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성함이나 학술지명, PMID로 찾아보십시오.
Ma S에 대해
78건, 그중 18건 표시.
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
Bailey JN,
Loomis SJ,
Kang JH,
Allingham RR,
Gharahkhani P,
Khor CC,
Burdon KP,
Aschard H,
Chasman DI,
Igo RP Jr,
Hysi PG,
Glastonbury CA
외 69명 — 모두 보기
Ashley-Koch A,
Brilliant M,
Brown AA,
Budenz DL,
Buil A,
Cheng CY,
Choi H,
Christen WG,
Curhan G,
De Vivo I,
Fingert JH,
Foster PJ,
Fuchs C,
Gaasterland D,
Gaasterland T,
Hewitt AW,
Hu F,
Hunter DJ,
Khawaja AP,
Lee RK,
Li Z,
Lichter PR,
Mackey DA,
McGuffin P,
Mitchell P,
Moroi SE,
Perera SA,
Pepper KW,
Qi Q,
Realini T,
Richards JE,
Ridker PM,
Rimm E,
Ritch R,
Ritchie M,
Schuman JS,
Scott WK,
Singh K,
Sit AJ,
Song YE,
Tamimi RM,
Topouzis F,
Viswanathan AC,
Verma SS,
Vollrath D,
Wang JJ,
Weisschuh N,
Wissinger B,
Wollstein G,
Wong TY,
Yaspan BL,
Zack DJ,
Zhang K,
Study EN,
Weinreb RN,
Pericak-Vance MA,
Small K,
Hammond CJ,
Aung T,
Liu Y,
Vithana EN,
MacGregor S,
Craig JE,
Kraft P,
Howell G,
Hauser MA,
Pasquale LR,
Haines JL,
Wiggs JL
ANZRAG Consortium
Nature genetics · 2016 · PMID 26752265 · open access
페이지 1개
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
van 't Hof FN,
Ruigrok YM,
Lee CH,
Ripke S,
Anderson G,
de Andrade M,
Baas AF,
Blankensteijn JD,
Böttinger EP,
Bown MJ,
Broderick J,
Bijlenga P
외 59명 — 모두 보기
Carrell DS,
Crawford DC,
Crosslin DR,
Ebeling C,
Eriksson JG,
Eriksson JG,
Fornage M,
Foroud T,
von Und Zu Fraunberg M,
Friedrich CM,
Gaál EI,
Gottesman O,
Guo DC,
Harrison SC,
Hernesniemi J,
Hofman A,
Inoue I,
Jääskeläinen JE,
Jones GT,
Kiemeney LA,
Kivisaari R,
Ko N,
Koskinen S,
Kubo M,
Kullo IJ,
Kuivaniemi H,
Kurki MI,
Laakso A,
Lai D,
Leal SM,
Lehto H,
LeMaire SA,
Low SK,
Malinowski J,
McCarty CA,
Milewicz DM,
Mosley TH,
Nakamura Y,
Nakaoka H,
Niemelä M,
Pacheco J,
Peissig PL,
Pera J,
Rasmussen-Torvik L,
Ritchie MD,
Rivadeneira F,
van Rij AM,
Santos-Cortez RL,
Saratzis A,
Slowik A,
Takahashi A,
Tromp G,
Uitterlinden AG,
Verma SS,
Vermeulen SH,
Wang GT,
Han B,
Rinkel GJ,
de Bakker PI
Aneurysm Consortium; Vascular Research Consortium of New Zealand
Journal of the American Heart Association · 2016 · PMID 27418160 · open access
페이지 1개
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Gharahkhani P,
Burdon KP,
Cooke Bailey JN,
Hewitt AW,
Law MH,
Pasquale LR,
Kang JH,
Haines JL,
Souzeau E,
Zhou T,
Siggs OM,
Landers J
외 27명 — 모두 보기
Awadalla M,
Sharma S,
Mills RA,
Ridge B,
Lynn D,
Casson R,
Graham SL,
Goldberg I,
White A,
Healey PR,
Grigg J,
Lawlor M,
Mitchell P,
Ruddle J,
Coote M,
Walland M,
Best S,
Vincent A,
Gale J,
RadfordSmith G,
Whiteman DC,
Montgomery GW,
