For researchers
Is your paper here?
2,657 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.
4 matches for
Rosen J.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen MH,
Raffield LM,
Mousas A,
Sakaue S,
Huffman JE,
Moscati A,
Trivedi B,
Jiang T,
Akbari P,
Vuckovic D,
Bao EL,
Zhong X
and 98 more — show all
Manansala R,
Laplante V,
Chen M,
Lo KS,
Qian H,
Lareau CA,
Beaudoin M,
Hunt KA,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala K,
Cho K,
Choquet H,
Correa A,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang QQ,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Lerch MM,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Martin HC,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nauck M,
Nikus K,
Ouwehand WH,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Roberts DJ,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Trembath RC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Zonderman AB,
Wilson PWF,
Li Y,
Butterworth AS,
Gauchat JF,
Chiang CWK,
Li B,
Loos RJF,
Astle WJ,
Evangelou E,
van Heel DA,
Sankaran VG,
Okada Y,
Soranzo N,
Johnson AD,
Reiner AP,
Auer PL,
Lettre G
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
The Polygenic and Monogenic Basis of Blood Traits and Diseases
Vuckovic D,
Bao EL,
Akbari P,
Lareau CA,
Mousas A,
Jiang T,
Chen MH,
Raffield LM,
Tardaguila M,
Huffman JE,
Ritchie SC,
Megy K
and 100 more — show all
Ponstingl H,
Penkett CJ,
Albers PK,
Wigdor EM,
Sakaue S,
Moscati A,
Manansala R,
Lo KS,
Qian H,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala KN,
Wilson PWF,
Choquet H,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Felix SB,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Guo Q,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nikus K,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Weiss S,
Cai N,
Kundu K,
Watt SB,
Walter K,
Zonderman AB,
Cho K,
Li Y,
Loos RJF,
Knight JC,
Georges M,
Stegle O,
Evangelou E,
Okada Y,
Roberts DJ,
Inouye M,
Johnson AD,
Auer PL,
Astle WJ,
Reiner AP,
Butterworth AS,
Ouwehand WH,
Lettre G,
Sankaran VG,
Soranzo N
VA Million Veteran Program
Cell · 2020 · PMID 32888494 · open access
12 pages+
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
and 66 more — show all
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Mikhaylova AV,
McHugh CP,
Polfus LM,
Raffield LM,
Boorgula MP,
Blackwell TW,
Brody JA,
Broome J,
Chami N,
Chen MH,
Conomos MP,
Cox C
and 81 more — show all
Curran JE,
Daya M,
Ekunwe L,
Glahn DC,
Heard-Costa N,
Highland HM,
Hobbs BD,
Ilboudo Y,
Jain D,
Lange LA,
Miller-Fleming TW,
Min N,
Moon JY,
Preuss MH,
Rosen J,
Ryan K,
Smith AV,
Sun Q,
Surendran P,
de Vries PS,
Walter K,
Wang Z,
Wheeler M,
Yanek LR,
Zhong X,
Abecasis GR,
Almasy L,
Barnes KC,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Chavan S,
Cho MH,
Choquet H,
Correa A,
Cox N,
DeMeo DL,
Faraday N,
Fornage M,
Gerszten RE,
Hou L,
Johnson AD,
Jorgenson E,
Kaplan R,
Kooperberg C,
Kundu K,
Laurie CA,
Lettre G,
Lewis JP,
Li B,
Li Y,
Lloyd-Jones DM,
Loos RJF,
Manichaikul A,
Meyers DA,
Mitchell BD,
Morrison AC,
Ngo D,
Nickerson DA,
Nongmaithem S,
North KE,
O'Connell JR,
Ortega VE,
Pankratz N,
Perry JA,
Psaty BM,
Rich SS,
Soranzo N,
Rotter JI,
Silverman EK,
Smith NL,
Tang H,
Tracy RP,
Thornton TA,
Vasan RS,
Zein J,
Mathias RA,
Reiner AP,
Auer PL
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
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.