schwartz DA,
Washko GR,
Rosas IO,
Silverman EK,
Hatabu H,
Cho MH,
Hunninghake GM
American journal of respiratory and critical care medicine · 2019 · PMID 31339356
페이지 1개
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke
Keene KL,
Hyacinth HI,
Bis JC,
Kittner SJ,
Mitchell BD,
Cheng YC,
Pare G,
Chong M,
O'Donnell M,
Meschia JF,
Chen WM,
Sale MM
외 35명 — 모두 보기
Rich SS,
Nalls MA,
Zonderman AB,
Evans MK,
Wilson JG,
Correa A,
Markus HS,
Traylor M,
Lewis CM,
Carty CL,
Reiner A,
Haessler J,
Langefeld CD,
Gottesman R,
Mosley TH,
Woo D,
Yaffe K,
Liu Y,
Longstreth WT,
Psaty BM,
Kooperberg C,
Lange LA,
Sacco R,
Rundek T,
Lee JM,
Cruchaga C,
Furie KL,
Arnett DK,
Benavente OR,
Grewal RP,
Peddareddygari LR,
Dichgans M,
Malik R,
Worrall BB,
Fornage M
COMPASS, SiGN, and METASTROKE Consortia
Stroke · 2020 · PMID 32693751
페이지 1개
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
Cade BE,
Lee J,
Sofer T,
Wang H,
Zhang M,
Chen H,
Gharib SA,
Gottlieb DJ,
Guo X,
Lane JM,
Liang J,
Lin X
외 27명 — 모두 보기
Mei H,
Patel SR,
Purcell SM,
Saxena R,
Shah NA,
Evans DS,
Hanis CL,
Hillman DR,
Mukherjee S,
Palmer LJ,
Stone KL,
Tranah GJ,
Abecasis GR,
Boerwinkle EA,
Correa A,
Cupples LA,
Kaplan RC,
Nickerson DA,
North KE,
Psaty BM,
Rotter JI,
Rich SS,
Tracy RP,
Vasan RS,
Wilson JG,
Zhu X,
Redline S
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Sleep Working Group
Genome medicine · 2021 · PMID 34446064 · open access
페이지 1개
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 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
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
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