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성함이나 학술지명, PMID로 찾아보십시오.
He R에 대해
67건, 그중 20건 표시.
An SCN9A channelopathy causes congenital inability to experience pain
Cox JJ,
Reimann F,
Nicholas AK,
Thornton G,
Roberts E,
Springell K,
Karbani G,
Jafri H,
Mannan J,
Raashid Y,
Al-Gazali L,
Hamamy H
외 7명 — 모두 보기
Nature · 2006 · PMID 17167479
페이지 1개
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
Moffatt MF,
Kabesch M,
Liang L,
Dixon AL,
Strachan D,
Heath S,
Depner M,
von Berg A,
Bufe A,
Rietschel E,
Heinzmann A,
Simma B
외 12명 — 모두 보기
Frischer T,
Willis-Owen SA,
Wong KC,
Illig T,
Vogelberg C,
Weiland SK,
von Mutius E,
Abecasis GR,
Farrall M,
Gut IG,
Lathrop GM,
Cookson WO
Nature · 2007 · PMID 17611496
페이지 1개
Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone
Paternoster L,
Lorentzon M,
Vandenput L,
Karlsson MK,
Ljunggren O,
Kindmark A,
Mellstrom D,
Kemp JP,
Jarett CE,
Holly JM,
Sayers A,
St Pourcain B
외 7명 — 모두 보기
PLoS genetics · 2010 · PMID 21124946 · open access
페이지 1개
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans
Reitz C,
Jun G,
Naj A,
Rajbhandary R,
Vardarajan BN,
Wang LS,
Valladares O,
Lin CF,
Larson EB,
Graff-Radford NR,
Evans D,
De Jager PL
외 30명 — 모두 보기
Crane PK,
Buxbaum JD,
Murrell JR,
Raj T,
Ertekin-Taner N,
Logue M,
Baldwin CT,
Green RC,
Barnes LL,
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Manly JJ,
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Kamboh MI,
Lopez OL,
Bennett DA,
Hendrie H,
Hall KS,
Goate AM,
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Kukull WA,
Foroud TM,
Haines JL,
Farrer LA,
Pericak-Vance MA,
Schellenberg GD,
Mayeux R
Alzheimer Disease Genetics Consortium
JAMA · 2013 · PMID 23571587
페이지 1개
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
Rothwell S,
Cooper RG,
Lundberg IE,
Miller FW,
Gregersen PK,
Bowes J,
Vencovsky J,
Danko K,
Limaye V,
Selva-O'Callaghan A,
Hanna MG,
Machado PM
외 24명 — 모두 보기
Pachman LM,
Reed AM,
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Cobb J,
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Myositis Genetics Consortium
Annals of the rheumatic diseases · 2016 · PMID 26362759
페이지 1개
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Sims R,
van der Lee SJ,
Naj AC,
Bellenguez C,
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외 437명 — 모두 보기
Heilmann-Heimbach S,
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Cairns NJ,
Cao C,
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Miller CA,
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Morris JC,
Murrell JR,
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St George-Hyslop P,
Scarpini E,
Tsuang DW,
Mancuso M,
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Wu CK,
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Nacmias B,
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Bras J,
Guerreiro R,
Al-Chalabi A,
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Sussams R,
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DeStefano AL,
Ortega-Cubero S,
Hakonarson H,
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Tzourio C,
Launer LJ,
Escott-Price V,
Mayeux R,
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Amin N,
Holmans PA,
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van Duijn CM,
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Wang LS,
Lambert JC,
Seshadri S,
Williams J,
Schellenberg GD
ARUK Consortium · GERAD/PERADES, CHARGE, ADGC, EADI
Nature genetics · 2017 · PMID 28714976
페이지 1개
Splicing variant of <i>WDFY4</i> augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis
Kochi Y,
Kamatani Y,
Kondo Y,
Suzuki A,
Kawakami E,
Hiwa R,
Momozawa Y,
Fujimoto M,
Jinnin M,
Tanaka Y,
Kanda T,
Cooper RG
외 36명 — 모두 보기
Chinoy H,
Rothwell S,
Lamb JA,
Vencovský J,
Mann H,
Ohmura K,
Myouzen K,
Ishigaki K,
Nakashima R,
Hosono Y,
Tsuboi H,
Kawasumi H,
Iwasaki Y,
Kajiyama H,
Horita T,
Ogawa-Momohara M,
Takamura A,
Tsunoda S,
Shimizu J,
Fujio K,
Amano H,
Mimori A,
Kawakami A,
Umehara H,
Takeuchi T,
Sano H,
Muro Y,
Atsumi T,
Mimura T,
Kawaguchi Y,
Mimori T,
Takahashi A,
Kubo M,
Kohsaka H,
Sumida T,
