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성함이나 학술지명, PMID로 찾아보십시오.
van Rooij FJ에 대해
19건.
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Ganesh SK,
Zakai NA,
van Rooij FJ,
Soranzo N,
Smith AV,
Nalls MA,
Chen MH,
Kottgen A,
Glazer NL,
Dehghan A,
Kuhnel B,
Aspelund T
외 50명 — 모두 보기
Yang Q,
Tanaka T,
Jaffe A,
Bis JC,
Verwoert GC,
Teumer A,
Fox CS,
Guralnik JM,
Ehret GB,
Rice K,
Felix JF,
Rendon A,
Eiriksdottir G,
Levy D,
Patel KV,
Boerwinkle E,
Rotter JI,
Hofman A,
Sambrook JG,
Hernandez DG,
Zheng G,
Bandinelli S,
Singleton AB,
Coresh J,
Lumley T,
Uitterlinden AG,
Vangils JM,
Launer LJ,
Cupples LA,
Oostra BA,
Zwaginga JJ,
Ouwehand WH,
Thein SL,
Meisinger C,
Deloukas P,
Nauck M,
Spector TD,
Gieger C,
Gudnason V,
van Duijn CM,
Psaty BM,
Ferrucci L,
Chakravarti A,
Greinacher A,
O'Donnell CJ,
Witteman JC,
Furth S,
Cushman M,
Harris TB,
Lin JP
Nature genetics · 2009 · PMID 19862010 · open access
페이지 12개+
Genome-wide association study identifies 74 loci associated with educational attainment
Okbay A,
Beauchamp JP,
Fontana MA,
Lee JJ,
Pers TH,
Rietveld CA,
Turley P,
Chen GB,
Emilsson V,
Meddens SF,
Oskarsson S,
Pickrell JK
외 243명 — 모두 보기
Thom K,
Timshel P,
de Vlaming R,
Abdellaoui A,
Ahluwalia TS,
Bacelis J,
Baumbach C,
Bjornsdottir G,
Brandsma JH,
Pina Concas M,
Derringer J,
Furlotte NA,
Galesloot TE,
Girotto G,
Gupta R,
Hall LM,
Harris SE,
Hofer E,
Horikoshi M,
Huffman JE,
Kaasik K,
Kalafati IP,
Karlsson R,
Kong A,
Lahti J,
van der Lee SJ,
deLeeuw C,
Lind PA,
Lindgren KO,
Liu T,
Mangino M,
Marten J,
Mihailov E,
Miller MB,
van der Most PJ,
Oldmeadow C,
Payton A,
Pervjakova N,
Peyrot WJ,
Qian Y,
Raitakari O,
Rueedi R,
Salvi E,
Schmidt B,
Schraut KE,
Shi J,
Smith AV,
Poot RA,
St Pourcain B,
Teumer A,
Thorleifsson G,
Verweij N,
Vuckovic D,
Wellmann J,
Westra HJ,
Yang J,
Zhao W,
Zhu Z,
Alizadeh BZ,
Amin N,
Bakshi A,
Baumeister SE,
Biino G,
Bønnelykke K,
Boyle PA,
Campbell H,
Cappuccio FP,
Davies G,
De Neve JE,
Deloukas P,
Demuth I,
Ding J,
Eibich P,
Eisele L,
Eklund N,
Evans DM,
Faul JD,
Feitosa MF,
Forstner AJ,
Gandin I,
Gunnarsson B,
Halldórsson BV,
Harris TB,
Heath AC,
Hocking LJ,
Holliday EG,
Homuth G,
Horan MA,
Hottenga JJ,
de Jager PL,
Joshi PK,
Jugessur A,
Kaakinen MA,
Kähönen M,
Kanoni S,
Keltigangas-Järvinen L,
Kiemeney LA,
Kolcic I,
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Kraja AT,
Kroh M,
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Latvala A,
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Lebreton MP,
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Palotie A,
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Porteous DJ,
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Rudan I,
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Salomaa V,
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Schmidt H,
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Staessen JA,
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Terracciano A,
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Venturini C,
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Chabris CF,
Cucca F,
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van Duijn CM,
Eriksson JG,
Franke B,
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LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
페이지 12개+
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
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Feenstra B,
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외 157명 — 모두 보기
Li-Gao R,
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Wang X,
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CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
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,
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Zhong X
외 98명 — 모두 보기
Manansala R,
Laplante V,
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Lo KS,
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Beaudoin M,
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Manichaikul A,
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Wilson PWF,
Li Y,
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Okada Y,
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Johnson AD,
Reiner AP,
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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,
Megy K
외 100명 — 모두 보기
Ponstingl H,
Penkett CJ,
Albers PK,
Wigdor EM,
Sakaue S,
Moscati A,
Manansala R,
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Chitrala KN,
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Karthikeyan S,
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Lange LA,
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Linneberg A,
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Manichaikul A,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
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Pankratz N,
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Preuss M,
Psaty BM,
Raitakari OT,
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Rodriguez BAT,
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Surendran P,
Tang H,
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Johnson AD,
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Ouwehand WH,
Lettre G,
Sankaran VG,
Soranzo N
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
페이지 12개+
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Wang Z,
Emmerich A,
Pillon NJ,
Moore T,
Hemerich D,
Cornelis MC,
Mazzaferro E,
Broos S,
Ahluwalia TS,
Bartz TM,
Bentley AR,
Bielak LF
외 206명 — 모두 보기
Chong M,
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Berry D,
Dorajoo R,
Dueker ND,
Kasbohm E,
Feenstra B,
Feitosa MF,
Gieger C,
Graff M,
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Jackson AU,
Johansson Å,
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Kaakinen MA,
Karlsson R,
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Lagou V,
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Lyytikäinen LP,
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Pacolet A,
Pérusse L,
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Rivera NV,
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van der Most PJ,
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Zhang X,
Zhao JH,
Zhao W,
Balkhiyarova Z,
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Beilby J,
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Boomsma DI,
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Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
페이지 12개+
Genome-wide association study identifies 48 common genetic variants associated with handedness
Cuellar-Partida G,
Tung JY,
Eriksson N,
Albrecht E,
Aliev F,
Andreassen OA,
Barroso I,
Beckmann JS,
Boks MP,
Boomsma DI,
Boyd HA,
Breteler MMB
외 106명 — 모두 보기
Campbell H,
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Davies G,
de Geus EJC,
Deary IJ,
Deloukas P,
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Nature human behaviour · 2021 · PMID 32989287
페이지 6개
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
Okada Y,
Hirota T,
Kamatani Y,
Takahashi A,
Ohmiya H,
Kumasaka N,
Higasa K,
Yamaguchi-Kabata Y,
Hosono N,
Nalls MA,
Chen MH,
van Rooij FJ
외 19명 — 모두 보기
Smith AV,
Tanaka T,
Couper DJ,
Zakai NA,
Ferrucci L,
Longo DL,
Hernandez DG,
Witteman JC,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Tamari M,
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외 88명 — 모두 보기
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외 89명 — 모두 보기
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외 24명 — 모두 보기
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Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) 외 컨소시엄 2곳
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Common genetic variants associate with serum phosphorus concentration
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외 27명 — 모두 보기
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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.