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성함이나 학술지명, PMID로 찾아보십시오.
Whiteman DC에 대해
19건.
Combined analysis of keratinocyte cancers identifies novel genome-wide loci
Liyanage UE,
Law MH,
Han X,
An J,
Ong JS,
Gharahkhani P,
Gordon S,
Neale RE,
Olsen CM,
MacGregor S,
Whiteman DC
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
페이지 12개+
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Landi MT,
Bishop DT,
MacGregor S,
Machiela MJ,
Stratigos AJ,
Ghiorzo P,
Brossard M,
Calista D,
Choi J,
Fargnoli MC,
Zhang T,
Rodolfo M
외 140명 — 모두 보기
Trower AJ,
Menin C,
Martinez J,
Hadjisavvas A,
Song L,
Stefanaki I,
Scolyer R,
Yang R,
Goldstein AM,
Potrony M,
Kypreou KP,
Pastorino L,
Queirolo P,
Pellegrini C,
Cattaneo L,
Zawistowski M,
Gimenez-Xavier P,
Rodriguez A,
Elefanti L,
Manoukian S,
Rivoltini L,
Smith BH,
Loizidou MA,
Del Regno L,
Massi D,
Mandala M,
Khosrotehrani K,
Akslen LA,
Amos CI,
Andresen PA,
Avril MF,
Azizi E,
Soyer HP,
Bataille V,
Dalmasso B,
Bowdler LM,
Burdon KP,
Chen WV,
Codd V,
Craig JE,
Dębniak T,
Falchi M,
Fang S,
Friedman E,
Simi S,
Galan P,
Garcia-Casado Z,
Gillanders EM,
Gordon S,
Green A,
Gruis NA,
Hansson J,
Harland M,
Harris J,
Helsing P,
Henders A,
Hočevar M,
Höiom V,
Hunter D,
Ingvar C,
Kumar R,
Lang J,
Lathrop GM,
Lee JE,
Li X,
Lubiński J,
Mackie RM,
Malt M,
Malvehy J,
McAloney K,
Mohamdi H,
Molven A,
Moses EK,
Neale RE,
Novaković S,
Nyholt DR,
Olsson H,
Orr N,
Fritsche LG,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
Randerson-Moor J,
Requena C,
Rowe C,
Samani NJ,
Sanna M,
Schadendorf D,
Schulze HJ,
Simms LA,
Smithers M,
Song F,
Swerdlow AJ,
van der Stoep N,
Kukutsch NA,
Visconti A,
Wallace L,
Ward SV,
Wheeler L,
Sturm RA,
Hutchinson A,
Jones K,
Malasky M,
Vogt A,
Zhou W,
Pooley KA,
Elder DE,
Han J,
Hicks B,
Hayward NK,
Kanetsky PA,
Brummett C,
Montgomery GW,
Olsen CM,
Hayward C,
Dunning AM,
Martin NG,
Evangelou E,
Mann GJ,
Long G,
Pharoah PDP,
Easton DF,
Barrett JH,
Cust AE,
Abecasis G,
Duffy DL,
Whiteman DC,
Gogas H,
De Nicolo A,
Tucker MA,
Newton-Bishop JA,
Peris K,
Chanock SJ,
Demenais F,
Brown KM,
Puig S,
Nagore E,
Shi J,
Iles MM,
Law MH
GenoMEL Consortium · Q-MEGA and QTWIN Investigators 외 컨소시엄 7곳
Nature genetics · 2020 · PMID 32341527 · open access
페이지 12개+
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Zhou W,
Kanai M,
Wu KH,
Rasheed H,
Tsuo K,
Hirbo JB,
Wang Y,
Bhattacharya A,
Zhao H,
Namba S,
Surakka I,
Wolford BN
외 140명 — 모두 보기
Lo Faro V,
Lopera-Maya EA,
Läll K,
Favé MJ,
Partanen JJ,
Chapman SB,
Karjalainen J,
Kurki M,
Maasha M,
Brumpton BM,
Chavan S,
Chen TT,
Daya M,
Ding Y,
Feng YA,
Guare LA,
Gignoux CR,
Graham SE,
Hornsby WE,
Ingold N,
Ismail SI,
