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The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition
van der Meer D,
Gurholt TP,
Sønderby IE,
Shadrin AA,
Hindley G,
Rahman Z,
de Lange AG,
Frei O,
Leinhard OD,
Linge J,
Simon R,
Beck D
외 6명 — 모두 보기
Communications biology · 2022 · PMID 36402844 · open access
페이지 10개
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Phelan CM,
Kuchenbaecker KB,
Tyrer JP,
Kar SP,
Lawrenson K,
Winham SJ,
Dennis J,
Pirie A,
Riggan MJ,
Chornokur G,
Earp MA,
Lyra PC Jr
외 402명 — 모두 보기
Lee JM,
Coetzee S,
Beesley J,
McGuffog L,
Soucy P,
Dicks E,
Lee A,
Barrowdale D,
Lecarpentier J,
Leslie G,
Aalfs CM,
Aben KKH,
Adams M,
Adlard J,
Andrulis IL,
Anton-Culver H,
Antonenkova N,
Aravantinos G,
Arnold N,
Arun BK,
Arver B,
Azzollini J,
Balmaña J,
Banerjee SN,
Barjhoux L,
Barkardottir RB,
Bean Y,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bermisheva M,
Bernardini MQ,
Birrer MJ,
Bjorge L,
Black A,
Blankstein K,
Blok MJ,
Bodelon C,
Bogdanova N,
Bojesen A,
Bonanni B,
Borg Å,
Bradbury AR,
Brenton JD,
Brewer C,
Brinton L,
Broberg P,
Brooks-Wilson A,
Bruinsma F,
Brunet J,
Buecher B,
Butzow R,
Buys SS,
Caldes T,
Caligo MA,
Campbell I,
Cannioto R,
Carney ME,
Cescon T,
Chan SB,
Chang-Claude J,
Chanock S,
Chen XQ,
Chiew YE,
Chiquette J,
Chung WK,
Claes KBM,
Conner T,
Cook LS,
Cook J,
Cramer DW,
Cunningham JM,
D'Aloisio AA,
Daly MB,
Damiola F,
Damirovna SD,
Dansonka-Mieszkowska A,
Dao F,
Davidson R,
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Delnatte C,
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Diez O,
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Domchek SM,
Dorfling CM,
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Hansen TVO,
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Luccarini C,
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Massuger LFAG,
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McAlpine JN,
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McNeish I,
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Side LE,
Sieh W,
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Sukiennicki G,
Sutphen R,
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Swerdlow AJ,
Szabo CI,
Szafron L,
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Taylor JA,
Tea MK,
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Teo SH,
Terry KL,
Thompson PJ,
Thomsen LCV,
Thull DL,
Tihomirova L,
Tinker AV,
Tischkowitz M,
Tognazzo S,
Toland AE,
Tone A,
Trabert B,
Travis RC,
Trichopoulou A,
Tung N,
Tworoger SS,
van Altena AM,
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van der Hout AH,
van der Luijt RB,
Van Heetvelde M,
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van Rensburg EJ,
Vanderstichele A,
Varon-Mateeva R,
Vega A,
Edwards DV,
Vergote I,
Vierkant RA,
Vijai J,
Vratimos A,
Walker L,
Walsh C,
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Wappenschmidt B,
Webb PM,
Weinberg CR,
Weitzel JN,
Wentzensen N,
Whittemore AS,
Wijnen JT,
Wilkens LR,
Wolk A,
Woo M,
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Wu AH,
Yang H,
Yannoukakos D,
Ziogas A,
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Easton DF,
Amos CI,
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AOCS study group · EMBRACE Study 외 컨소시엄 4곳
Nature genetics · 2017 · PMID 28346442
페이지 9개
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
Bjornsdottir G,
Stefansdottir L,
Thorleifsson G,
Sulem P,
Norland K,
Ferkingstad E,
Oddsson A,
Zink F,
Lund SH,
Nawaz MS,
Bragi Walters G,
Skuladottir AT
외 32명 — 모두 보기
Gudjonsson SA,
Einarsson G,
Halldorsson GH,
Bjarnadottir V,
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Helgadottir A,
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Gudbjartsson DF,
Thorgeirsson TE,
Stefansson K
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
페이지 9개
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
외 391명 — 모두 보기
Damotte V,
van der Lee SJ,
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Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
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EADB · GR@ACE 외 컨소시엄 7곳
Nature genetics · 2022 · PMID 35379992 · open access
페이지 9개
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
외 121명 — 모두 보기
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
Sliz E,
Sobalska-Kwapis M,
Thorleifsson G,
Topbas-Selcuki NF,
Vitonis A,
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Arnadottir R,
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Campbell A,
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Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study 외 컨소시엄 3곳
Nature genetics · 2023 · PMID 36914876
페이지 8개
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Eeles RA,
Olama AA,
Benlloch S,
Saunders EJ,
Leongamornlert DA,
Tymrakiewicz M,
Ghoussaini M,
Luccarini C,
Dennis J,
Jugurnauth-Little S,
Dadaev T,
Neal DE
외 132명 — 모두 보기
Hamdy FC,
Donovan JL,
Muir K,
Giles GG,
Severi G,
Wiklund F,
Gronberg H,
Haiman CA,
Schumacher F,
Henderson BE,
Le Marchand L,
Lindstrom S,
Kraft P,
Hunter DJ,
Gapstur S,
Chanock SJ,
Berndt SI,
Albanes D,
Andriole G,
Schleutker J,
Weischer M,
Canzian F,
Riboli E,
Key TJ,
Travis RC,
Campa D,
Ingles SA,
John EM,
Hayes RB,
Pharoah PD,
Pashayan N,
Khaw KT,
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Nature genetics · 2013 · PMID 23535732
페이지 7개
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외 164명 — 모두 보기
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Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
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페이지 7개
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
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외 4명 — 모두 보기
HCMR Investigators
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페이지 7개
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외 1명 — 모두 보기
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페이지 7개
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외 212명 — 모두 보기
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페이지 6개
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ExomeBP Consortium · MAGIC Consortium 외 컨소시엄 1곳
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페이지 6개
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
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외 32명 — 모두 보기
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페이지 6개
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외 25명 — 모두 보기
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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.