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2,663 papers hold this site up. Every variant and condition page names
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11 matches for
Germain M.
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+
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
Sabater-Lleal M,
Huffman JE,
de Vries PS,
Marten J,
Mastrangelo MA,
Song C,
Pankratz N,
Ward-Caviness CK,
Yanek LR,
Trompet S,
Delgado GE,
Guo X
and 64 more — show all
Bartz TM,
Martinez-Perez A,
Germain M,
de Haan HG,
Ozel AB,
Polasek O,
Smith AV,
Eicher JD,
Reiner AP,
Tang W,
Davies NM,
Stott DJ,
Rotter JI,
Tofler GH,
Boerwinkle E,
de Maat MPM,
Kleber ME,
Welsh P,
Brody JA,
Chen MH,
Vaidya D,
Soria JM,
Suchon P,
van Hylckama Vlieg A,
Desch KC,
Kolcic I,
Joshi PK,
Launer LJ,
Harris TB,
Campbell H,
Rudan I,
Becker DM,
Li JZ,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
Franco OH,
Cushman M,
Psaty BM,
Morange PE,
McKnight B,
Chong MR,
Fernandez-Cadenas I,
Rosand J,
Lindgren A,
Gudnason V,
Wilson JF,
Hayward C,
Ginsburg D,
Fornage M,
Rosendaal FR,
Souto JC,
Becker LC,
Jenny NS,
März W,
Jukema JW,
Dehghan A,
Trégouët DA,
Morrison AC,
Johnson AD,
O'Donnell CJ,
Strachan DP,
Lowenstein CJ,
Smith NL
INVENT Consortium; MEGASTROKE Consortium of the International Stroke Genetics Consortium (ISGC)
Circulation · 2019 · PMID 30586737
8 pages
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
Rhodes CJ,
Batai K,
Bleda M,
Haimel M,
Southgate L,
Germain M,
Pauciulo MW,
Hadinnapola C,
Aman J,
Girerd B,
Arora A,
Knight J
and 106 more — show all
Hanscombe KB,
Karnes JH,
Kaakinen M,
Gall H,
Ulrich A,
Harbaum L,
Cebola I,
Ferrer J,
Lutz K,
Swietlik EM,
Ahmad F,
Amouyel P,
Archer SL,
Argula R,
Austin ED,
Badesch D,
Bakshi S,
Barnett C,
Benza R,
Bhatt N,
Bogaard HJ,
Burger CD,
Chakinala M,
Church C,
Coghlan JG,
Condliffe R,
Corris PA,
Danesino C,
Debette S,
Elliott CG,
Elwing J,
Eyries M,
Fortin T,
Franke A,
Frantz RP,
Frost A,
Garcia JGN,
Ghio S,
Ghofrani HA,
Gibbs JSR,
Harley J,
He H,
Hill NS,
Hirsch R,
Houweling AC,
Howard LS,
Ivy D,
Kiely DG,
Klinger J,
Kovacs G,
Lahm T,
Laudes M,
Machado RD,
MacKenzie Ross RV,
Marsolo K,
Martin LJ,
Moledina S,
Montani D,
Nathan SD,
Newnham M,
Olschewski A,
Olschewski H,
Oudiz RJ,
Ouwehand WH,
Peacock AJ,
Pepke-Zaba J,
Rehman Z,
Robbins I,
Roden DM,
Rosenzweig EB,
Saydain G,
Scelsi L,
Schilz R,
Seeger W,
Shaffer CM,
Simms RW,
Simon M,
Sitbon O,
Suntharalingam J,
Tang H,
Tchourbanov AY,
Thenappan T,
Torres F,
Toshner MR,
Treacy CM,
Vonk Noordegraaf A,
Waisfisz Q,
Walsworth AK,
Walter RE,
Wharton J,
White RJ,
Wilt J,
Wort SJ,
Yung D,
Lawrie A,
Humbert M,
Soubrier F,
Trégouët DA,
Prokopenko I,
Kittles R,
Gräf S,
Nichols WC,
Trembath RC,
Desai AA,
Morrell NW,
Wilkins MR
UK NIHR BioResource Rare Diseases Consortium · UK PAH Cohort Study Consortium and 1 more consortia
The Lancet. Respiratory medicine · 2019 · PMID 30527956 · open access
4 pages
Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes
Munsch G,
Thibord F,
Bezerra OC,
Brody JA,
van Hylckama Vlieg A,
Gourhant L,
Chen MH,
Samaria F,
Germain M,
Caro I,
Suchon P,
Olaso R
and 22 more — show all
Wiggins KL,
Saut N,
Besse C,
Goumidi L,
Bacq D,
Harrington LB,
Boland A,
Emmerich J,
Smadja DM,
Lemarié CA,
Danckwardt S,
Debette S,
Deleuze JF,
Jacqmin-Gadda H,
Rodger MA,
Gagnon F,
Rosendaal FR,
Johnson AD,
Smith NL,
Couturaud F,
Morange PE,
Trégouët DA
Blood · 2025 · PMID 40811855
4 pages
Genetics of venous thrombosis: insights from a new genome wide association study
Germain M,
Saut N,
Greliche N,
Dina C,
