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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.
6 matches for
Houlden H.
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls MA,
Pankratz N,
Lill CM,
Do CB,
Hernandez DG,
Saad M,
DeStefano AL,
Kara E,
Bras J,
Sharma M,
Schulte C,
Keller MF
and 35 more — show all
Arepalli S,
Letson C,
Edsall C,
Stefansson H,
Liu X,
Pliner H,
Lee JH,
Cheng R,
Ikram MA,
Ioannidis JP,
Hadjigeorgiou GM,
Bis JC,
Martinez M,
Perlmutter JS,
Goate A,
Marder K,
Fiske B,
Sutherland M,
Xiromerisiou G,
Myers RH,
Clark LN,
Stefansson K,
Hardy JA,
Heutink P,
Chen H,
Wood NW,
Houlden H,
Payami H,
Brice A,
Scott WK,
Gasser T,
Bertram L,
Eriksson N,
Foroud T,
Singleton AB
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and 10 more consortia
Nature genetics · 2014 · PMID 25064009 · open access
12 pages+
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
and 121 more — show all
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
Sliz E,
Sobalska-Kwapis M,
Thorleifsson G,
Topbas-Selcuki NF,
Vitonis A,
Westergaard D,
Arnadottir R,
Burgdorf KS,
Campbell A,
Cheuk CSK,
Clementi C,
Cook J,
De Vivo I,
DiVasta A,
Dorien O,
Donoghue JF,
Edwards T,
Fontanillas P,
Fung JN,
Geirsson RT,
Girling JE,
Harkki P,
Harris HR,
Healey M,
Heikinheimo O,
Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
Jarvelin MR,
Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
Laivuori H,
Laufer MR,
Lindgren CM,
MacGregor S,
Mangino M,
Martin NG,
Matalliotaki C,
Matalliotakis M,
Murray AD,
Ndungu A,
Nezhat C,
Olsen CM,
Opoku-Anane J,
Padmanabhan S,
Paranjpe M,
Peters M,
Polak G,
Porteous DJ,
Rabban J,
Rexrode KM,
Romanowicz H,
Saare M,
Saavalainen L,
Schork AJ,
Sen S,
Shafrir AL,
Siewierska-Górska A,
Słomka M,
Smith BH,
Smolarz B,
Szaflik T,
Szyłło K,
Takahashi A,
Terry KL,
Tomassetti C,
Treloar SA,
Vanhie A,
Vincent K,
Vo KC,
Werring DJ,
Zeggini E,
Zervou MI,
Adachi S,
Buring JE,
Ridker PM,
D'Hooghe T,
Goulielmos GN,
Hapangama DK,
Hayward C,
Horne AW,
Low SK,
Martikainen H,
Chasman DI,
Rogers PAW,
Saunders PT,
Sirota M,
Spector T,
Strapagiel D,
Tung JY,
Whiteman DC,
Giudice LC,
Velez-Edwards DR,
Uimari O,
Kraft P,
Salumets A,
Nyholt DR,
Mägi R,
Stefansson K,
Becker CM,
Yurttas-Beim P,
Steinthorsdottir V,
Nyegaard M,
Missmer SA,
Montgomery GW,
Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Bakker MK,
van der Spek RAA,
van Rheenen W,
Morel S,
Bourcier R,
Hostettler IC,
Alg VS,
van Eijk KR,
Koido M,
Akiyama M,
Terao C,
Matsuda K
and 62 more — show all
Walters RG,
Lin K,
Li L,
Millwood IY,
Chen Z,
Rouleau GA,
Zhou S,
Rannikmäe K,
Sudlow CLM,
Houlden H,
van den Berg LH,
Dina C,
Naggara O,
Gentric JC,
Shotar E,
Eugène F,
Desal H,