Martin NG,
Mackey DA,
Wiggs JL,
MacGregor S,
Craig JE
NEIGHBORHOOD consortium
Scientific reports · 2018 · PMID 29449654 · open access
페이지 1개
CCDC102B confers risk of low vision and blindness in high myopia
Hosoda Y,
Yoshikawa M,
Miyake M,
Tabara Y,
Shimada N,
Zhao W,
Oishi A,
Nakanishi H,
Hata M,
Akagi T,
Ooto S,
Nagaoka N
외 8명 — 모두 보기
Nagahama Study group
Nature communications · 2018 · PMID 29725004 · open access
페이지 1개
Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility
Chen H,
Chen G,
Li G,
Zhang S,
Chen H,
Chen Y,
Duggan D,
Hu Z,
Chen J,
Zhao Y,
Zhao Y,
Huang H
외 11명 — 모두 보기
Zheng SL,
Trent JM,
Yu L,
Jiang D,
Mo Z,
Wang H,
Mou Y,
Jiang T,
Mao Y,
Xu J,
Lu D
International journal of cancer · 2019 · PMID 30714141
페이지 1개
Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL,
Graff M,
Nishimura KK,
Tao R,
Haessler J,
Gignoux CR,
Highland HM,
Patel YM,
Sorokin EP,
Avery CL,
Belbin GM,
Bien SA
외 74명 — 모두 보기
Cheng I,
Cullina S,
Hodonsky CJ,
Hu Y,
Huckins LM,
Jeff J,
Justice AE,
Kocarnik JM,
Lim U,
Lin BM,
Lu Y,
Nelson SC,
Park SL,
Poisner H,
Preuss MH,
Richard MA,
Schurmann C,
Setiawan VW,
Sockell A,
Vahi K,
Verbanck M,
Vishnu A,
Walker RW,
Young KL,
Zubair N,
Acuña-Alonso V,
Ambite JL,
Barnes KC,
Boerwinkle E,
Bottinger EP,
Bustamante CD,
Caberto C,
Canizales-Quinteros S,
Conomos MP,
Deelman E,
Do R,
Doheny K,
Fernández-Rhodes L,
Fornage M,
Hailu B,
Heiss G,
Henn BM,
Hindorff LA,
Jackson RD,
Laurie CA,
Laurie CC,
Li Y,
Lin DY,
Moreno-Estrada A,
Nadkarni G,
Norman PJ,
Pooler LC,
Reiner AP,
Romm J,
Sabatti C,
Sandoval K,
Sheng X,
Stahl EA,
Stram DO,
Thornton TA,
Wassel CL,
Wilkens LR,
Winkler CA,
Yoneyama S,
Buyske S,
Haiman CA,
Kooperberg C,
Le Marchand L,
Loos RJF,
Matise TC,
North KE,
Peters U,
Kenny EE,
Carlson CS
Nature · 2019 · PMID 31217584
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
Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes
Din L,
Sheikh M,
Kosaraju N,
Smedby KE,
Bernatsky S,
Berndt SI,
Skibola CF,
Nieters A,
Wang S,
McKay JD,
Cocco P,
Maynadié M
외 80명 — 모두 보기
Foretová L,
Staines A,
Mack TM,
de Sanjosé S,
Vyse TJ,
Padyukov L,
Monnereau A,
Arslan AA,
Moore A,
Brooks-Wilson AR,
Novak AJ,
Glimelius B,
Birmann BM,
Link BK,
Stewart C,
Vajdic CM,
Haioun C,
Magnani C,
Conti DV,
Cox DG,
Casabonne D,
Albanes D,
Kane E,
Roman E,
Muzi G,
Salles G,
Giles GG,
Adami HO,
Ghesquières H,
De Vivo I,
Clavel J,
Cerhan JR,
Spinelli JJ,
Hofmann J,
Vijai J,
Curtin K,
Costenbader KH,
Onel K,
Offit K,
Teras LR,
Morton L,
Conde L,
Miligi L,
Melbye M,
Ennas MG,
Liebow M,
Purdue MP,
Glenn M,
Southey MC,
Din M,
Rothman N,
Camp NJ,
Wong Doo N,
Becker N,
Pradhan N,
Bracci PM,
