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Roberts DJ에 대해
14건.
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Astle WJ,
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외 62명 — 모두 보기
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Cell · 2016 · PMID 27863252 · open access
페이지 12개+
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Turcot V,
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외 390명 — 모두 보기
Karaderi T,
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CHD Exome+ Consortium · EPIC-CVD Consortium 외 컨소시엄 9곳
Nature genetics · 2018 · PMID 29273807 · open access
페이지 12개+
Genomic atlas of the human plasma proteome
Sun BB,
Maranville JC,
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Stacey D,
Staley JR,
Blackshaw J,
Burgess S,
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외 21명 — 모두 보기
Prins BP,
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Nature · 2018 · PMID 29875488
페이지 12개+
A catalog of genetic loci associated with kidney function from analyses of a million individuals
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외 315명 — 모두 보기
Chai JF,
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Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
페이지 12개+
Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income
Hill WD,
Davies NM,
Ritchie SJ,
Skene NG,
Bryois J,
Bell S,
Di Angelantonio E,
Roberts DJ,
Xueyi S,
Davies G,
Liewald DCM,
Porteous DJ
외 5명 — 모두 보기
Nature communications · 2019 · PMID 31844048 · open access
페이지 12개+
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen MH,
Raffield LM,
Mousas A,
Sakaue S,
Huffman JE,
Moscati A,
Trivedi B,
Jiang T,
Akbari P,
Vuckovic D,
Bao EL,
Zhong X
외 98명 — 모두 보기
Manansala R,
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Huang QQ,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
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Koskeridis F,
Lange LA,
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Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Martin HC,
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VA Million Veteran Program
Cell · 2020 · PMID 32888493
페이지 12개+
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic D,
Bao EL,
Akbari P,
Lareau CA,
Mousas A,
Jiang T,
Chen MH,
Raffield LM,
Tardaguila M,
Huffman JE,
Ritchie SC,
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외 100명 — 모두 보기
Ponstingl H,
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Dimou N,
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Broer L,
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Guo MH,
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Howson JMM,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
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Lehtimäki T,
Linneberg A,
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Matsuda K,
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Nadkarni GN,
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Raitakari OT,
Rich SS,
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Cho K,
Li Y,
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Okada Y,
Roberts DJ,
Inouye M,
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Lettre G,
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VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
페이지 12개+
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Akbari P,
Vuckovic D,
Stefanucci L,
Jiang T,
Kundu K,
Kreuzhuber R,
Bao EL,
Collins JH,
Downes K,
Grassi L,
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Kaptoge S
외 20명 — 모두 보기
Knight JC,
Meacham S,
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Seyres D,
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Walter K,
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Nature communications · 2023 · PMID 37596262 · open access
페이지 12개+
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Schormair B,
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Bell S,
Didriksen M,
Nawaz MS,
Schandra N,
Stefani A,
Högl B,
Dauvilliers Y,
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외 55명 — 모두 보기
Paulus W,
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23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
페이지 12개+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
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외 60명 — 모두 보기
Bonglack E,
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DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
페이지 12개+
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis
Wheeler E,
Leong A,
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Strawbridge RJ,
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외 203명 — 모두 보기
Wang X,
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Wong TY,
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Meigs JB
EPIC-CVD Consortium · EPIC-InterAct Consortium 외 컨소시엄 1곳
PLoS medicine · 2017 · PMID 28898252 · open access
페이지 10개
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Schormair B,
Zhao C,
Bell S,
Tilch E,
Salminen AV,
Pütz B,
Dauvilliers Y,
Stefani A,
Högl B,
Poewe W,
Kemlink D,
Sonka K
외 39명 — 모두 보기
Bachmann CG,
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek Z,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Allen RP,
Earley CJ,
Ondo WG,
Xiong L,
Montplaisir J,
Gan-Or Z,
Perola M,
Vodicka P,
Dina C,
Franke A,
Tittmann L,
Stewart AFR,
Shah SH,
Gieger C,
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Rouleau GA,
Berger K,
Oexle K,
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Hinds DA,
Müller-Myhsok B,
Winkelmann J
23andMe Research Team · DESIR study group
The Lancet. Neurology · 2017 · PMID 29029846 · open access
페이지 10개
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
Ji SG,
Juran BD,
Mucha S,
Folseraas T,
Jostins L,
Melum E,
Kumasaka N,
Atkinson EJ,
Schlicht EM,
Liu JZ,
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외 58명 — 모두 보기
Boberg KM,
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Lazaridis KN,
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UK-PSC Consortium · International IBD Genetics Consortium 외 컨소시엄 1곳
Nature genetics · 2017 · PMID 27992413 · open access
페이지 8개
Large genome-wide association study identifies three novel risk variants for restless legs syndrome
Didriksen M,
Nawaz MS,
Dowsett J,
Bell S,
Erikstrup C,
Pedersen OB,
Sørensen E,
Jennum PJ,
Burgdorf KS,
Burchell B,
Butterworth AS,
Soranzo N
외 22명 — 모두 보기
Rye DB,
Trotti LM,
Saini P,
Stefansdottir L,
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Thorleifsson G,
Sigmundsson T,
Sigurdsson AP,
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Tanck MWT,
Ouwehand WH,
Roberts DJ,
Earley EJ,
Busch MP,
Mast AE,
Page GP,
Danesh J,
Di Angelantonio E,
Stefansson H,
Ullum H,
Stefansson K
Communications biology · 2020 · PMID 33239738 · open access
페이지 1개
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