Johnson R,
Laisk T,
Lin K,
Lv J,
Millwood IY,
Moreno-Grau S,
Nam K,
Palta P,
Pandit A,
Preuss MH,
Saad C,
Setia-Verma S,
Thorsteinsdottir U,
Uzunovic J,
Verma A,
Zawistowski M,
Zhong X,
Afifi N,
Al-Dabhani KM,
Al Thani A,
Bradford Y,
Campbell A,
Crooks K,
de Bock GH,
Damrauer SM,
Douville NJ,
Finer S,
Fritsche LG,
Fthenou E,
Gonzalez-Arroyo G,
Griffiths CJ,
Guo Y,
Hunt KA,
Ioannidis A,
Jansonius NM,
Konuma T,
Lee MTM,
Lopez-Pineda A,
Matsuda Y,
Marioni RE,
Moatamed B,
Nava-Aguilar MA,
Numakura K,
Patil S,
Rafaels N,
Richmond A,
Rojas-Muñoz A,
Shortt JA,
Straub P,
Tao R,
Vanderwerff B,
Vernekar M,
Veturi Y,
Barnes KC,
Boezen M,
Chen Z,
Chen CY,
Cho J,
Smith GD,
Finucane HK,
Franke L,
Gamazon ER,
Ganna A,
Gaunt TR,
Ge T,
Huang H,
Huffman J,
Katsanis N,
Koskela JT,
Lajonchere C,
Law MH,
Li L,
Lindgren CM,
Loos RJF,
MacGregor S,
Matsuda K,
Olsen CM,
Porteous DJ,
Shavit JA,
Snieder H,
Takano T,
Trembath RC,
Vonk JM,
Whiteman DC,
Wicks SJ,
Wijmenga C,
Wright J,
Zheng J,
Zhou X,
Awadalla P,
Boehnke M,
Bustamante CD,
Cox NJ,
Fatumo S,
Geschwind DH,
Hayward C,
Hveem K,
Kenny EE,
Lee S,
Lin YF,
Mbarek H,
Mägi R,
Martin HC,
Medland SE,
Okada Y,
Palotie AV,
Pasaniuc B,
Rader DJ,
Ritchie MD,
Sanna S,
Smoller JW,
Stefansson K,
van Heel DA,
Walters RG,
Zöllner S,
Martin AR,
Willer CJ,
Daly MJ,
Neale BM
Biobank of the Americas · Biobank Japan Project 외 컨소시엄 22곳
Cell genomics · 2022 · PMID 36777996 · open access
페이지 12개+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
외 73명 — 모두 보기
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium 외 컨소시엄 4곳
Nature genetics · 2026 · PMID 41644669 · open access
페이지 12개+
Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma
MacGregor S,
Ong JS,
An J,
Han X,
Zhou T,
Siggs OM,
Law MH,
Souzeau E,
Sharma S,
Lynn DJ,
Beesley J,
Sheldrick B
외 20명 — 모두 보기
Mills RA,
Landers J,
Ruddle JB,
Graham SL,
Healey PR,
White AJR,
Casson RJ,
Best S,
Grigg JR,
Goldberg I,
Powell JE,
Whiteman DC,
Radford-Smith GL,
Martin NG,
Montgomery GW,
Burdon KP,
Mackey DA,
Gharahkhani P,
Craig JE,
Hewitt AW
Nature genetics · 2018 · PMID 30054594
페이지 10개
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,
Westergaard D,
Arnadottir R,
Burgdorf KS,
Campbell A,
Cheuk CSK,
Clementi C,
Cook J,
De Vivo I,
DiVasta A,
Dorien O,
Donoghue JF,
Edwards T,
Fontanillas P,
Fung JN,
Geirsson RT,
Girling JE,
Harkki P,
Harris HR,
Healey M,
Heikinheimo O,
Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
Jarvelin MR,
Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
Laivuori H,
Laufer MR,
Lindgren CM,
MacGregor S,
Mangino M,
Martin NG,
Matalliotaki C,
Matalliotakis M,
Murray AD,
Ndungu A,
Nezhat C,
Olsen CM,
Opoku-Anane J,