Lambert JC,
Perret C,
Cohen W,
Oudot-Mellakh T,
Antoni G,
Alessi MC,
Zelenika D,
Cambien F
and 9 more — show all
PloS one · 2011 · PMID 21980494 · open access
2 pages
A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential
Rocanin-Arjo A,
Cohen W,
Carcaillon L,
Frère C,
Saut N,
Letenneur L,
Alhenc-Gelas M,
Dupuy AM,
Bertrand M,
Alessi MC,
Germain M,
Wild PS
and 7 more — show all
CardioGenics Consortium
Blood · 2014 · PMID 24357727
2 pages
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis
Hinds DA,
Buil A,
Ziemek D,
Martinez-Perez A,
Malik R,
Folkersen L,
Germain M,
Mälarstig A,
Brown A,
Soria JM,
Dichgans M,
Bing N
and 7 more — show all
METASTROKE Consortium, INVENT Consortium
Human molecular genetics · 2016 · PMID 26908601
2 pages
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism
Lindström S,
Wang L,
Smith EN,
Gordon W,
van Hylckama Vlieg A,
de Andrade M,
Brody JA,
Pattee JW,
Haessler J,
Brumpton BM,
Chasman DI,
Suchon P
and 45 more — show all
Chen MH,
Turman C,
Germain M,
Wiggins KL,
MacDonald J,
Braekkan SK,
Armasu SM,
Pankratz N,
Jackson RD,
Nielsen JB,
Giulianini F,
Puurunen MK,
Ibrahim M,
Heckbert SR,
Damrauer SM,
Natarajan P,
Klarin D,
de Vries PS,
Sabater-Lleal M,
Huffman JE,
Bammler TK,
Frazer KA,
McCauley BM,
Taylor K,
Pankow JS,
Reiner AP,
Gabrielsen ME,
Deleuze JF,
O'Donnell CJ,
Kim J,
McKnight B,
Kraft P,
Hansen JB,
Rosendaal FR,
Heit JA,
Psaty BM,
Tang W,
Kooperberg C,
Hveem K,
Ridker PM,
Morange PE,
Johnson AD,
Kabrhel C,
Trégouët DA,
Smith NL
Million Veteran Program · CHARGE Hemostasis Working Group
Blood · 2019 · PMID 31420334
2 pages
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
Garnier S,
Harakalova M,
Weiss S,
Mokry M,
Regitz-Zagrosek V,
Hengstenberg C,
Cappola TP,
Isnard R,
Arbustini E,
Cook SA,
van Setten J,
Calis JJA
and 64 more — show all
Hakonarson H,
Morley MP,
Stark K,
Prasad SK,
Li J,
O'Regan DP,
Grasso M,
Müller-Nurasyid M,
Meitinger T,
Empana JP,
Strauch K,
Waldenberger M,
Marguiles KB,
Seidman CE,
Kararigas G,
Meder B,
Haas J,
Boutouyrie P,
Lacolley P,
Jouven X,
Erdmann J,
Blankenberg S,
Wichter T,
Ruppert V,
Tavazzi L,
Dubourg O,
Roizes G,
Dorent R,
de Groote P,
Fauchier L,
Trochu JN,
Aupetit JF,
Bilinska ZT,
Germain M,
Völker U,
Hemerich D,
Raji I,
Bacq-Daian D,
Proust C,
Remior P,
Gomez-Bueno M,
Lehnert K,
Maas R,
Olaso R,
Saripella GV,
Felix SB,
McGinn S,
Duboscq-Bidot L,
van Mil A,
Besse C,
Fontaine V,
Blanché H,
Ader F,
Keating B,
Curjol A,
Boland A,
Komajda M,
Cambien F,
Deleuze JF,
Dörr M,
Asselbergs FW,
Villard E,
Trégouët DA,
Charron P
European heart journal · 2021 · PMID 33677556
2 pages
C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies
Buil A,
Trégouët DA,
Souto JC,
Saut N,
Germain M,
Rotival M,
Tiret L,
Cambien F,
Lathrop M,
Zeller T,
Alessi MC,
Rodriguez de Cordoba S
and 9 more — show all
Blood · 2010 · PMID 20212171
1 page
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Iglesias MJ,
Sanchez-Rivera L,
Ibrahim-Kosta M,
Naudin C,
Munsch G,
Goumidi L,
Farm M,
Smith PM,
Thibord F,
Kral-Pointner JB,
Hong MG,
Suchon P
and 31 more — show all
Germain M,
Schrottmaier W,
Dusart P,
Boland A,
Kotol D,
Edfors F,
Koprulu M,
Pietzner M,
Langenberg C,
Damrauer SM,
Johnson AD,
Klarin DM,
Smith NL,
Smadja DM,
Holmström M,
Magnusson M,
Silveira A,
Uhlén M,
Renné T,
Martinez-Perez A,
Emmerich J,
Deleuze JF,
Antovic J,
Soria Fernandez JM,
Assinger A,
Schwenk JM,
Souto Andres JC,
Morange PE,
Butler LM,
Trégouët DA,
Odeberg J
Nature communications · 2023 · PMID 37286573 · 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.