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578 matches for
An J,
showing the first 18.
Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-related Traits Identifies Novel Risk Loci in Han Chinese Individuals
Xu H,
Liu F,
Li Z,
Li X,
Liu Y,
Li N,
Zhang X,
Gao Z,
Zhang X,
Liu Y,
Zou J,
Meng L
and 13 more — show all
Liu S,
Zhu H,
Tang X,
Wu H,
Su K,
Chen B,
Yu D,
Ye H,
Chen H,
Yi H,
Yin S,
Guan J,
Shi Y
American journal of respiratory and critical care medicine · 2022 · PMID 35819321
1 page
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
and 128 more — show all
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
1 page
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
Pan H,
Liu Z,
Ma J,
Li Y,
Zhao Y,
Zhou X,
Xiang Y,
Wang Y,
Zhou X,
He R,
Xie Y,
Zhou Q
and 48 more — show all
Yuan K,
Xu Q,
Sun Q,
Wang J,
Yan X,
Zhang H,
Wang C,
Lei L,
Liu W,
Wang X,
Ding X,
Wang T,
Xue Z,
Zhang Z,
Chen L,
Wang Q,
Liu Y,
Tang J,
Zhang X,
Peng S,
Wang C,
Ding J,
Liu C,
Wang L,
Chen H,
Shen L,
Jiang H,
Wu X,
Tan H,
Luo D,
Xiao S,
Chen X,
Tan J,
Hu Z,
Chen C,
Xia K,
Zhang Z,
Foo JN,
Blauwendraat C,
Nalls MA,
Singleton AB,
Liu J,
Chan P,
Zheng H,
Li J,
Guo J,
Yang J,
Tang B
Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)
NPJ Parkinson's disease · 2023 · PMID 36759515 · open access
1 page
Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions
Lindström S,
Wang L,
Feng H,
Majumdar A,
Huo S,
Macdonald J,
Harrison T,
Turman C,
Chen H,
Mancuso N,
Bammler T,
Gallinger S
and 49 more — show all
Gruber SB,
Gunter MJ,
Le Marchand L,
Moreno V,
Offit K,
De Vivo I,
O'Mara TA,
Spurdle AB,
Tomlinson I,
Fitzgerald R,
Gharahkhani P,
Gockel I,
Jankowski J,
Macgregor S,
Schumacher J,
Barnholtz-Sloan J,
Bondy ML,
Houlston RS,
Jenkins RB,
Melin B,
Wrensch M,
Brennan P,
Christiani DC,
Johansson M,
Mckay J,
Aldrich MC,
Amos CI,
Landi MT,
Tardon A,
Bishop DT,
Demenais F,
Goldstein AM,
Iles MM,
Kanetsky PA,
Law MH,
Amundadottir LT,
Stolzenberg-Solomon R,
Wolpin BM,
Klein A,
Petersen G,
Risch H,
Chanock SJ,
Purdue MP,
Scelo G,
Pharoah P,
Kar S,
Hung RJ,
Pasaniuc B,
Kraft P
Breast Cancer Association Consortium (BCAC) · Colorectal Transdisciplinary Study (CORECT), Colon Cancer Family Registry Study (CCFR), Genetics And Epidemiology Of Colorectal Cancer Consortium (GECCO) and 5 more consortia
Journal of the National Cancer Institute · 2023 · PMID 36929942
1 page
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
Joo YY,
Pacheco JA,
Thompson WK,
Rasmussen-Torvik LJ,
Rasmussen LV,
Lin FTJ,
Andrade M,
Borthwick KM,
Bottinger E,
Cagan A,
Carrell DS,
Denny JC
and 13 more — show all
Ellis SB,
Gottesman O,
Linneman JG,
Pathak J,
Peissig PL,
Shang N,
Tromp G,
Veerappan A,
Smith ME,
Chisholm RL,
Gawron AJ,
Hayes MG,
Kho AN
PloS one · 2023 · PMID 37196047 · open access
1 page
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
Braund PS,
Sadeg-Sayoud I,
Iismaa SE,
Kosel ML,
Zhou X,
Hamby SE,
Cheng J,
Liu L,
Tarr I,
Muller DWM,
d'Escamard V,
King A,
Brunham LR,
Baranowska-Clarke AA,
Debette S,
Amouyel P,
Olin JW,
Patil S,
Hesselson SE,
Junday K,
Kanoni S,
Aragam KG,
Butterworth AS,
Tweet MS,
Gulati R,
Combaret N,
Kadian-Dodov D,
Kalman JM,
Fatkin D,
Hingorani AD,
Saw J,
Webb TR,
Hayes SN,
Yang X,
Ganesh SK,
Olson TM,
Kovacic JC,
Graham RM,
Samani NJ,
Bouatia-Naji N
CARDIoGRAMPlusC4D · MEGASTROKE and 2 more consortia
Nature genetics · 2023 · PMID 37248441 · open access
1 page
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake
Williamson A,
Norris DM,
Yin X,
Broadaway KA,
Moxley AH,
Vadlamudi S,
Wilson EP,
Jackson AU,
Ahuja V,