Winsvold BS,
Børte S,
Johnsen MB,
Brumpton BM,
Sandvei MS,
Willer CJ,
Hveem K,
Zwart JA,
Verschuren WMM,
Friedrich CM,
Hirsch S,
Schilling S,
Dauvillier J,
Martin O,
Jones GT,
Bown MJ,
Ko NU,
Kim H,
Coleman JRI,
Breen G,
Zaroff JG,
Klijn CJM,
Malik R,
Dichgans M,
Sargurupremraj M,
Tatlisumak T,
Amouyel P,
Debette S,
Rinkel GJE,
Worrall BB,
Pera J,
Slowik A,
Gaál-Paavola EI,
Niemelä M,
Jääskeläinen JE,
von Und Zu Fraunberg M,
Lindgren A,
Broderick JP,
Werring DJ,
Woo D,
Redon R,
Bijlenga P,
Kamatani Y,
Veldink JH,
Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Mingardo E,
Beaman G,
Grote P,
Nordenskjöld A,
Newman W,
Woolf AS,
Eckstein M,
Hilger AC,
Dworschak GC,
Rösch W,
Ebert AK,
Stein R
and 54 more — show all
Brusco A,
Di Grazia M,
Tamer A,
Torres FM,
Hernandez JL,
Erben P,
Maj C,
Olmos JM,
Riancho JA,
Valero C,
Hostettler IC,
Houlden H,
Werring DJ,
Schumacher J,
Gehlen J,
Giel AS,
Buerfent BC,
Arkani S,
Åkesson E,
Rotstein E,
Ludwig M,
Holmdahl G,
Giorgio E,
Berettini A,
Keene D,
Cervellione RM,
Younsi N,
Ortlieb M,
Oswald J,
Haid B,
Promm M,
Neissner C,
Hirsch K,
Stehr M,
Schäfer FM,
Schmiedeke E,
Boemers TM,
van Rooij IALM,
Feitz WFJ,
Marcelis CLM,
Lacher M,
Nelson J,
Ure B,
Fortmann C,
Gale DP,
Chan MMY,
Ludwig KU,
Nöthen MM,
Heilmann S,
Zwink N,
Jenetzky E,
Odermatt B,
Knapp M,
Reutter H
Communications biology · 2022 · PMID 36352089 · open access
4 pages
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Simón-Sánchez J,
Schulte C,
Bras JM,
Sharma M,
Gibbs JR,
Berg D,
Paisan-Ruiz C,
Lichtner P,
Scholz SW,
Hernandez DG,
Krüger R,
Federoff M
and 35 more — show all
Klein C,
Goate A,
Perlmutter J,
Bonin M,
Nalls MA,
Illig T,
Gieger C,
Houlden H,
Steffens M,
Okun MS,
Racette BA,
Cookson MR,
Foote KD,
Fernandez HH,
Traynor BJ,
Schreiber S,
Arepalli S,
Zonozi R,
Gwinn K,
van der Brug M,
Lopez G,
Chanock SJ,
Schatzkin A,
Park Y,
Hollenbeck A,
Gao J,
Huang X,
Wood NW,
Lorenz D,
Deuschl G,
Chen H,
Riess O,
Hardy JA,
Singleton AB,
Gasser T
Nature genetics · 2009 · PMID 19915575 · open access
1 page
Genome-Wide Association Study Identifies Risk Loci for Cluster Headache
O'Connor E,
Fourier C,
Ran C,
Sivakumar P,
Liesecke F,
Southgate L,
Harder AVE,
Vijfhuizen LS,
Yip J,
Giffin N,
Silver N,
Ahmed F
and 28 more — show all
Hostettler IC,
Davies B,
Cader MZ,
Simpson BS,
Sullivan R,
Efthymiou S,
Adebimpe J,
Quinn O,
Campbell C,
Cavalleri GL,
Vikelis M,
Kelderman T,
Paemeleire K,
Kilbride E,
Grangeon L,
Lagrata S,
Danno D,
Trembath R,
Wood NW,
Kockum I,
Winsvold BS,
Steinberg A,
Sjöstrand C,
Waldenlind E,
Vandrovcova J,
Houlden H,
Matharu M,
Belin AC
Annals of neurology · 2021 · PMID 34184781 · 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.