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2,663 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.
24 matches for
Hoffmann TJ,
showing the first 20.
A large electronic-health-record-based genome-wide study of serum lipids
Hoffmann TJ,
Theusch E,
Haldar T,
Ranatunga DK,
Jorgenson E,
Medina MW,
Kvale MN,
Kwok PY,
Schaefer C,
Krauss RM,
Iribarren C,
Risch N
Nature genetics · 2018 · PMID 29507422 · open access
12 pages+
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci
Choquet H,
Paylakhi S,
Kneeland SC,
Thai KK,
Hoffmann TJ,
Yin J,
Kvale MN,
Banda Y,
Tolman NG,
Williams PA,
Schaefer C,
Melles RB
and 4 more — show all
Nature communications · 2018 · PMID 29891935 · open access
12 pages+
Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts
Rashkin SR,
Graff RE,
Kachuri L,
Thai KK,
Alexeeff SE,
Blatchins MA,
Cavazos TB,
Corley DA,
Emami NC,
Hoffman JD,
Jorgenson E,
Kushi LH
and 7 more — show all
Nature communications · 2020 · PMID 32887889 · open access
12 pages+
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Conti DV,
Darst BF,
Moss LC,
Saunders EJ,
Sheng X,
Chou A,
Schumacher FR,
Olama AAA,
Benlloch S,
Dadaev T,
Brook MN,
Sahimi A
and 220 more — show all
Hoffmann TJ,
Takahashi A,
Matsuda K,
Momozawa Y,
Fujita M,
Muir K,
Lophatananon A,
Wan P,
Le Marchand L,
Wilkens LR,
Stevens VL,
Gapstur SM,
Carter BD,
Schleutker J,
Tammela TLJ,
Sipeky C,
Auvinen A,
Giles GG,
Southey MC,
MacInnis RJ,
Cybulski C,
Wokołorczyk D,
Lubiński J,
Neal DE,
Donovan JL,
Hamdy FC,
Martin RM,
Nordestgaard BG,
Nielsen SF,
Weischer M,
Bojesen SE,
Røder MA,
Iversen P,
Batra J,
Chambers S,
Moya L,
Horvath L,
Clements JA,
Tilley W,
Risbridger GP,
Gronberg H,
Aly M,
Szulkin R,
Eklund M,
Nordström T,
Pashayan N,
Dunning AM,
Ghoussaini M,
Travis RC,
Key TJ,
Riboli E,
Park JY,
Sellers TA,
Lin HY,
Albanes D,
Weinstein SJ,
Mucci LA,
Giovannucci E,
Lindstrom S,
Kraft P,
Hunter DJ,
Penney KL,
Turman C,
Tangen CM,
Goodman PJ,
Thompson IM Jr,
Hamilton RJ,
Fleshner NE,
Finelli A,
Parent MÉ,
Stanford JL,
Ostrander EA,
Geybels MS,
Koutros S,
Freeman LEB,
Stampfer M,
Wolk A,
Håkansson N,
Andriole GL,
Hoover RN,
Machiela MJ,
Sørensen KD,
Borre M,
Blot WJ,
Zheng W,
Zheng W,
Yeboah ED,
Mensah JE,
Lu YJ,
Zhang HW,
Feng N,
Mao X,
Wu Y,
Zhao SC,
Sun Z,
Thibodeau SN,
McDonnell SK,
Schaid DJ,
West CML,
Burnet N,
Barnett G,
Maier C,
Schnoeller T,
Luedeke M,
Kibel AS,
Drake BF,
Cussenot O,
Cancel-Tassin G,
Menegaux F,
Truong T,
Koudou YA,
John EM,
Grindedal EM,
Maehle L,
Khaw KT,
Ingles SA,
Stern MC,
Vega A,
Gómez-Caamaño A,
Fachal L,
Rosenstein BS,
Kerns SL,
Ostrer H,
Teixeira MR,
Paulo P,
Brandão A,
Watya S,
Lubwama A,
Bensen JT,
Fontham ETH,
Mohler J,
Taylor JA,
Kogevinas M,
Llorca J,
Castaño-Vinyals G,
Cannon-Albright L,
Teerlink CC,
Huff CD,
Strom SS,
Multigner L,
Blanchet P,
Brureau L,
Kaneva R,
Slavov C,
Mitev V,
Leach RJ,
Weaver B,
Brenner H,
Cuk K,
Holleczek B,
Saum KU,
Klein EA,
Hsing AW,
Kittles RA,
Murphy AB,
Logothetis CJ,
Kim J,
Neuhausen SL,
Steele L,
Ding YC,
Isaacs WB,
Nemesure B,
Hennis AJM,
Carpten J,
Pandha H,
Michael A,
De Ruyck K,
De Meerleer G,
Ost P,
Xu J,
Razack A,
Lim J,
Teo SH,
Newcomb LF,
Lin DW,
Fowke JH,
Neslund-Dudas C,
Rybicki BA,
Gamulin M,
Lessel D,
Kulis T,
Usmani N,
Singhal S,
Parliament M,
Claessens F,
Joniau S,
Van den Broeck T,
Gago-Dominguez M,
Castelao JE,
Martinez ME,
Larkin S,
Townsend PA,
Aukim-Hastie C,
Bush WS,
Aldrich MC,
Crawford DC,
Srivastava S,
Cullen JC,
Petrovics G,
Casey G,
Roobol MJ,
Jenster G,
van Schaik RHN,
Hu JJ,
Sanderson M,
Varma R,
McKean-Cowdin R,
Torres M,
Mancuso N,
Berndt SI,
Van Den Eeden SK,
Easton DF,
Chanock SJ,
Cook MB,
Wiklund F,
Nakagawa H,
Witte JS,
Eeles RA,
Kote-Jarai Z,
Haiman CA
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects
Choquet H,
Melles RB,
Anand D,
Yin J,