Boffetta P,
Vineis P,
Brennan P,
Kraft P,
Lan Q,
Severson RK,
Vermeulen RCH,
Milne RL,
Kaaks R,
Travis RC,
Weinstein SJ,
Chanock SJ,
Ansell SM,
Slager SL,
Zheng T,
Zhang Y,
Benavente Y,
Taub Z,
Madireddy L,
Gourraud PA,
Oksenberg JR,
Cozen W,
Hjalgrim H,
Khankhanian P
Genetic epidemiology · 2019 · PMID 31407831
페이지 1개
An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer
Oh JJ,
Shivakumar M,
Miller J,
Verma S,
Lee H,
Hong SK,
Lee SE,
Lee Y,
Lee SJ,
Sung J,
Kim D,
Byun SS
Scientific reports · 2019 · PMID 31748686 · open access
페이지 1개
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy
Hosoda Y,
Miyake M,
Schellevis RL,
Boon CJF,
Hoyng CB,
Miki A,
Meguro A,
Sakurada Y,
Yoneyama S,
Takasago Y,
Hata M,
Muraoka Y
외 22명 — 모두 보기
Nakanishi H,
Oishi A,
Ooto S,
Tamura H,
Uji A,
Miyata M,
Takahashi A,
Ueda-Arakawa N,
Tajima A,
Sato T,
Mizuki N,
Shiragami C,
Iida T,
Khor CC,
Wong TY,
Yamada R,
Honda S,
de Jong EK,
Hollander AID,
Matsuda F,
Yamashiro K,
Tsujikawa A
Communications biology · 2019 · PMID 31872073 · open access
페이지 1개
Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium
Verma SS,
Bergmeijer TO,
Gong L,
Reny JL,
Lewis JP,
Mitchell BD,
Alexopoulos D,
Aradi D,
Altman RB,
Bliden K,
Bradford Y,
Campo G
외 36명 — 모두 보기
Chang K,
Cleator JH,
Déry JP,
Dridi NP,
Fernandez-Cadenas I,
Fontana P,
Gawaz M,
Geisler T,
Gensini GF,
Giusti B,
Gurbel PA,
Hochholzer W,
Holmvang L,
Kim EY,
Kim HS,
Marcucci R,
Montaner J,
Backman JD,
Pakyz RE,
Roden DM,
Schaeffeler E,
Schwab M,
Shin JG,
Siller-Matula JM,
Ten Berg JM,
Trenk D,
Valgimigli M,
Wallace J,
Wen MS,
Kubo M,
Lee MTM,
Whaley R,
Winter S,
Klein TE,
Shuldiner AR,
Ritchie MD
ICPC Investigators
Clinical pharmacology and therapeutics · 2020 · PMID 32472697
페이지 1개
Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator
Yamada M,
Motoike IN,
Kojima K,
Fuse N,
Hozawa A,
Kuriyama S,
Katsuoka F,
Tadaka S,
Shirota M,
Sakurai M,
Nakamura T,
Hamanaka Y
외 14명 — 모두 보기
Suzuki K,
Sugawara J,
Ogishima S,
Uruno A,
Kodama EN,
Fujino N,
Numakura T,
Ichikawa T,
Mitsune A,
Ohe T,
Kinoshita K,
Ichinose M,
Sugiura H,
Yamamoto M
Communications biology · 2021 · PMID 34782693 · open access
페이지 1개
Longitudinal lung function and gas transfer in individuals with idiopathic pulmonary fibrosis: a genome-wide association study
Allen RJ,
Oldham JM,
Jenkins DA,
Leavy OC,
Guillen-Guio B,
Melbourne CA,
Ma SF,
Jou J,
Kim JS,
Fahy WA,
Oballa E,
Hubbard RB
외 19명 — 모두 보기
Navaratnam V,
Braybrooke R,
Saini G,
Roach KM,
Tobin MD,
Hirani N,
Whyte MKB,
Kaminski N,
Zhang Y,
Martinez FJ,
Linderholm AL,
Adegunsoye A,
Strek ME,
Maher TM,
Molyneaux PL,
Flores C,
Noth I,
Gisli Jenkins R,
