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2,673 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.
53 matches for
Ma R,
showing the first 13.
A type 1 diabetes genetic risk score discriminates between type 1 diabetes and type 2 diabetes in a Chinese population
Hu J,
Jiang G,
Qin J,
Luo S,
Fan B,
Xie Z,
Wan R,
Li X,
Tam CHT,
Wang Z,
Ding J,
Xia Y
and 16 more — show all
Yang Y,
Lin J,
Yu G,
Jin P,
Lim CKP,
Luk AOY,
So WY,
Chan JCN,
Wang C,
Huang J,
Weedon MN,
Hagopian WA,
Oram RA,
Ma RCW,
Xiao Y,
Zhou Z
Hong Kong Diabetes Biobank Study Group
Diabetologia · 2025 · PMID 40569436 · open access
2 pages
Common variation at 10p12.31 near MLLT10 influences meningioma risk
Dobbins SE,
Broderick P,
Melin B,
Feychting M,
Johansen C,
Andersson U,
Brännström T,
Schramm J,
Olver B,
Lloyd A,
Ma YP,
Hosking FJ
and 15 more — show all
Lönn S,
Ahlbom A,
Henriksson R,
Schoemaker MJ,
Hepworth SJ,
Hoffmann P,
Mühleisen TW,
Nöthen MM,
Moebus S,
Eisele L,
Kosteljanetz M,
Muir K,
Swerdlow A,
Simon M,
Houlston RS
Nature genetics · 2011 · PMID 21804547 · open access
1 page
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Cho YS,
Chen CH,
Hu C,
Long J,
Ong RT,
Sim X,
Takeuchi F,
Wu Y,
Go MJ,
Yamauchi T,
Chang YC,
Kwak SH
and 56 more — show all
Ma RC,
Yamamoto K,
Adair LS,
Aung T,
Cai Q,
Chang LC,
Chen YT,
Gao Y,
Hu FB,
Kim HL,
Kim S,
Kim YJ,
Lee JJ,
Lee NR,
Li Y,
Liu JJ,
Lu W,
Nakamura J,
Nakashima E,
Ng DP,
Tay WT,
Tsai FJ,
Wong TY,
Yokota M,
Zheng W,
Zheng W,
Zhang R,
Wang C,
So WY,
Ohnaka K,
Ikegami H,
Hara K,
Cho YM,
Cho NH,
Chang TJ,
Bao Y,
Hedman ÅK,
Morris AP,
McCarthy MI,
Takayanagi R,
Park KS,
Jia W,
Chuang LM,
Chuang LM,
Chan JC,
Maeda S,
Kadowaki T,
Lee JY,
Wu JY,
Teo YY,
Tai ES,
Shu XO,
Mohlke KL,
Kato N,
Han BG,
Seielstad M
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4
Ellinghaus D,
Folseraas T,
Holm K,
Ellinghaus E,
Melum E,
Balschun T,
Laerdahl JK,
Shiryaev A,
Gotthardt DN,
Weismüller TJ,
Schramm C,
Wittig M
and 25 more — show all
Bergquist A,
Björnsson E,
Marschall HU,
Vatn M,
Teufel A,
Rust C,
Gieger C,
Wichmann HE,
Runz H,
Sterneck M,
Rupp C,
Braun F,
Weersma RK,
Wijmenga C,
Ponsioen CY,
Mathew CG,
Rutgeerts P,
Vermeire S,
Schrumpf E,
Hov JR,
Manns MP,
Boberg KM,
Schreiber S,
Franke A,
Karlsen TH
Hepatology (Baltimore, Md.) · 2013 · PMID 22821403
1 page
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
Heap GA,
Weedon MN,
Bewshea CM,
Singh A,
Chen M,
Satchwell JB,
Vivian JP,
So K,
Dubois PC,
Andrews JM,
Annese V,
Bampton P
and 44 more — show all
Barnardo M,
Bell S,
Cole A,
Connor SJ,
Creed T,
Cummings FR,
D'Amato M,
Daneshmend TK,
Fedorak RN,
Florin TH,
Gaya DR,
Greig E,
Halfvarson J,
Hart A,
Irving PM,
Jones G,
Karban A,
Lawrance IC,
Lee JC,
Lees C,
Lev-Tzion R,
Lindsay JO,
Mansfield J,
Mawdsley J,
Mazhar Z,
Parkes M,
Parnell K,
Orchard TR,
Radford-Smith G,
Russell RK,
Reffitt D,
Satsangi J,
Silverberg MS,
Sturniolo GC,
Tremelling M,
Tsianos EV,
van Heel DA,
Walsh A,
Watermeyer G,
Weersma RK,
Zeissig S,
Rossjohn J,
Holden AL,
Ahmad T
International Serious Adverse Events Consortium · IBD Pharmacogenetics Study Group
Nature genetics · 2014 · PMID 25217962
1 page
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos
Gao X,
Nannini DR,
Corrao K,
Torres M,
Chen YI,
Fan BJ,
Wiggs JL,
Taylor KD,
Gauderman WJ,
Rotter JI,
Varma R
International Glaucoma Genetics Consortium
Human molecular genetics · 2016 · PMID 28171582
1 page
