For researchers

Is your paper here?

2,665 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.

270 matches for Ng M, showing the first 20.

Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy

Schoeler NE, Leu C, Balestrini S, Mudge JM, Steward CA, Frankish A, Leung MA, Mackay M, Scheffer I, Williams R, Sander JW, Cross JH

and 1 more — show all

Sisodiya SM

Epilepsia · 2018 · PMID 30009487

1 page

rs12204701

A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin

Oskarsson GR, Kristjansson RP, Lee AL, Sveinbjornsson G, Magnusson MK, Ivarsdottir EV, Benonisdottir S, Oddsson A, Davidsson OB, Saemundsdottir J, Halldorsson GH, Arthur J

and 11 more — show all

Arnadottir GA, Masson G, Jensson BO, Holm H, Olafsson I, Onundarson PT, Gudbjartsson DF, Norddahl GL, Thorsteinsdottir U, Sulem P, Stefansson K

Communications biology · 2018 · PMID 30271932 · open access

1 page

rs370865377

Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis

Wang C, Zheng X, Jiang P, Tang R, Gong Y, Dai Y, Wang L, Xu P, Sun W, Wang L, Han C, Jiang Y

and 39 more — show all

Wei Y, Zhang K, Wu J, Shao Y, Gao Y, Yu J, Hu Z, Zang Z, Zhao Y, Wu X, Dai N, Liu L, Nie J, Jiang B, Lin M, Li L, Li Y, Chen S, Shu L, Qiu F, Wu Q, Zhang M, Chen R, Jawed R, Zhang Y, Shi X, Zhu Z, Pei H, Huang L, Zhao W, Tian Y, Zhu X, Qiu H, Gershwin ME, Chen W, Seldin MF, Liu X, Sun L, Ma X

Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access

1 page

rs1794280

Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study

Zhu M, Xu K, Chen Y, Gu Y, Zhang M, Luo F, Liu Y, Gu W, Hu J, Xu H, Xie Z, Sun C

and 42 more — show all

Li Y, Sun M, Xu X, Hsu HT, Chen H, Fu Q, Shi Y, Xu J, Ji L, Liu J, Bian L, Zhu J, Chen S, Xiao L, Li X, Jiang H, Shen M, Huang Q, Fang C, Li X, Huang G, Fan J, Jiang Z, Jiang Y, Dai J, Ma H, Zheng S, Cai Y, Dai H, Zheng X, Zhou H, Ni S, Jin G, She JX, Yu L, Polychronakos C, Hu Z, Zhou Z, Weng J, Weng J, Shen H, Yang T

Diabetes care · 2019 · PMID 31152121

1 page

rs4320356

Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations

Yan C, Zhu M, Ding Y, Yang M, Wang M, Li G, Ren C, Huang T, Yang W, He B, Wang M, Yu F

and 22 more — show all

Wang J, Zhang R, Wang T, Ni J, Chen J, Jiang Y, Dai J, Zhang E, Ma H, Wang Y, Xu D, Wang S, Chen Y, Xu Z, Zhou J, Ji G, Wang Z, Zhang Z, Hu Z, Wei Q, Shen H, Jin G

Gut · 2020 · PMID 31383772

1 page

rs10029005

Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry

Hauser MA, Allingham RR, Aung T, Van Der Heide CJ, Taylor KD, Rotter JI, Wang SJ, Bonnemaijer PWM, Williams SE, Abdullahi SM, Abu-Amero KK, Anderson MG

and 81 more — show all

Akafo S, Alhassan MB, Asimadu I, Ayyagari R, Bakayoko S, Nyamsi PB, Bowden DW, Bromley WC, Budenz DL, Carmichael TR, Challa P, Chen YI, Chuka-Okosa CM, Cooke Bailey JN, Costa VP, Cruz DA, DuBiner H, Ervin JF, Feldman RM, Flamme-Wiese M, Gaasterland DE, Garnai SJ, Girkin CA, Guirou N, Guo X, Haines JL, Hammond CJ, Herndon L, Hoffmann TJ, Hulette CM, Hydara A, Igo RP Jr, Jorgenson E, Kabwe J, Kilangalanga NJ, Kizor-Akaraiwe N, Kuchtey RW, Lamari H, Li Z, Liebmann JM, Liu Y, Loos RJF, Melo MB, Moroi SE, Msosa JM, Mullins RF, Nadkarni G, Napo A, Ng MCY, Nunes HF, Obeng-Nyarkoh E, Okeke A, Okeke S, Olaniyi O, Olawoye O, Oliveira MB, Pasquale LR, Perez-Grossmann RA, Pericak-Vance MA, Qin X, Ramsay M, Resnikoff S, Richards JE, Schimiti RB, Sim KS, Sponsel WE, Svidnicki PV, Thiadens AAHJ, Uche NJ, van Duijn CM, de Vasconcellos JPC, Wiggs JL, Zangwill LM, Risch N, Milea D, Ashaye A, Klaver CCW, Weinreb RN, Ashley Koch AE, Fingert JH, Khor CC