Cuellar-Partida G,
Wang W,
Hoffmann TJ,
Nair KS,
Hysi PG,
Lachke SA,
Jorgenson E
23andMe Research Team
Nature communications · 2021 · PMID 34127677 · open access
12 pages+
Genetically adjusted PSA levels for prostate cancer screening
Kachuri L,
Hoffmann TJ,
Jiang Y,
Berndt SI,
Shelley JP,
Schaffer KR,
Machiela MJ,
Freedman ND,
Huang WY,
Li SA,
Easterlin R,
Goodman PJ
and 11 more — show all
Till C,
Thompson I,
Lilja H,
Van Den Eeden SK,
Chanock SJ,
Haiman CA,
Conti DV,
Klein RJ,
Mosley JD,
Graff RE,
Witte JS
Nature medicine · 2023 · PMID 37264206 · open access
12 pages+
Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups
Hoffmann TJ,
Graff RE,
Madduri RK,
Rodriguez AA,
Cario CL,
Feng K,
Jiang Y,
Wang A,
Klein RJ,
Pierce BL,
Eggener S,
Tong L
and 37 more — show all
Blot W,
Long J,
Goss LB,
Darst BF,
Rebbeck T,
Lachance J,
Andrews C,
Adebiyi AO,
Adusei B,
Aisuodionoe-Shadrach OI,
Fernandez PW,
Jalloh M,
Janivara R,
Chen WC,
Mensah JE,
Agalliu I,
Berndt SI,
Shelley JP,
Schaffer K,
Machiela MJ,
Freedman ND,
Huang WY,
Li SA,
Goodman PJ,
Till C,
Thompson I,
Lilja H,
Ranatunga DK,
Presti J,
Van Den Eeden SK,
Chanock SJ,
Mosley JD,
Conti DV,
Haiman CA,
Justice AC,
Kachuri L,
Witte JS
Nature genetics · 2025 · PMID 39930085 · open access
12 pages+
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
Liu C,
Kraja AT,
Smith JA,
Brody JA,
Franceschini N,
Bis JC,
Rice K,
Morrison AC,
Lu Y,
Weiss S,
Guo X,
Palmas W
and 83 more — show all
Martin LW,
Chen YD,
Surendran P,
Drenos F,
Cook JP,
Auer PL,
Chu AY,
Giri A,
Zhao W,
Jakobsdottir J,
Lin LA,
Stafford JM,
Amin N,
Mei H,
Yao J,
Voorman A,
Larson MG,
Grove ML,
Smith AV,
Hwang SJ,
Chen H,
Huan T,
Kosova G,
Stitziel NO,
Kathiresan S,
Samani N,
Schunkert H,
Deloukas P,
Li M,
Fuchsberger C,
Pattaro C,
Gorski M,
Kooperberg C,
Papanicolaou GJ,
Rossouw JE,
Faul JD,
Kardia SL,
Bouchard C,
Raffel LJ,
Uitterlinden AG,
Franco OH,
Vasan RS,
O'Donnell CJ,
Taylor KD,
Liu K,
Bottinger EP,
Gottesman O,
Daw EW,
Giulianini F,
Ganesh S,
Salfati E,
Harris TB,
Launer LJ,
Dörr M,
Felix SB,
Rettig R,
Völzke H,
Kim E,
Lee WJ,
Lee IT,
Sheu WH,
Tsosie KS,
Edwards DR,
Liu Y,
Correa A,
Weir DR,
Völker U,
Ridker PM,
Boerwinkle E,
Gudnason V,
Reiner AP,
van Duijn CM,
Borecki IB,
Edwards TL,
Chakravarti A,
Rotter JI,
Psaty BM,
Loos RJ,
Fornage M,
Ehret GB,
Newton-Cheh C,
Levy D,
Chasman DI
CHD Exome+ Consortium · ExomeBP Consortium and 4 more consortia
Nature genetics · 2016 · PMID 27618448
9 pages
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations
Coram MA,
Duan Q,
Hoffmann TJ,
Thornton T,
Knowles JW,
Johnson NA,
Ochs-Balcom HM,
Donlon TA,
Martin LW,
Eaton CB,
Robinson JG,
Risch NJ
and 5 more — show all
American journal of human genetics · 2013 · PMID 23726366
5 pages
Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer
Hoffmann TJ,
Passarelli MN,
Graff RE,
Emami NC,
Sakoda LC,
Jorgenson E,
Habel LA,
Shan J,
Ranatunga DK,
Quesenberry CP,
Chao CR,
Ghai NR
and 17 more — show all
Aaronson D,
Presti J,
Nordström T,
Wang Z,
Berndt SI,
Chanock SJ,
Mosley JD,
Klein RJ,
Middha M,
Lilja H,
Melander O,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Van Den Eeden SK,
Witte JS
Nature communications · 2017 · PMID 28139693 · open access
5 pages
A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences
Hoffmann TJ,
Van Den Eeden SK,
Sakoda LC,
Jorgenson E,
Habel LA,
Graff RE,
Passarelli MN,
Cario CL,
Emami NC,
Chao CR,
Ghai NR,
Shan J
and 23 more — show all
Ranatunga DK,
Quesenberry CP,
Aaronson D,
Presti J,
Wang Z,
Berndt SI,
Chanock SJ,
McDonnell SK,
French AJ,
Schaid DJ,
Thibodeau SN,
Li Q,
Freedman ML,
Penney KL,
Mucci LA,
Haiman CA,
Henderson BE,
Seminara D,
Kvale MN,
Kwok PY,
Schaefer C,
Risch N,
Witte JS
Cancer discovery · 2015 · PMID 26034056
3 pages
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.