Wain LV
CleanUP-IPF Investigators of the Pulmonary Trials Cooperative
The Lancet. Respiratory medicine · 2023 · PMID 35985358 · open access
페이지 1개
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
외 128명 — 모두 보기
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
페이지 1개
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
Williamson A,
Norris DM,
Yin X,
Broadaway KA,
Moxley AH,
Vadlamudi S,
Wilson EP,
Jackson AU,
Ahuja V,
Andersen MK,
Arzumanyan Z,
Bonnycastle LL
외 103명 — 모두 보기
Bornstein SR,
Bretschneider MP,
Buchanan TA,
Chang YC,
Chuang LM,
Chung RH,
Clausen TD,
Damm P,
Delgado GE,
de Mello VD,
Dupuis J,
Dwivedi OP,
Erdos MR,
Fernandes Silva L,
Frayling TM,
Gieger C,
Goodarzi MO,
Guo X,
Gustafsson S,
Hakaste L,
Hammar U,
Hatem G,
Herrmann S,
Højlund K,
Horn K,
Hsueh WA,
Hung YJ,
Hwu CM,
Jonsson A,
Kårhus LL,
Kleber ME,
Kovacs P,
Lakka TA,
Lauzon M,
Lee IT,
Lindgren CM,
Lindström J,
Linneberg A,
Liu CT,
Luan J,
Aly DM,
Mathiesen E,
Moissl AP,
Morris AP,
Narisu N,
Perakakis N,
Peters A,
Prasad RB,
Rodionov RN,
Roll K,
Rundsten CF,
Sarnowski C,
Savonen K,
Scholz M,
Sharma S,
Stinson SE,
Suleman S,
Tan J,
Taylor KD,
Uusitupa M,
Vistisen D,
Witte DR,
Walther R,
Wu P,
Xiang AH,
Zethelius B,
Ahlqvist E,
Bergman RN,
Chen YI,
Collins FS,
Fall T,
Florez JC,
Fritsche A,
Grallert H,
Groop L,
Hansen T,
Koistinen HA,
Komulainen P,
Laakso M,
Lind L,
Loeffler M,
März W,
Meigs JB,
Raffel LJ,
Rauramaa R,
Rotter JI,
Schwarz PEH,
Stumvoll M,
Sundström J,
Tönjes A,
Tuomi T,
Tuomilehto J,
Wagner R,
Barroso I,
Walker M,
Grarup N,
Boehnke M,
Wareham NJ,
Mohlke KL,
Wheeler E,
O'Rahilly S,
Fazakerley DJ,
Langenberg C
Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37291194 · open access
페이지 1개
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity
Rämö JT,
Kany S,
Hou CR,
Friedman SF,
Roselli C,
Nauffal V,
Koyama S,
Karjalainen J,
Maddah M,
Palotie A,
Ellinor PT,
Pirruccello JP
FinnGen
JAMA cardiology · 2024 · PMID 38477908
페이지 1개
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer
Sun X,
Verma SP,
Jia G,
Wang X,
Ping J,
Guo X,
Shu XO,
Chen J,
Derkach A,
Cai Q,
Liang X,
Long J
외 34명 — 모두 보기
Offit K,
Oh JH,
Reiner AS,
Watt GP,
Woods M,
Yang Y,
Ambrosone CB,
Ambs S,
Chen Y,
Concannon P,
Garcia-Closas M,
Gu J,
Haiman CA,
Hu JJ,
Huo D,
John EM,
Knight JA,
Li CI,
Lynch CF,
Mellemkjær L,
Nathanson KL,
Nemesure B,
Olopade OI,
Olshan AF,
Pal T,
Palmer JR,
Press MF,
Sanderson M,
Sandler DP,
Troester MA,
Zheng W,
Bernstein JL,
Buas MF,
Shu X
Cancer research · 2024 · PMID 38832928
페이지 1개
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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.