Genetics of Glaucoma in People of African Descent (GGLAD) Consortium

JAMA · 2019 · PMID 31688885

1 page

rs59892895

The influence of rare variants in circulating metabolic biomarkers

Riveros-Mckay F, Oliver-Williams C, Karthikeyan S, Walter K, Kundu K, Ouwehand WH, Roberts D, Di Angelantonio E, Soranzo N, Danesh J, Wheeler E, Zeggini E

and 2 more — show all

Butterworth AS, Barroso I

INTERVAL Study

PLoS genetics · 2020 · PMID 32150548 · open access

1 page

rs12191266

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

Keene KL, Hyacinth HI, Bis JC, Kittner SJ, Mitchell BD, Cheng YC, Pare G, Chong M, O'Donnell M, Meschia JF, Chen WM, Sale MM

and 35 more — show all

COMPASS, SiGN, and METASTROKE Consortia

Stroke · 2020 · PMID 32693751

1 page

rs55931441

Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma

Lin SH, Sampson JN, Grünewald TGP, Surdez D, Reynaud S, Mirabeau O, Karlins E, Rubio RA, Zaidi S, Grossetête-Lalami S, Ballet S, Lapouble E

and 44 more — show all

PloS one · 2020 · PMID 32881892 · open access

1 page

rs78119607

Genome-Wide Association Study of Susceptibility Loci for TCF3-PBX1 Acute Lymphoblastic Leukemia in Children

Lee SHR, Qian M, Yang W, Diedrich JD, Raetz E, Yang W, Dong Q, Devidas M, Pei D, Yeoh A, Cheng C, Pui CH

and 7 more — show all

Evans WE, Mullighan CG, Hunger SP, Savic D, Relling MV, Loh ML, Yang JJ

Journal of the National Cancer Institute · 2021 · PMID 32882024

1 page

rs2665658

Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

Saw J, Yang ML, Trinder M, Tcheandjieu C, Xu C, Starovoytov A, Birt I, Mathis MR, Hunker KL, Schmidt EM, Jackson L, Fendrikova-Mahlay N

and 15 more — show all

Zawistowski M, Brummett CM, Zoellner S, Katz A, Coleman DM, Swan K, Swan K, O'Donnell CJ, Zhou X, Li JZ, Gornik HL, Assimes TL, Stanley JC, Brunham LR, Ganesh SK

Million Veteran Program

Nature communications · 2020 · PMID 32887874 · open access

1 page

rs12740679

Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study

Jin G, Lv J, Yang M, Wang M, Zhu M, Wang T, Yan C, Yu C, Ding Y, Li G, Ren C, Ni J

and 22 more — show all

Zhang R, Guo Y, Bian Z, Zheng Y, Zhang N, Jiang Y, Chen J, Wang Y, Xu D, Zheng H, Yang L, Chen Y, Walters R, Millwood IY, Dai J, Ma H, Chen K, Chen Z, Hu Z, Wei Q, Shen H, Li L

The Lancet. Oncology · 2020 · PMID 33002439

1 page

rs10074991

Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene

Boer CG, Yau MS, Rice SJ, Coutinho de Almeida R, Cheung K, Styrkarsdottir U, Southam L, Broer L, Wilkinson JM, Uitterlinden AG, Zeggini E, Felson D

and 5 more — show all

Loughlin J, Young M, Capellini TD, Meulenbelt I, van Meurs JB

Annals of the rheumatic diseases · 2021 · PMID 33055079 · open access

1 page

rs10916199

Class II Human Leukocyte Antigen Variants Associate With Risk of Pegaspargase Hypersensitivity

Liu Y, Yang W, Smith CA, Cheng C, Karol SE, Larsen EC, Winick N, Carroll WL, Loh ML, Raetz EA, Hunger SP, Winter SS

and 8 more — show all

Dunsmore KP, Devidas M, Yang JJ, Evans WE, Jeha S, Pui CH, Inaba H, Relling MV

Clinical pharmacology and therapeutics · 2021 · PMID 33768542

1 page

rs28383308

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Cade BE, Lee J, Sofer T, Wang H, Zhang M, Chen H, Gharib SA, Gottlieb DJ, Guo X, Lane JM, Liang J, Lin X

and 27 more — show all

NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Sleep Working Group

Genome medicine · 2021 · PMID 34446064 · open access

1 page

rs116133558

Unique motif shared by HLA-B*59:01 and HLA-B*55:02 is associated with methazolamide-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese

Jiang M, Yang F, Zhang L, Xu D, Jia Y, Cheng Y, Han S, Wang T, Chen Z, Su Y, Zhu Z, Chen S

and 6 more — show all

Zhang J, Wang L, Yang L, Yang J, Luo X, Xing Q

Journal of the European Academy of Dermatology and Venereology : JEADV · 2022 · PMID 35122707

1 page

rs2074494

Shared genetic architectures of subjective well-being in East Asian and European ancestry populations

Kim S, Kim K, Hwang MY, Ko H, Jung SH, Shim I, Cha S, Lee H, Kim B, Yoon J, Ha TH, Kim DK

and 7 more — show all

Kim J, Park WY, Okbay A, Kim BJ, Kim YJ, Myung W, Won HH

Nature human behaviour · 2022 · PMID 35589828

1 page

rs7189864

Coenzyme Q10 Supplementation in Statin Treated Patients: A Double-Blinded Randomized Placebo-Controlled Trial

Dohlmann TL, Kuhlman AB, Morville T, Dahl M, Asping M, Orlando P, Silvestri S, Tiano L, Helge JW, Dela F, Larsen S

Antioxidants (Basel, Switzerland) · 2022 · PMID 36139772 · open access

1 page

Coenzyme Q10

Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population

Bai H, Song M, Lei S, Jiao L, Hu X, Wu T, Song J, Liu T, Peng W, Zhao Z, Meng Z, Ying B

MedComm · 2023 · PMID 37009413 · open access

1 page

rs75609205

Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation

Adlam D, Berrandou TE, Georges A, Nelson CP, Giannoulatou E, Henry J, Ma L, Blencowe M, Turley TN, Yang ML, Chopade S, Finan C

and 40 more — show all

CARDIoGRAMPlusC4D · MEGASTROKE and 2 more consortia

Nature genetics · 2023 · PMID 37248441 · open access

1 page

rs7326444

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.