Yamamoto K
Annals of the rheumatic diseases · 2018 · PMID 29331962
페이지 1개
GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy
Hishida A,
Ugai T,
Fujii R,
Nakatochi M,
Wu MC,
Ito H,
Oze I,
Tajika M,
Niwa Y,
Nishiyama T,
Nakagawa-Senda H,
Suzuki S
외 10명 — 모두 보기
Carcinogenesis · 2019 · PMID 30753327
페이지 1개
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout
Kawamura Y,
Nakaoka H,
Nakayama A,
Okada Y,
Yamamoto K,
Higashino T,
Sakiyama M,
Shimizu T,
Ooyama H,
Ooyama K,
Nagase M,
Hidaka Y
외 38명 — 모두 보기
Shirahama Y,
Hosomichi K,
Nishida Y,
Shimoshikiryo I,
Hishida A,
Katsuura-Kamano S,
Shimizu S,
Kawaguchi M,
Uemura H,
Ibusuki R,
Hara M,
Naito M,
Takao M,
Nakajima M,
Iwasawa S,
Nakashima H,
Ohnaka K,
Nakamura T,
Stiburkova B,
Merriman TR,
Nakatochi M,
Ichihara S,
Yokota M,
Takada T,
Saitoh T,
Kamatani Y,
Takahashi A,
Arisawa K,
Takezaki T,
Tanaka K,
Wakai K,
Kubo M,
Hosoya T,
Ichida K,
Inoue I,
Shinomiya N,
Matsuo H,
Matsuo H
Annals of the rheumatic diseases · 2019 · PMID 31289104 · open access
페이지 1개
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
Yaghootkar H,
Zhang Y,
Spracklen CN,
Karaderi T,
Huang LO,
Bradfield J,
Schurmann C,
Fine RS,
Preuss MH,
Kutalik Z,
Wittemans LBL,
Lu Y
외 104명 — 모두 보기
Metz S,
Willems SM,
Li-Gao R,
Grarup N,
Wang S,
Molnos S,
Sandoval-Zárate AA,
Nalls MA,
Lange LA,
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Guo X,
Lyytikäinen LP,
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Mahajan A,
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Carrasquilla GD,
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Doege CA,
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Hakonarson H,
Hong J,
Ida Chen YD,
Jackson R,
Jakupović H,
Jousilahti P,
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Li J,
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Kilpeläinen TO
Diabetes · 2020 · PMID 32917775
페이지 1개
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene
Boer CG,
Yau MS,
Rice SJ,
Coutinho de Almeida R,
Cheung K,
Styrkarsdottir U,
Southam L,
Broer L,
Wilkinson JM,
Uitterlinden AG,
Zeggini E,
Felson D
외 5명 — 모두 보기
Annals of the rheumatic diseases · 2021 · PMID 33055079 · open access
페이지 1개
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis
Schack LMH,
Naderi E,
Fachal L,
Dorling L,
Luccarini C,
Dunning AM,
Ong EHW,
Chua MLK,
Langendijk JA,
Alizadeh BZ,
Overgaard J,
Eriksen JG
외 2명 — 모두 보기
Head and Neck Group of the Radiogenomics Consortium · Danish Head and Neck Cancer Group (DAHANCA)
British journal of cancer · 2022 · PMID 35039627 · open access
페이지 1개
Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset
Homann J,
Osburg T,
Ohlei O,
Dobricic V,
Deecke L,
Bos I,
Vandenberghe R,
Gabel S,
Scheltens P,
Teunissen CE,
Engelborghs S,
Frisoni G
외 26명 — 모두 보기
Blin O,
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Frontiers in aging neuroscience · 2022 · PMID 35386118 · open access
페이지 1개
Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement
Henkel C,
Styrkársdóttir U,
Thorleifsson G,
Stefánsdóttir L,
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Dinh KM,
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Bruun MT
외 10명 — 모두 보기
DBDS Genomic Consortium
Annals of the rheumatic diseases · 2023 · PMID 36376028
페이지 1개
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
Pan H,
Liu Z,
Ma J,
Li Y,
Zhao Y,
Zhou X,
Xiang Y,
Wang Y,
Zhou X,
He R,
Xie Y,
Zhou Q
외 48명 — 모두 보기
Yuan K,
Xu Q,
Sun Q,
Wang J,
Yan X,
Zhang H,
Wang C,
Lei L,
Liu W,
Wang X,
Ding X,
Wang T,
Xue Z,
Zhang Z,
Chen L,
Wang Q,
Liu Y,
Tang J,
Zhang X,
Peng S,
Wang C,
Ding J,
Liu C,
Wang L,
Chen H,
Shen L,
Jiang H,
Wu X,
Tan H,
Luo D,
Xiao S,
Chen X,
Tan J,
Hu Z,
Chen C,
Xia K,
Zhang Z,
Foo JN,
Blauwendraat C,
Nalls MA,
Singleton AB,
Liu J,
Chan P,
Zheng H,
Li J,
Guo J,
Yang J,
Tang B
Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)
NPJ Parkinson's disease · 2023 · PMID 36759515 · open access
페이지 1개
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왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
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.