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Is your paper here?
2,662 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
Schmidt F.
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Day FR,
Ruth KS,
Thompson DJ,
Lunetta KL,
Pervjakova N,
Chasman DI,
Stolk L,
Finucane HK,
Sulem P,
Bulik-Sullivan B,
Esko T,
Johnson AD
and 230 more — show all
Elks CE,
Franceschini N,
He C,
Altmaier E,
Brody JA,
Franke LL,
Huffman JE,
Keller MF,
McArdle PF,
Nutile T,
Porcu E,
Robino A,
Rose LM,
Schick UM,
Smith JA,
Teumer A,
Traglia M,
Vuckovic D,
Yao J,
Zhao W,
Albrecht E,
Amin N,
Corre T,
Hottenga JJ,
Mangino M,
Smith AV,
Tanaka T,
Abecasis G,
Andrulis IL,
Anton-Culver H,
Antoniou AC,
Arndt V,
Arnold AM,
Barbieri C,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernstein L,
Bielinski SJ,
Blomqvist C,
Boerwinkle E,
Bogdanova NV,
Bojesen SE,
Bolla MK,
Borresen-Dale AL,
Boutin TS,
Brauch H,
Brenner H,
Brüning T,
Burwinkel B,
Campbell A,
Campbell H,
Chanock SJ,
Chapman JR,
Chen YI,
Chenevix-Trench G,
Couch FJ,
Coviello AD,
Cox A,
Czene K,
Darabi H,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dörk T,
Dos-Santos-Silva I,
Dunning AM,
Eicher JD,
Fasching PA,
Faul JD,
Figueroa J,
Flesch-Janys D,
Gandin I,
Garcia ME,
García-Closas M,
Giles GG,
Girotto GG,
Goldberg MS,
González-Neira A,
Goodarzi MO,
Grove ML,
Gudbjartsson DF,
Guénel P,
Guo X,
Haiman CA,
Hall P,
Hamann U,
Henderson BE,
Hocking LJ,
Hofman A,
Homuth G,
Hooning MJ,
Hopper JL,
Hu FB,
Huang J,
Humphreys K,
Hunter DJ,
Jakubowska A,
Jones SE,
Kabisch M,
Karasik D,
Knight JA,
Kolcic I,
Kooperberg C,
Kosma VM,
Kriebel J,
Kristensen V,
Lambrechts D,
Langenberg C,
Li J,
Li X,
Lindström S,
Liu Y,
Luan J,
Lubinski J,
Mägi R,
Mannermaa A,
Manz J,
Margolin S,
Marten J,
Martin NG,
Masciullo C,
Meindl A,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Müller-Nurasyid M,
Nalls M,
Neale BM,
Nevanlinna H,
Neven P,
Newman AB,
Nordestgaard BG,
Olson JE,
Padmanabhan S,
Peterlongo P,
Peters U,
Petersmann A,
Peto J,
Pharoah PDP,
Pirastu NN,
Pirie A,
Pistis G,
Polasek O,
Porteous D,
Psaty BM,
Pylkäs K,
Radice P,
Raffel LJ,
Rivadeneira F,
Rudan I,
Rudolph A,
Ruggiero D,
Sala CF,
Sanna S,
Sawyer EJ,
Schlessinger D,
Schmidt MK,
Schmidt F,
Schmutzler RK,
Schoemaker MJ,
Scott RA,
Seynaeve CM,
Simard J,
Sorice R,
Southey MC,
Stöckl D,
Strauch K,
Swerdlow A,
Taylor KD,
Thorsteinsdottir U,
Toland AE,
Tomlinson I,
Truong T,
Tryggvadottir L,
Turner ST,
Vozzi D,
Wang Q,
Wellons M,
Willemsen G,
Wilson JF,
Winqvist R,
Wolffenbuttel BBHR,
Wright AF,
Yannoukakos D,
Zemunik T,
Zheng W,
Zheng W,
Zygmunt M,
Bergmann S,
Boomsma DI,
Buring JE,
Ferrucci L,
Montgomery GW,
Gudnason V,
Spector TD,
van Duijn CM,
Alizadeh BZ,
Ciullo M,
Crisponi L,
Easton DF,
Gasparini PP,
Gieger C,
Harris TB,
Hayward C,
Kardia SLR,
Kraft P,
McKnight B,
Metspalu A,
Morrison AC,
Reiner AP,
Ridker PM,
Rotter JI,
Toniolo D,
Uitterlinden AG,
Ulivi S,
Völzke H,
Wareham NJ,
Weir DR,
Yerges-Armstrong LM,
Price AL,
Stefansson K,
Visser JA,
Ong KK,
Chang-Claude J,
Murabito JM,
Perry JRB,
Murray A
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations
Thareja G,
Belkadi A,
Arnold M,
Albagha OME,
Graumann J,
Schmidt F,
Grallert H,
Peters A,
Gieger C,
Consortium TQGPR,
Suhre K
Human molecular genetics · 2023 · PMID 36168886 · open access
12 pages+
A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform
Suhre K,
Chen Q,
Halama A,
Mendez K,
Dahlin A,
Stephan N,
Thareja G,
Sarwath H,
Guturu H,
Dwaraka VB,
Smith R,
Batzoglou S
and 2 more — show all
Nature genetics · 2025 · PMID 41310232 · open access
12 pages+
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
Li R,
Brockschmidt FF,
Kiefer AK,
Stefansson H,
Nyholt DR,
Song K,
Vermeulen SH,
Kanoni S,
Glass D,
Medland SE,
Dimitriou M,
Waterworth D
and 27 more — show all
Tung JY,
Geller F,
Heilmann S,
Hillmer AM,
Bataille V,
Eigelshoven S,
Hanneken S,
Moebus S,
Herold C,
den Heijer M,
Montgomery GW,
Deloukas P,
Eriksson N,
Heath AC,
Becker T,
Sulem P,
Mangino M,
Vollenweider P,
Spector TD,
Dedoussis G,
Martin NG,
Kiemeney LA,
Mooser V,
Stefansson K,
Hinds DA,
Nöthen MM,
Richards JB
PLoS genetics · 2012 · PMID 22693459 · open access
3 pages
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
Hillmer AM,
Hanneken S,
Ritzmann S,
Becker T,
Freudenberg J,
Brockschmidt FF,
Flaquer A,
Freudenberg-Hua Y,
Jamra RA,
Metzen C,
Heyn U,
Schweiger N
and 13 more — show all
Betz RC,
Blaumeiser B,
Hampe J,
Schreiber S,
Schulze TG,
Hennies HC,
Schumacher J,
Propping P,
Ruzicka T,
Cichon S,
Wienker TF,
Kruse R,
Nothen MM
American journal of human genetics · 2005 · PMID 15902657
1 page
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children
Roeske D,
Ludwig KU,
Neuhoff N,
Becker J,
Bartling J,
Bruder J,
Brockschmidt FF,
Warnke A,
Remschmidt H,
Hoffmann P,
Müller-Myhsok B,
Nöthen MM
and 1 more — show all
Molecular psychiatry · 2011 · PMID 19786962
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.