For researchers
Is your paper here?
2,673 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
Schurmann C,
showing the first 4.
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
Schick UM,
Jain D,
Hodonsky CJ,
Morrison JV,
Davis JP,
Brown L,
Sofer T,
Conomos MP,
Schurmann C,
McHugh CP,
Nelson SC,
Vadlamudi S
and 26 more — show all
Stilp A,
Plantinga A,
Baier L,
Bien SA,
Gogarten SM,
Laurie CA,
Taylor KD,
Liu Y,
Auer PL,
Franceschini N,
Szpiro A,
Rice K,
Kerr KF,
Rotter JI,
Hanson RL,
Papanicolaou G,
Rich SS,
Loos RJ,
Browning BL,
Browning SR,
Weir BS,
Laurie CC,
Mohlke KL,
North KE,
Thornton TA,
Reiner AP
American journal of human genetics · 2016 · PMID 26805783
1 page
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A<sub>1c</sub> With Implications for Glycemic Status in U.S. Hispanics/Latinos
Moon JY,
Louie TL,
Jain D,
Sofer T,
Schurmann C,
Below JE,
Lai CQ,
Aviles-Santa ML,
Talavera GA,
Smith CE,
Petty LE,
Bottinger EP
and 13 more — show all
Chen YI,
Taylor KD,
Daviglus ML,
Cai J,
Wang T,
Tucker KL,
Ordovás JM,
Hanis CL,
Loos RJF,
Schneiderman N,
Rotter JI,
Kaplan RC,
Qi Q
Diabetes care · 2019 · PMID 31213470
1 page
Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL,
Graff M,
Nishimura KK,
Tao R,
Haessler J,
Gignoux CR,
Highland HM,
Patel YM,
Sorokin EP,
Avery CL,
Belbin GM,
Bien SA
and 74 more — show all
Cheng I,
Cullina S,
Hodonsky CJ,
Hu Y,
Huckins LM,
Jeff J,
Justice AE,
Kocarnik JM,
Lim U,
Lin BM,
Lu Y,
Nelson SC,
Park SL,
Poisner H,
Preuss MH,
Richard MA,
Schurmann C,
Setiawan VW,
Sockell A,
Vahi K,
Verbanck M,
Vishnu A,
Walker RW,
Young KL,
Zubair N,
Acuña-Alonso V,
Ambite JL,
Barnes KC,
Boerwinkle E,
Bottinger EP,
Bustamante CD,
Caberto C,
Canizales-Quinteros S,
Conomos MP,
Deelman E,
Do R,
Doheny K,
Fernández-Rhodes L,
Fornage M,
Hailu B,
Heiss G,
Henn BM,
Hindorff LA,
Jackson RD,
Laurie CA,
Laurie CC,
Li Y,
Lin DY,
Moreno-Estrada A,
Nadkarni G,
Norman PJ,
Pooler LC,
Reiner AP,
Romm J,
Sabatti C,
Sandoval K,
Sheng X,
Stahl EA,
Stram DO,
Thornton TA,
Wassel CL,
Wilkens LR,
Winkler CA,
Yoneyama S,
Buyske S,
Haiman CA,
Kooperberg C,
Le Marchand L,
Loos RJF,
Matise TC,
North KE,
Peters U,
Kenny EE,
Carlson CS
Nature · 2019 · PMID 31217584
1 page
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
Yaghootkar H,
Zhang Y,
Spracklen CN,
Karaderi T,
Huang LO,
Bradfield J,
Schurmann C,
Fine RS,
Preuss MH,
Kutalik Z,
Wittemans LBL,
Lu Y
and 104 more — show all
Metz S,
Willems SM,
Li-Gao R,
Grarup N,
Wang S,
Molnos S,
Sandoval-Zárate AA,
Nalls MA,
Lange LA,
Haesser J,
Guo X,
Lyytikäinen LP,
Feitosa MF,
Sitlani CM,
Venturini C,
Mahajan A,
Kacprowski T,
Wang CA,
Chasman DI,
Amin N,
Broer L,
Robertson N,
Young KL,
Allison M,
Auer PL,
Blüher M,
Borja JB,
Bork-Jensen J,
Carrasquilla GD,
Christofidou P,
Demirkan A,
Doege CA,
Garcia ME,
Graff M,
Guo K,
Hakonarson H,
Hong J,
Ida Chen YD,
Jackson R,
Jakupović H,
Jousilahti P,
Justice AE,
Kähönen M,
Kizer JR,
Kriebel J,
LeDuc CA,
Li J,
Lind L,
Luan J,
Mackey DA,
Mangino M,
Männistö S,
Martin Carli JF,
Medina-Gomez C,
Mook-Kanamori DO,
Morris AP,
de Mutsert R,
Nauck M,
Prokic I,
Pennell CE,
Pradhan AD,
Psaty BM,
Raitakari OT,
Scott RA,
Skaaby T,
Strauch K,
Taylor KD,
Teumer A,
Uitterlinden AG,
Wu Y,
Yao J,
Walker M,
North KE,
Kovacs P,
Ikram MA,
van Duijn CM,
Ridker PM,
Lye S,
Homuth G,
Ingelsson E,
Spector TD,
McKnight B,
Province MA,
Lehtimäki T,
Adair LS,
Rotter JI,
Reiner AP,
Wilson JG,
Harris TB,
Ripatti S,
Grallert H,
Meigs JB,
Salomaa V,
Hansen T,
Willems van Dijk K,
Wareham NJ,
Grant SFA,
Langenberg C,
Frayling TM,
Lindgren CM,
Mohlke KL,
Leibel RL,
Loos RJF,
Kilpeläinen TO
Diabetes · 2020 · PMID 32917775
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.