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2,665 papers hold this site up. Every variant and condition page names
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29 matches for
Li A,
showing the first 9.
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
van Rheenen W,
van der Spek RAA,
Bakker MK,
van Vugt JJFA,
Hop PJ,
Zwamborn RAJ,
de Klein N,
Westra HJ,
Bakker OB,
Deelen P,
Shireby G,
Hannon E
and 180 more — show all
Moisse M,
Baird D,
Restuadi R,
Dolzhenko E,
Dekker AM,
Gawor K,
Westeneng HJ,
Tazelaar GHP,
van Eijk KR,
Kooyman M,
Byrne RP,
Doherty M,
Heverin M,
Al Khleifat A,
Iacoangeli A,
Shatunov A,
Ticozzi N,
Cooper-Knock J,
Smith BN,
Gromicho M,
Chandran S,
Pal S,
Morrison KE,
Shaw PJ,
Hardy J,
Orrell RW,
Sendtner M,
Meyer T,
Başak N,
van der Kooi AJ,
Ratti A,
Fogh I,
Gellera C,
Lauria G,
Corti S,
Cereda C,
Sproviero D,
D'Alfonso S,
Sorarù G,
Siciliano G,
Filosto M,
Padovani A,
Chiò A,
Calvo A,
Moglia C,
Brunetti M,
Canosa A,
Grassano M,
Beghi E,
Pupillo E,
Logroscino G,
Nefussy B,
Osmanovic A,
Nordin A,
Lerner Y,
Zabari M,
Gotkine M,
Baloh RH,
Bell S,
Vourc'h P,
Corcia P,
Couratier P,
Millecamps S,
Meininger V,
Salachas F,
Mora Pardina JS,
Assialioui A,
Rojas-García R,
Dion PA,
Ross JP,
Ludolph AC,
Weishaupt JH,
Brenner D,
Freischmidt A,
Bensimon G,
Brice A,
Durr A,
Payan CAM,
Saker-Delye S,
Wood NW,
Topp S,
Rademakers R,
Tittmann L,
Lieb W,
Franke A,
Ripke S,
Braun A,
Kraft J,
Whiteman DC,
Olsen CM,
Uitterlinden AG,
Hofman A,
Rietschel M,
Cichon S,
Nöthen MM,
Amouyel P,
Traynor BJ,
Singleton AB,
Mitne Neto M,
Cauchi RJ,
Ophoff RA,
Wiedau-Pazos M,
Lomen-Hoerth C,
van Deerlin VM,
Grosskreutz J,
Roediger A,
Gaur N,
Jörk A,
Barthel T,
Theele E,
Ilse B,
Stubendorff B,
Witte OW,
Steinbach R,
Hübner CA,
Graff C,
Brylev L,
Fominykh V,
Demeshonok V,
Ataulina A,
Rogelj B,
Koritnik B,
Zidar J,
Ravnik-Glavač M,
Glavač D,
Stević Z,
Drory V,
Povedano M,
Blair IP,
Kiernan MC,
Benyamin B,
Henderson RD,
Furlong S,
Mathers S,
McCombe PA,
Needham M,
Ngo ST,
Nicholson GA,
Pamphlett R,
Rowe DB,
Steyn FJ,
Williams KL,
Mather KA,
Sachdev PS,
Henders AK,
Wallace L,
de Carvalho M,
Pinto S,
Petri S,
Weber M,
Rouleau GA,
Silani V,
Curtis CJ,
Breen G,
Glass JD,
Brown RH Jr,
Landers JE,
Shaw CE,
Andersen PM,
Groen EJN,
van Es MA,
Pasterkamp RJ,
Fan D,
Garton FC,
McRae AF,
Davey Smith G,
Gaunt TR,
Eberle MA,
Mill J,
McLaughlin RL,
Hardiman O,
Kenna KP,
Wray NR,
Tsai E,
Runz H,
Franke L,
Al-Chalabi A,
Van Damme P,
van den Berg LH,
Veldink JH
SLALOM Consortium · PARALS Consortium and 2 more consortia
Nature genetics · 2021 · PMID 34873335 · open access
3 pages
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
Liu X,
Invernizzi P,
Lu Y,
Kosoy R,
Lu Y,
Bianchi I,
