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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.
6 matches for
Huntsman S.
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Paternoster L,
Standl M,
Waage J,
Baurecht H,
Hotze M,
Strachan DP,
Curtin JA,
Bønnelykke K,
Tian C,
Takahashi A,
Esparza-Gordillo J,
Alves AC
and 140 more — show all
Thyssen JP,
den Dekker HT,
Ferreira MA,
Altmaier E,
Sleiman PM,
Xiao FL,
Gonzalez JR,
Marenholz I,
Kalb B,
Yanes MP,
Xu CJ,
Carstensen L,
Groen-Blokhuis MM,
Venturini C,
Pennell CE,
Barton SJ,
Levin AM,
Curjuric I,
Bustamante M,
Kreiner-Møller E,
Lockett GA,
Bacelis J,
Bacelis J,
Bunyavanich S,
Myers RA,
Matanovic A,
Kumar A,
Tung JY,
Hirota T,
Kubo M,
McArdle WL,
Henderson AJ,
Kemp JP,
Zheng J,
Smith GD,
Rüschendorf F,
Bauerfeind A,
Lee-Kirsch MA,
Arnold A,
Homuth G,
Schmidt CO,
Mangold E,
Cichon S,
Keil T,
Rodríguez E,
Peters A,
Peters A,
Franke A,
Lieb W,
Novak N,
Fölster-Holst R,
Horikoshi M,
Pekkanen J,
Sebert S,
Husemoen LL,
Grarup N,
de Jongste JC,
Rivadeneira F,
Hofman A,
Jaddoe VW,
Pasmans SG,
Elbert NJ,
Uitterlinden AG,
Marks GB,
Thompson PJ,
Matheson MC,
Robertson CF,
Ried JS,
Li J,
Zuo XB,
Zheng XD,
Yin XY,
Sun LD,
McAleer MA,
O'Regan GM,
Fahy CM,
Campbell LE,
Macek M,
Kurek M,
Hu D,
Eng C,
Postma DS,
Feenstra B,
Geller F,
Hottenga JJ,
Middeldorp CM,
Hysi P,
Bataille V,
Spector T,
Tiesler CM,
Thiering E,
Pahukasahasram B,
Yang JJ,
Imboden M,
Huntsman S,
Vilor-Tejedor N,
Relton CL,
Myhre R,
Nystad W,
Custovic A,
Weiss ST,
Meyers DA,
Söderhäll C,
Melén E,
Ober C,
Raby BA,
Simpson A,
Jacobsson B,
Holloway JW,
Bisgaard H,
Sunyer J,
Hensch NMP,
Williams LK,
Godfrey KM,
Wang CA,
Boomsma DI,
Melbye M,
Koppelman GH,
Jarvis D,
McLean WI,
Irvine AD,
Zhang XJ,
Hakonarson H,
Gieger C,
Burchard EG,
Martin NG,
Duijts L,
Linneberg A,
Jarvelin MR,
Noethen MM,
Lau S,
Hübner N,
Lee YA,
Tamari M,
Hinds DA,
Glass D,
Brown SJ,
Heinrich J,
Evans DM,
Weidinger S
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations
Lona-Durazo F,
Hernandez-Pacheco N,
Fan S,
Zhang T,
Choi J,
Kovacs MA,
Loftus SK,
Le P,
Edwards M,
Fortes-Lima CA,
Fortes-Lima CA,
Eng C
and 15 more — show all
Huntsman S,
Hu D,
Gómez-Cabezas EJ,
Marín-Padrón LC,
Grauholm J,
Mors O,
Burchard EG,
Norton HL,
Pavan WJ,
Brown KM,
Tishkoff S,
Pino-Yanes M,
Beleza S,
Marcheco-Teruel B,
Parra EJ
BMC genetics · 2019 · PMID 31315583 · open access
3 pages
A meta-analysis of genome-wide association studies of asthma in Puerto Ricans
Yan Q,
Brehm J,
Pino-Yanes M,
Forno E,
Lin J,
Oh SS,
Acosta-Perez E,
Laurie CC,
Cloutier MM,
Raby BA,
Stilp AM,
Sofer T
and 11 more — show all
Hu D,
Huntsman S,
Eng CS,
Conomos MP,
Rastogi D,
Rice K,
Canino G,
Chen W,
Barr RG,
Burchard EG,
Celedón JC
The European respiratory journal · 2017 · PMID 28461288
2 pages
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Siddiq A,