Andersen MK,
Arzumanyan Z,
Bonnycastle LL
and 103 more — show all
Bornstein SR,
Bretschneider MP,
Buchanan TA,
Chang YC,
Chuang LM,
Chung RH,
Clausen TD,
Damm P,
Delgado GE,
de Mello VD,
Dupuis J,
Dwivedi OP,
Erdos MR,
Fernandes Silva L,
Frayling TM,
Gieger C,
Goodarzi MO,
Guo X,
Gustafsson S,
Hakaste L,
Hammar U,
Hatem G,
Herrmann S,
Højlund K,
Horn K,
Hsueh WA,
Hung YJ,
Hwu CM,
Jonsson A,
Kårhus LL,
Kleber ME,
Kovacs P,
Lakka TA,
Lauzon M,
Lee IT,
Lindgren CM,
Lindström J,
Linneberg A,
Liu CT,
Luan J,
Aly DM,
Mathiesen E,
Moissl AP,
Morris AP,
Narisu N,
Perakakis N,
Peters A,
Prasad RB,
Rodionov RN,
Roll K,
Rundsten CF,
Sarnowski C,
Savonen K,
Scholz M,
Sharma S,
Stinson SE,
Suleman S,
Tan J,
Taylor KD,
Uusitupa M,
Vistisen D,
Witte DR,
Walther R,
Wu P,
Xiang AH,
Zethelius B,
Ahlqvist E,
Bergman RN,
Chen YI,
Collins FS,
Fall T,
Florez JC,
Fritsche A,
Grallert H,
Groop L,
Hansen T,
Koistinen HA,
Komulainen P,
Laakso M,
Lind L,
Loeffler M,
März W,
Meigs JB,
Raffel LJ,
Rauramaa R,
Rotter JI,
Schwarz PEH,
Stumvoll M,
Sundström J,
Tönjes A,
Tuomi T,
Tuomilehto J,
Wagner R,
Barroso I,
Walker M,
Grarup N,
Boehnke M,
Wareham NJ,
Mohlke KL,
Wheeler E,
O'Rahilly S,
Fazakerley DJ,
Langenberg C
Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37291194 · open access
1 page
Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations
Chen WC,
Brandenburg JT,
Choudhury A,
Hayat M,
Sengupta D,
Swiel Y,
Babb de Villiers C,
Ferndale L,
Aldous C,
Soo CC,
Lee S,
Curtis C
and 10 more — show all
American journal of human genetics · 2023 · PMID 37673066
1 page
Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry
Brandenburg JT,
Chen WC,
Boua PR,
Govender MA,
Agongo G,
Micklesfield LK,
Sorgho H,
Tollman S,
Asiki G,
Mashinya F,
Hazelhurst S,
Morris AP
and 2 more — show all
Frontiers in genetics · 2024 · PMID 38812969 · open access
1 page
Meta-analysis of genome-wide association studies of stable warfarin dose in patients of African ancestry
Asiimwe IG,
Blockman M,
Cavallari LH,
Cohen K,
Cupido C,
Dandara C,
Davis BH,
Jacobson B,
Johnson JA,
Lamorde M,
Limdi NA,
Morgan J
and 15 more — show all
Mouton JP,
Muyambo S,
Nakagaayi D,
Ndadza A,
Okello E,
Perera MA,
Schapkaitz E,
Sekaggya-Wiltshire C,
Semakula JR,
Tatz G,
Waitt C,
Yang G,
Zhang EJ,
Jorgensen AL,
Pirmohamed M
Blood advances · 2024 · PMID 39163621 · open access
1 page
Treatment of restless legs syndrome and periodic limb movement disorder: an American Academy of Sleep Medicine clinical practice guideline
Winkelman JW,
Berkowski JA,
DelRosso LM,
Koo BB,
Scharf MT,
Sharon D,
Zak RS,
Kazmi U,
Falck-Ytter Y,
Shelgikar AV,
Trotti LM,
Walters AS
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2025 · PMID 39324694
1 page
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
and 113 more — show all
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
1 page
Genome-wide association study reveals genetic architecture and evolution of human retinal pigmentation
Yuan J,
Zhang Y,
Yao Y,
Li S,
Liang J,
Dai W,
Yang J,
Liu M,
Zhang Q,
Zhou Y,
Li J,
Liu H
and 5 more — show all
Myopia Associated Genetics and Intervention Consortium
Science advances · 2026 · PMID 41477839 · open access
1 page
Oculocutaneous albinism variants in 28 consanguineous families and functional classification of a pathogenic deep intron variant in TYR
Farooq M,
Bruun GH,
Sarusie MVK,
Kessel L,
Akhtar H,
Abdullah U,
Ali Z,
Shah SA,
Ali N,
Anjum I,
Doktor TK,
Andresen BS
and 3 more — show all
European journal of human genetics : EJHG · 2026 · PMID 41807736 · 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.