Podda M,
Xu C,
Xie G,
Macciardi F,
Selmi C,
Lupoli S
and 61 more — show all
Shigeta R,
Ransom M,
Lleo A,
Lee AT,
Mason AL,
Myers RP,
Peltekian KM,
Ghent CN,
Bernuzzi F,
Zuin M,
Rosina F,
Borghesio E,
Floreani A,
Lazzari R,
Niro G,
Andriulli A,
Muratori L,
Muratori P,
Almasio PL,
Andreone P,
Margotti M,
Brunetto M,
Coco B,
Alvaro D,
Bragazzi MC,
Marra F,
Pisano A,
Rigamonti C,
Colombo M,
Marzioni M,
Benedetti A,
Fabris L,
Strazzabosco M,
Portincasa P,
Palmieri VO,
Tiribelli C,
Croce L,
Bruno S,
Rossi S,
Vinci M,
Prisco C,
Mattalia A,
Toniutto P,
Picciotto A,
Galli A,
Ferrari C,
Ferrari C,
Colombo S,
Casella G,
Morini L,
Caporaso N,
Colli A,
Spinzi G,
Montanari R,
Gregersen PK,
Heathcote EJ,
Hirschfield GM,
Siminovitch KA,
Amos CI,
Gershwin ME,
Seldin MF
Nature genetics · 2010 · PMID 20639880
2 pages
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13
Leslie EJ,
Carlson JC,
Shaffer JR,
Feingold E,
Wehby G,
Laurie CA,
Jain D,
Laurie CC,
Doheny KF,
McHenry T,
Resick J,
Sanchez C
and 43 more — show all
Jacobs J,
Emanuele B,
Vieira AR,
Neiswanger K,
Lidral AC,
Valencia-Ramirez LC,
Lopez-Palacio AM,
Valencia DR,
Arcos-Burgos M,
Czeizel AE,
Field LL,
Padilla CD,
Cutiongco-de la Paz EM,
Deleyiannis F,
Christensen K,
Munger RG,
Lie RT,
Wilcox A,
Romitti PA,
Castilla EE,
Mereb JC,
Poletta FA,
Orioli IM,
Carvalho FM,
Hecht JT,
Blanton SH,
Buxó CJ,
Butali A,
Mossey PA,
Adeyemo WL,
James O,
Braimah RO,
Aregbesola BS,
Eshete MA,
Abate F,
Koruyucu M,
Seymen F,
Ma L,
de Salamanca JE,
Weinberg SM,
Moreno L,
Murray JC,
Marazita ML
Human molecular genetics · 2016 · PMID 27033726
2 pages
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants
Wood AR,
Jonsson A,
Jackson AU,
Wang N,
van Leewen N,
Palmer ND,
Kobes S,
Deelen J,
Boquete-Vilarino L,
Paananen J,
Stančáková A,
Boomsma DI
and 40 more — show all
de Geus EJC,
Eekhoff EMW,
Fritsche A,
Kramer M,
Nijpels G,
Simonis-Bik A,
van Haeften TW,
Mahajan A,
Boehnke M,
Bergman RN,
Tuomilehto J,
Collins FS,
Mohlke KL,
Banasik K,
Groves CJ,
McCarthy MI,
Pearson ER,
Natali A,
Mari A,
Buchanan TA,
Taylor KD,
Xiang AH,
Xiang AH,
Gjesing AP,
Grarup N,
Eiberg H,
Pedersen O,
Chen YD,
Laakso M,
Norris JM,
Smith U,
Wagenknecht LE,
Baier L,
Bowden DW,
Hansen T,
Walker M,
Watanabe RM,
't Hart LM,
Hanson RL,
Frayling TM
Diabetes Research on Patient Stratification (DIRECT)
Diabetes · 2017 · PMID 28490609 · open access
2 pages
Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood
Adkins DE,
Clark SL,
Copeland WE,
Kennedy M,
Conway K,
Angold A,
Maes H,
Liu Y,
Kumar G,
Erkanli A,
Patkar AA,
Silberg J
and 7 more — show all
Twin research and human genetics : the official journal of the International Society for Twin Studies · 2015 · PMID 26081443