Padmanabhan S,
Paranjpe M,
Peters M,
Polak G,
Porteous DJ,
Rabban J,
Rexrode KM,
Romanowicz H,
Saare M,
Saavalainen L,
Schork AJ,
Sen S,
Shafrir AL,
Siewierska-Górska A,
Słomka M,
Smith BH,
Smolarz B,
Szaflik T,
Szyłło K,
Takahashi A,
Terry KL,
Tomassetti C,
Treloar SA,
Vanhie A,
Vincent K,
Vo KC,
Werring DJ,
Zeggini E,
Zervou MI,
Adachi S,
Buring JE,
Ridker PM,
D'Hooghe T,
Goulielmos GN,
Hapangama DK,
Hayward C,
Horne AW,
Low SK,
Martikainen H,
Chasman DI,
Rogers PAW,
Saunders PT,
Sirota M,
Spector T,
Strapagiel D,
Tung JY,
Whiteman DC,
Giudice LC,
Velez-Edwards DR,
Uimari O,
Kraft P,
Salumets A,
Nyholt DR,
Mägi R,
Stefansson K,
Becker CM,
Yurttas-Beim P,
Steinthorsdottir V,
Nyegaard M,
Missmer SA,
Montgomery GW,
Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study 외 컨소시엄 3곳
Nature genetics · 2023 · PMID 36914876
페이지 8개
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis
Gharahkhani P,
Fitzgerald RC,
Vaughan TL,
Palles C,
Gockel I,
Tomlinson I,
Buas MF,
May A,
Gerges C,
Anders M,
Becker J,
Kreuser N
외 57명 — 모두 보기
Noder T,
Venerito M,
Veits L,
Schmidt T,
Manner H,
Schmidt C,
Hess T,
Böhmer AC,
Izbicki JR,
Hölscher AH,
Lang H,
Lorenz D,
Schumacher B,
Hackelsberger A,
Mayershofer R,
Pech O,
Vashist Y,
Ott K,
Vieth M,
Weismüller J,
Nöthen MM,
Attwood S,
Barr H,
Chegwidden L,
de Caestecker J,
Harrison R,
Love SB,
MacDonald D,
Moayyedi P,
Prenen H,
Watson RGP,
Iyer PG,
Anderson LA,
Bernstein L,
Chow WH,
Hardie LJ,
Lagergren J,
Liu G,
Risch HA,
Wu AH,
Ye W,
Bird NC,
Shaheen NJ,
Gammon MD,
Corley DA,
Caldas C,
Moebus S,
Knapp M,
Peters WHM,
Neuhaus H,
Rösch T,
Ell C,
MacGregor S,
Pharoah P,
Whiteman DC,
Jankowski J,
Schumacher J
Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) · Esophageal Adenocarcinoma GenEtics Consortium (EAGLE) 외 컨소시엄 1곳
The Lancet. Oncology · 2016 · PMID 27527254 · open access
페이지 6개
Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma
Liyanage UE,
MacGregor S,
Bishop DT,
Shi J,
An J,
Ong JS,
Han X,
Scolyer RA,
Martin NG,
Medland SE,
Byrne EM,
Green AC
외 14명 — 모두 보기
Saw RPM,
Thompson JF,
Stretch J,
Spillane A,
Jiang Y,
Tian C,
Gordon SG,
Duffy DL,
Olsen CM,
Whiteman DC,
Long GV,
Iles MM,
Landi MT,
Law MH
23andMe Research Team
The Journal of investigative dermatology · 2022 · PMID 34813871
페이지 5개
Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases
An J,
Gharahkhani P,
Law MH,
Ong JS,
Han X,
Olsen CM,
Neale RE,
Lai J,
Vaughan TL,
Gockel I,
Thieme R,
Böhmer AC
외 6명 — 모두 보기
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
페이지 4개
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma
Gharahkhani P,
Burdon KP,
Fogarty R,
Sharma S,
Hewitt AW,
Martin S,
Law MH,
Cremin K,
