For researchers
Is your paper here?
2,660 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.
11 matches for
Wolford BN.
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Nielsen JB,
Thorolfsdottir RB,
Fritsche LG,
Zhou W,
Skov MW,
Graham SE,
Herron TJ,
McCarthy S,
Schmidt EM,
Sveinbjornsson G,
Surakka I,
Mathis MR
and 37 more — show all
Yamazaki M,
Crawford RD,
Gabrielsen ME,
Skogholt AH,
Holmen OL,
Lin M,
Wolford BN,
Dey R,
Dalen H,
Sulem P,
Chung JH,
Backman JD,
Arnar DO,
Thorsteinsdottir U,
Baras A,
O'Dushlaine C,
Holst AG,
Wen X,
Hornsby W,
Dewey FE,
Boehnke M,
Kheterpal S,
Mukherjee B,
Lee S,
Kang HM,
Holm H,
Kitzman J,
Shavit JA,
Jalife J,
Brummett CM,
Teslovich TM,
Carey DJ,
Gudbjartsson DF,
Stefansson K,
Abecasis GR,
Hveem K,
Willer CJ
Nature genetics · 2018 · PMID 30061737
12 pages+
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
Zhou W,
Brumpton B,
Kabil O,
Gudmundsson J,
Thorleifsson G,
Weinstock J,
Zawistowski M,
Nielsen JB,
Chaker L,
Medici M,
Teumer A,
Naitza S
and 44 more — show all
Sanna S,
Schultheiss UT,
Cappola A,
Karjalainen J,
Kurki M,
Oneka M,
Taylor P,
Fritsche LG,
Graham SE,
Wolford BN,
Overton W,
Rasheed H,
Haug EB,
Gabrielsen ME,
Skogholt AH,
Surakka I,
Davey Smith G,
Pandit A,
Roychowdhury T,
Hornsby WE,
Jonasson JG,
Senter L,
Liyanarachchi S,
Ringel MD,
Xu L,
Kiemeney LA,
He H,
Netea-Maier RT,
Mayordomo JI,
Plantinga TS,
Hrafnkelsson J,
Hjartarson H,
Sturgis EM,
Palotie A,
Daly M,
Citterio CE,
Arvan P,
Brummett CM,
Boehnke M,
de la Chapelle A,
Stefansson K,
Hveem K,
Willer CJ,
Åsvold BO
Nature communications · 2020 · PMID 32769997 · open access
12 pages+
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors
Thibord F,
Klarin D,
Brody JA,
Chen MH,
Levin MG,
Chasman DI,
Goode EL,
Hveem K,
Teder-Laving M,
Martinez-Perez A,
Aïssi D,
Daian-Bacq D
and 76 more — show all
Ito K,
Natarajan P,
Lutsey PL,
Nadkarni GN,
de Vries PS,
Cuellar-Partida G,
Wolford BN,
Pattee JW,
Kooperberg C,
Braekkan SK,
Li-Gao R,
Saut N,
Sept C,
Germain M,
Judy RL,
Wiggins KL,
Ko D,
O'Donnell CJ,
Taylor KD,
Giulianini F,
De Andrade M,
Nøst TH,
Boland A,
Empana JP,
Koyama S,
Gilliland T,
Do R,
Huffman JE,
Wang X,
Wang X,
Zhou W,
Manuel Soria J,
Carlos Souto J,
Pankratz N,
Haessler J,
Hindberg K,
Rosendaal FR,
Turman C,
Olaso R,
Kember RL,
Bartz TM,
Lynch JA,
Heckbert SR,
Armasu SM,
Brumpton B,
Smadja DM,
Jouven X,
Komuro I,
Clapham KR,
Loos RJF,
Willer CJ,
Sabater-Lleal M,
Pankow JS,
Reiner AP,
Morelli VM,
Ridker PM,
Vlieg AVH,
Deleuze JF,
Kraft P,
Rader DJ,
Min Lee K,
Psaty BM,
Heidi Skogholt A,
Emmerich J,
Suchon P,
Rich SS,
Vy HMT,
Tang W,
Jackson RD,
Hansen JB,
Morange PE,
Kabrhel C,
Trégouët DA,
Damrauer SM,
Johnson AD,
Smith NL
Global Biobank Meta-Analysis Initiative; Estonian Biobank Research Team; 23andMe Research Team; Biobank Japan; CHARGE Hemostasis Working Group
Circulation · 2022 · PMID 36154123
12 pages+
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Aragam KG,
Jiang T,
Goel A,
Kanoni S,
Wolford BN,
Atri DS,
Weeks EM,
Wang M,
Hindy G,
Zhou W,
Grace C,
Roselli C
and 83 more — show all
Marston NA,
Kamanu FK,
Surakka I,
Venegas LM,
Sherliker P,
Koyama S,
Ishigaki K,
Åsvold BO,
Brown MR,
Brumpton B,
de Vries PS,
Giannakopoulou O,
Giardoglou P,
Gudbjartsson DF,
Güldener U,
Haider SMI,
Helgadottir A,
Ibrahim M,
Kastrati A,
Kessler T,
Kyriakou T,
Konopka T,
Li L,
Ma L,
Meitinger T,
Mucha S,
Munz M,
Murgia F,
Nielsen JB,
Nöthen MM,
Pang S,
Reinberger T,
Schnitzler G,
Smedley D,
Thorleifsson G,
von Scheidt M,
Ulirsch JC,
Arnar DO,
Burtt NP,
Costanzo MC,
Flannick J,
Ito K,