Splicing variant of <i>WDFY4</i> augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis
Kochi Y,
Kamatani Y,
Kondo Y,
Suzuki A,
Kawakami E,
Hiwa R,
Momozawa Y,
Fujimoto M,
Jinnin M,
Tanaka Y,
Kanda T,
Cooper RG
and 36 more — show all
Chinoy H,
Rothwell S,
Lamb JA,
Vencovský J,
Mann H,
Ohmura K,
Myouzen K,
Ishigaki K,
Nakashima R,
Hosono Y,
Tsuboi H,
Kawasumi H,
Iwasaki Y,
Kajiyama H,
Horita T,
Ogawa-Momohara M,
Takamura A,
Tsunoda S,
Shimizu J,
Fujio K,
Amano H,
Mimori A,
Kawakami A,
Umehara H,
Takeuchi T,
Sano H,
Muro Y,
Atsumi T,
Mimura T,
Kawaguchi Y,
Mimori T,
Takahashi A,
Kubo M,
Kohsaka H,
Sumida T,
Yamamoto K
Annals of the rheumatic diseases · 2018 · PMID 29331962
1 page
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
Ahlqvist E,
Sandholm N,
Deshmukh H,
Rayner NW,
Abdalla M,
Ladenvall C,
Ziemek D,
Fauman E,
Robertson NR,
McKeigue PM,
Valo E
and 69 more — show all
Forsblom C,
Harjutsalo V,
Perna A,
Rurali E,
Marcovecchio ML,
Igo RP Jr,
Salem RM,
Perico N,
Lajer M,
Käräjämäki A,
Imamura M,
Kubo M,
Takahashi A,
Sim X,
Liu J,
van Dam RM,
Jiang G,
Tam CHT,
Luk AOY,
Lee HM,
Lim CKP,
Szeto CC,
So WY,
Chan JCN,
Ang SF,
Dorajoo R,
Wang L,
Clara TSH,
McKnight AJ,
Duffy S,
Pezzolesi MG,
Marre M,
Gyorgy B,
Hadjadj S,
Hiraki LT,
Ahluwalia TS,
Almgren P,
Schulz CA,
Orho-Melander M,
Linneberg A,
Christensen C,
Witte DR,
Grarup N,
Brandslund I,
Melander O,
Paterson AD,
Tregouet D,
Maxwell AP,
Lim SC,
Ma RCW,
Tai ES,
Maeda S,
Lyssenko V,
Tuomi T,
Krolewski AS,
Rich SS,
Hirschhorn JN,
Florez JC,
Dunger D,
Pedersen O,
Hansen T,
Rossing P,
Remuzzi G,
Brosnan MJ,
Palmer CNA,
Groop PH,
Colhoun HM,
Groop LC,
McCarthy MI
Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group and 4 more consortia
Diabetes · 2018 · PMID 29703844
1 page
Alcohol Intake Interacts with Functional Genetic Polymorphisms of Aldehyde Dehydrogenase (ALDH2) and Alcohol Dehydrogenase (ADH) to Increase Esophageal Squamous Cell Cancer Risk
Suo C,
Yang Y,
Yuan Z,
Zhang T,
Yang X,
Qing T,
Gao P,
Shi L,
Fan M,
Cheng H,
Lu M,
Jin L
and 2 more — show all
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2019 · PMID 30639619
1 page
Germline variants at SOHLH2 influence multiple myeloma risk
Duran-Lozano L,
Thorleifsson G,
Lopez de Lapuente Portilla A,
Niroula A,
Went M,
Thodberg M,
Pertesi M,
Ajore R,
Cafaro C,
Olason PI,
Stefansdottir L,
Bragi Walters G
and 15 more — show all
Halldorsson GH,
Turesson I,
Kaiser MF,
Weinhold N,
Abildgaard N,
Andersen NF,
Mellqvist UH,
Waage A,
Juul-Vangsted A,
Thorsteinsdottir U,
Hansson M,
Houlston R,
Rafnar T,
Stefansson K,
Nilsson B
Blood cancer journal · 2021 · PMID 33875642 · open access
1 page
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
Liao C,
Castonguay CE,
Heilbron K,
Vuokila V,
Medeiros M,
Houle G,
Akçimen F,
Ross JP,
Catoire H,
Diez-Fairen M,
Kang J,
Mueller SH
and 36 more — show all
Girard SL,
Hopfner F,
Lorenz D,
Clark LN,
Soto-Beasley AI,
Klebe S,
Hallett M,
Wszolek ZK,
Pendziwiat M,
Lorenzo-Betancor O,
Seppi K,
Berg D,
Vilariño-Güell C,
Postuma RB,
Bernard G,
Dupré N,
Jankovic J,
Testa CM,
Ross OA,
Arzberger T,
Chouinard S,
Louis ED,
Mandich P,
Vitale C,
Barone P,
García-Martín E,
Alonso-Navarro H,
Agúndez JAG,
Jiménez-Jiménez FJ,
Pastor P,
Rajput A,
Deuschl G,
Kuhlenbaümer G,
Meijer IA,
Dion PA,
Rouleau GA
23andMe Research Team
JAMA neurology · 2022 · PMID 34982113 · open access
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.