Bailey JNC,
Loomis SJ,
Pasquale LR,
Haines JL
외 30명 — 모두 보기
Hauser MA,
Viswanathan AC,
McGuffin P,
Topouzis F,
Foster PJ,
Graham SL,
Casson RJ,
Chehade M,
White AJ,
Zhou T,
Souzeau E,
Landers J,
Fitzgerald JT,
Klebe S,
Ruddle JB,
Goldberg I,
Healey PR,
Mills RA,
Wang JJ,
Montgomery GW,
Martin NG,
RadfordSmith G,
Whiteman DC,
Brown MA,
Brown MA,
Wiggs JL,
Mackey DA,
Mitchell P,
MacGregor S,
Craig JE
Wellcome Trust Case Control Consortium 2, NEIGHBORHOOD consortium
Nature genetics · 2014 · PMID 25173105 · open access
페이지 3개
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
외 180명 — 모두 보기
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium 외 컨소시엄 2곳
Nature genetics · 2021 · PMID 34873335 · open access
페이지 3개
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Law MH,
Bishop DT,
Lee JE,
Brossard M,
Martin NG,
Moses EK,
Song F,
Barrett JH,
Kumar R,
Easton DF,
Pharoah PDP,
Swerdlow AJ
외 63명 — 모두 보기
Kypreou KP,
Taylor JC,
Harland M,
Randerson-Moor J,
Akslen LA,
Andresen PA,
Avril MF,
Azizi E,
Scarrà GB,
Brown KM,
Dębniak T,
Duffy DL,
Elder DE,
Fang S,
Friedman E,
Galan P,
Ghiorzo P,
Gillanders EM,
Goldstein AM,
Gruis NA,
Hansson J,
Helsing P,
Hočevar M,
Höiom V,
Ingvar C,
Kanetsky PA,
Chen WV,
Landi MT,
Lang J,
Lathrop GM,
Lubiński J,
Mackie RM,
Mann GJ,
Molven A,
Montgomery GW,
Novaković S,
Olsson H,
Puig S,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
van der Stoep N,
van Doorn R,
Whiteman DC,
Craig JE,
Schadendorf D,
Simms LA,
Burdon KP,
Nyholt DR,
Pooley KA,
Orr N,
Stratigos AJ,
Cust AE,
Ward SV,
Hayward NK,
Han J,
Schulze HJ,
Dunning AM,
Bishop JAN,
Demenais F,
Amos CI,
MacGregor S,
Iles MM
GenoMEL Consortium · Essen-Heidelberg Investigators 외 컨소시엄 4곳
Nature genetics · 2015 · PMID 26237428 · open access
페이지 2개
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level
Schröder J,
Chegwidden L,
Maj C,
Gehlen J,
Speller J,
Böhmer AC,
Borisov O,
Hess T,
Kreuser N,
Venerito M,
Alakus H,
May A
외 56명 — 모두 보기
Gerges C,
Schmidt T,
Thieme R,
Heider D,
Hillmer AM,
Reingruber J,
Lyros O,
Dietrich A,
Hoffmeister A,
Mehdorn M,
Lordick F,
Stocker G,
Hohaus M,
Reim D,
Kandler J,
Müller M,
Ebigbo A,
Fuchs C,
Bruns CJ,
Hölscher AH,
Lang H,
Grimminger PP,
Dakkak D,
Vashist Y,
May S,
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GWAS of Dizygotic Twinning in an Enlarged Australian Sample of Mothers of DZ Twins
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Exploring the Germline Genetics of In Situ and Invasive Cutaneous Melanoma: A Genome-Wide Association Study Meta-Analysis
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외 2명 — 모두 보기
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