Jang DK,
Kamatani Y,
Khera AV,
Komuro I,
Kullo IJ,
Lotta LA,
Nelson CP,
Roberts R,
Thorgeirsson G,
Thorsteinsdottir U,
Webb TR,
Baras A,
Björkegren JLM,
Boerwinkle E,
Dedoussis G,
Holm H,
Hveem K,
Melander O,
Morrison AC,
Orho-Melander M,
Rallidis LS,
Ruusalepp A,
Sabatine MS,
Stefansson K,
Zalloua P,
Ellinor PT,
Farrall M,
Danesh J,
Ruff CT,
Finucane HK,
Hopewell JC,
Clarke R,
Gupta RM,
Erdmann J,
Samani NJ,
Schunkert H,
Watkins H,
Willer CJ,
Deloukas P,
Kathiresan S,
Butterworth AS
Biobank Japan · EPIC-CVD and 1 more consortia
Nature genetics · 2022 · PMID 36474045 · open access
12 pages+
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
and 140 more — show all
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 and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
Atlas of genetic and phenotypic associations across 42 female reproductive health diagnoses
Pujol Gualdo N,
Džigurski J,
Rukins V,
Pajuste FD,
Wolford BN,
Võsa M,
Golob M,
Haug L,
Alver M,
Läll K,
Peters M,
Brumpton BM
and 3 more — show all
Estonian Biobank Research Team
Nature medicine · 2025 · PMID 40069456
12 pages+
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Klarin D,
Verma SS,
Judy R,
Dikilitas O,
Wolford BN,
Paranjpe I,
Levin MG,
Pan C,
Tcheandjieu C,
Spin JM,
Lynch J,
Assimes TL
and 41 more — show all
Åldstedt Nyrønning L,
Mattsson E,
Edwards TL,
Denny J,
Larson E,
Lee MTM,
Carrell D,
Zhang Y,
Jarvik GP,
Gharavi AG,
Harley J,
Mentch F,
Pacheco JA,
Hakonarson H,
Skogholt AH,
Thomas L,
Gabrielsen ME,
Hveem K,
Nielsen JB,
Zhou W,
Fritsche L,
Huang J,
Natarajan P,
Sun YV,
DuVall SL,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Scali ST,
Berceli SA,
Willer C,
Jones GT,
Bown MJ,
Nadkarni G,
Kullo IJ,
Ritchie M,
Damrauer SM,
Tsao PS
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
Nielsen JB,
Fritsche LG,
Zhou W,
Teslovich TM,
Holmen OL,
Gustafsson S,
Gabrielsen ME,
Schmidt EM,
Beaumont R,
Wolford BN,
Lin M,
Brummett CM
and 33 more — show all
Preuss MH,
Refsgaard L,
Bottinger EP,
Graham SE,
Surakka I,
Chu Y,
Skogholt AH,
Dalen H,
Boyle AP,
Oral H,
Herron TJ,
Kitzman J,
Jalife J,
Svendsen JH,
Olesen MS,
Njølstad I,
Løchen ML,
Baras A,
Gottesman O,
Marcketta A,
O'Dushlaine C,
Ritchie MD,
Wilsgaard T,
Loos RJF,
Frayling TM,
Boehnke M,
Ingelsson E,
Carey DJ,
Dewey FE,
Kang HM,
Abecasis GR,
Hveem K,
Willer CJ
American journal of human genetics · 2018 · PMID 29290336
4 pages
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries
Surakka I,
Wu KH,
Hornsby W,
Wolford BN,
Shen F,
Zhou W,
Huffman JE,
Pandit A,
Hu Y,
Brumpton B,
Skogholt AH,
Gabrielsen ME
and 9 more — show all
TOPMed Stroke Working Group · Million Veteran Program (MVP) and 1 more consortia
Cell genomics · 2023 · PMID 37601974 · open access
2 pages
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
Zhou W,
Nielsen JB,
Fritsche LG,
Dey R,
Gabrielsen ME,
Wolford BN,
LeFaive J,
VandeHaar P,
Gagliano SA,
Gifford A,
Bastarache LA,
Wei WQ
and 7 more — show all
Nature genetics · 2018 · PMID 30104761 · open access
1 page
Genome-wide association study of cardiac troponin I in the general population
Moksnes MR,
Røsjø H,
Richmond A,
Lyngbakken MN,
Graham SE,
Hansen AF,
Wolford BN,
Gagliano Taliun SA,
LeFaive J,
Rasheed H,
Thomas LF,
Zhou W
and 18 more — show all
Aung N,
Surakka I,
Douville NJ,
Campbell A,
Porteous DJ,
Petersen SE,
Munroe PB,
Welsh P,
Sattar N,
Smith GD,
Fritsche LG,
Nielsen JB,
Åsvold BO,
Hveem K,
Hayward C,
Willer CJ,
Brumpton BM,
Omland T
Human molecular genetics · 2021 · PMID 33961016 · 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.