Couch FJ,
Chen GK,
Lindström S,
Eccles D,
Millikan RC,
Michailidou K,
Stram DO,
Beckmann L,
Rhie SK,
Ambrosone CB,
Aittomäki K
and 129 more — show all
Amiano P,
Apicella C,
Baglietto L,
Bandera EV,
Beckmann MW,
Berg CD,
Bernstein L,
Blomqvist C,
Brauch H,
Brinton L,
Bui QM,
Buring JE,
Buys SS,
Campa D,
Carpenter JE,
Chasman DI,
Chang-Claude J,
Chen C,
Clavel-Chapelon F,
Cox A,
Cross SS,
Czene K,
Deming SL,
Diasio RB,
Diver WR,
Dunning AM,
Durcan L,
Ekici AB,
Fasching PA,
Feigelson HS,
Fejerman L,
Figueroa JD,
Fletcher O,
Flesch-Janys D,
Gaudet MM,
Gerty SM,
Rodriguez-Gil JL,
Giles GG,
van Gils CH,
Godwin AK,
Graham N,
Greco D,
Hall P,
Hankinson SE,
Hartmann A,
Hein R,
Heinz J,
Hoover RN,
Hopper JL,
Hu JJ,
Huntsman S,
Ingles SA,
Irwanto A,
Isaacs C,
Jacobs KB,
John EM,
Justenhoven C,
Kaaks R,
Kolonel LN,
Coetzee GA,
Lathrop M,
Le Marchand L,
Lee AM,
Lee IM,
Lesnick T,
Lichtner P,
Liu J,
Lund E,
Makalic E,
Martin NG,
McLean CA,
Meijers-Heijboer H,
Meindl A,
Miron P,
Monroe KR,
Montgomery GW,
Müller-Myhsok B,
Nickels S,
Nyante SJ,
Olswold C,
Overvad K,
Palli D,
Park DJ,
Palmer JR,
Pathak H,
Peto J,
Pharoah P,
Rahman N,
Rivadeneira F,
Schmidt DF,
Schmutzler RK,
Slager S,
Southey MC,
Stevens KN,
Sinn HP,
Press MF,
Ross E,
Riboli E,
Ridker PM,
Schumacher FR,
Severi G,
Dos Santos Silva I,
Stone J,
Sund M,
Tapper WJ,
Thun MJ,
Travis RC,
Turnbull C,
Uitterlinden AG,
Waisfisz Q,
Wang X,
Wang Z,
Weaver J,
Schulz-Wendtland R,
Wilkens LR,
Van Den Berg D,
Zheng W,
Zheng W,
Ziegler RG,
Ziv E,
Nevanlinna H,
Easton DF,
Hunter DJ,
Henderson BE,
Chanock SJ,
Garcia-Closas M,
Kraft P,
Haiman CA,
Vachon CM
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study and 1 more consortia
Human molecular genetics · 2012 · PMID 22976474
1 page
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25
Fejerman L,
Ahmadiyeh N,
Hu D,
Huntsman S,
Beckman KB,
Caswell JL,
Tsung K,
John EM,
Torres-Mejia G,
Carvajal-Carmona L,
Echeverry MM,
Tuazon AM
and 14 more — show all
Ramirez C,
Gignoux CR,
Eng C,
Gonzalez-Burchard E,
Henderson B,
Le Marchand L,
Kooperberg C,
Hou L,
Agalliu I,
Kraft P,
Lindström S,
Perez-Stable EJ,
Haiman CA,
Ziv E
COLUMBUS Consortium
Nature communications · 2014 · PMID 25327703 · open access
1 page
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients
Ziv E,
Dean E,
Hu D,
Martino A,
Serie D,
Curtin K,
Campa D,
Aftab B,
Bracci P,
Buda G,
Zhao Y,
Caswell-Jin J
and 27 more — show all
Diasio R,
Dumontet C,
Dudziński M,
Fejerman L,
Greenberg A,
Huntsman S,
Jamroziak K,
Jurczyszyn A,
Kumar S,
Atanackovic D,
Glenn M,
Cannon-Albright LA,
Jones B,
Lee A,
Marques H,
Martin T,
Martinez-Lopez J,
Martinez-Lopez J,
Rajkumar V,
Sainz J,
Vangsted AJ,
Wątek M,
Wolf J,
Slager S,
Camp NJ,
Canzian F,
Vachon C
Nature communications · 2015 · PMID 26198393
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.