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2,662 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
8 matches for
Neale RE.
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
12 pages+
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
and 140 more — show all
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 and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis
Ong JS,
An J,
Han X,
Law MH,
Nandakumar P,
Schumacher J,
Gockel I,
Bohmer A,
Jankowski J,
Palles C,
Olsen CM,
Neale RE
and 8 more — show all
23andMe Research team · Esophageal cancer consortium
Gut · 2022 · PMID 34187846 · open access
8 pages
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Klein AP,
Wolpin BM,
Risch HA,
Stolzenberg-Solomon RZ,
Mocci E,
Zhang M,
Canzian F,
Childs EJ,
Hoskins JW,
Jermusyk A,
Zhong J,
Chen F
and 112 more — show all
Albanes D,
Andreotti G,
Arslan AA,
Babic A,
Bamlet WR,
Beane-Freeman L,
Berndt SI,
Blackford A,
Borges M,
Borgida A,
Bracci PM,
Brais L,
Brennan P,
Brenner H,
Bueno-de-Mesquita B,
Buring J,
Campa D,
Capurso G,
Cavestro GM,
Chaffee KG,
Chung CC,
Cleary S,
Cotterchio M,
Dijk F,
Duell EJ,
Foretova L,
Fuchs C,
Funel N,
Gallinger S,
M Gaziano JM,
Gazouli M,
Giles GG,
Giovannucci E,
Goggins M,
Goodman GE,
Goodman PJ,
Hackert T,
Haiman C,
Hartge P,
Hasan M,
Hegyi P,
Helzlsouer KJ,
Herman J,
Holcatova I,
Holly EA,
Hoover R,
Hung RJ,
Jacobs EJ,
Jamroziak K,
Janout V,
Kaaks R,
Khaw KT,
Klein EA,
Kogevinas M,
Kooperberg C,
Kulke MH,
Kupcinskas J,
Kurtz RJ,
Laheru D,
Landi S,
Lawlor RT,
Lee IM,
LeMarchand L,
Lu L,
Malats N,
Mambrini A,
Mannisto S,
Milne RL,
Mohelníková-Duchoňová B,
Neale RE,
Neoptolemos JP,
Oberg AL,
Olson SH,
Orlow I,
Pasquali C,
Patel AV,
Peters U,
Pezzilli R,
Porta M,
Real FX,
Rothman N,
Scelo G,
Sesso HD,
Severi G,
Shu XO,
Silverman D,
Smith JP,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Tavano F,
Thornquist MD,
Tobias GS,
Van Den Eeden SK,
Vashist Y,
Visvanathan K,
Vodicka P,
Wactawski-Wende J,
Wang Z,
Wentzensen N,
White E,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Zheng W,
Zheng W,
Kraft P,
Li D,
Chanock S,
Obazee O,
Petersen GM,
Amundadottir LT
Nature communications · 2018 · PMID 29422604 · open access
4 pages
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
and 6 more — show all
BEACON · 23andMe Research Team
Nature communications · 2019 · PMID 31527586 · open access
4 pages
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Childs EJ,
Mocci E,
Campa D,
Bracci PM,
Gallinger S,
Goggins M,
Li D,
Neale RE,
Olson SH,
Scelo G,
Amundadottir LT,
Bamlet WR
and 50 more — show all
Bijlsma MF,
Blackford A,
Borges M,
Brennan P,
Brenner H,
Bueno-de-Mesquita HB,
Canzian F,
Capurso G,
Cavestro GM,
Chaffee KG,
Chanock SJ,
Cleary SP,
Cotterchio M,
Foretova L,
Fuchs C,
Funel N,
Gazouli M,
Hassan M,
Herman JM,
Holcatova I,
Holly EA,
Hoover RN,
Hung RJ,
Janout V,
Key TJ,
Kupcinskas J,
Kurtz RC,
Landi S,
Lu L,
Malecka-Panas E,
Mambrini A,
Mohelnikova-Duchonova B,
Neoptolemos JP,
Oberg AL,
Orlow I,
Pasquali C,
Pezzilli R,
Rizzato C,
Saldia A,
Scarpa A,
Stolzenberg-Solomon RZ,
Strobel O,
Tavano F,
Vashist YK,
Vodicka P,
Wolpin BM,
Yu H,
Petersen GM,
Risch HA,
Klein AP
Nature genetics · 2015 · PMID 26098869 · open access
3 pages
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Zhang M,
Wang Z,
Obazee O,
Jia J,
Childs EJ,
Hoskins J,
Figlioli G,
Mocci E,
Collins I,
Chung CC,
Hautman C,
Arslan AA
and 112 more — show all
Beane-Freeman L,
Bracci PM,
Buring J,
Duell EJ,
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Kamineni A,
Kolonel LN,
Kulke MH,
Malats N,
Olson SH,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Brais L,
Bueno-de-Mesquita HB,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Bijlsma MF,
Brenner H,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Cavestro GM,
Cotterchio M,
Costello E,
Elena J,
Boggi U,
Gaziano JM,
Gazouli M,
Giovannucci EL,
Goggins M,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Hu N,
Hunter DJ,
Iskierka-Jazdzewska E,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Neale RE,
Oberg AL,
Panico S,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Porta M,
Purdue M,
Quiros JR,
Riboli E,
Rothman N,
Scarpa A,
Scelo G,
Shu XO,
Silverman DT,
Soucek P,
Strobel O,
Sund M,
Małecka-Panas E,
Taylor PR,
Tavano F,
Travis RC,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vashist Y,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Kooperberg C,
Risch HA,
Jacobs EJ,
Li D,
Fuchs C,
Hoover R,
Hartge P,
Chanock SJ,
Petersen GM,
Stolzenberg-Solomon RS,
Wolpin BM,
Kraft P,
Klein AP,
Canzian F,
Amundadottir LT
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
Exploring the Germline Genetics of In Situ and Invasive Cutaneous Melanoma: A Genome-Wide Association Study Meta-Analysis
Ingold N,
Seviiri M,
Ong JS,
Neale RE,
Pandeya N,
Whiteman DC,
Olsen CM,
Martin NG,
Duffy DL,
Khosrotehrani K,
Hayward N,
Montgomery GW
and 2 more — show all
JAMA dermatology · 2024 · PMID 39141363
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.