1 page
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3
Leslie EJ,
Liu H,
Carlson JC,
Shaffer JR,
Feingold E,
Wehby G,
Laurie CA,
Jain D,
Laurie CC,
Doheny KF,
McHenry T,
Resick J
and 46 more — show all
Sanchez C,
Jacobs J,
Emanuele B,
Vieira AR,
Neiswanger K,
Standley J,
Czeizel AE,
Deleyiannis F,
Christensen K,
Munger RG,
Lie RT,
Wilcox A,
Romitti PA,
Field LL,
Padilla CD,
Cutiongco-de la Paz EM,
Lidral AC,
Valencia-Ramirez LC,
Lopez-Palacio AM,
Valencia DR,
Arcos-Burgos M,
Castilla EE,
Mereb JC,
Poletta FA,
Orioli IM,
Carvalho FM,
Hecht JT,
Blanton SH,
Buxó CJ,
Butali A,
Mossey PA,
Adeyemo WL,
James O,
Braimah RO,
Aregbesola BS,
Eshete MA,
Deribew M,
Koruyucu M,
Seymen F,
Ma L,
de Salamanca JE,
Weinberg SM,
Moreno L,
Cornell RA,
Murray JC,
Marazita ML
American journal of human genetics · 2016 · PMID 27018472
1 page
Genetic Factors Associated with Prostate Cancer Conversion from Active Surveillance to Treatment
Jiang Y,
Meyers TJ,
Emeka AA,
Cooley LF,
Cooper PR,
Lancki N,
Helenowski I,
Kachuri L,
Lin DW,
Stanford JL,
Newcomb LF,
Kolb S
and 85 more — show all
Finelli A,
Fleshner NE,
Komisarenko M,
Eastham JA,
Ehdaie B,
Benfante N,
Logothetis CJ,
Gregg JR,
Perez CA,
Garza S,
Kim J,
Marks LS,
Delfin M,
Barsa D,
Vesprini D,
Klotz LH,
Loblaw A,
Mamedov A,
Goldenberg SL,
Higano CS,
Spillane M,
Wu E,
Carter HB,
Pavlovich CP,
Mamawala M,
Landis T,
Carroll PR,
Chan JM,
Cooperberg MR,
Cowan JE,
Morgan TM,
Siddiqui J,
Martin R,
Klein EA,
Brittain K,
Gotwald P,
Barocas DA,
Dallmer JR,
Gordetsky JB,
Steele P,
Kundu SD,
Stockdale J,
Roobol MJ,
Venderbos LDF,
Sanda MG,
Arnold R,
Patil D,
Evans CP,
Dall'Era MA,
Vij A,
Costello AJ,
Chow K,
Corcoran NM,
Rais-Bahrami S,
Phares C,
Scherr DS,
Flynn T,
Karnes RJ,
Koch M,
Dhondt CR,
Nelson JB,
McBride D,
Cookson MS,
Stratton KL,
Farriester S,
Hemken E,
Stadler WM,
Pera T,
Banionyte D,
Bianco FJ Jr,
Lopez IH,
Loeb S,
Taneja SS,
Byrne N,
Amling CL,
Martinez A,
Boileau L,
Gaylis FD,
Petkewicz J,
Kirwen N,
Helfand BT,
Xu J,
Scholtens DM,
Catalona WJ,
Witte JS
HGG advances · 2022 · PMID 34993496 · open access
1 page
Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study
Chia R,
Saez-Atienzar S,
Murphy N,
Chiò A,
Blauwendraat C,
Roda RH,
Tienari PJ,
Kaminski HJ,
Ricciardi R,
Guida M,
De Rosa A,
Petrucci L
and 4 more — show all
International Myasthenia Gravis Genomics Consortium
Proceedings of the National Academy of Sciences of the United States of America · 2022 · PMID 35074870 · open access
1 page
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes
Mukhopadhyay N,
Feingold E,
Moreno-Uribe L,
Wehby G,
Valencia-Ramirez LC,
Restrepo Muñeton CP,
Padilla C,
Deleyiannis F,
Christensen K,
Poletta FA,
Orioli IM,
Hecht JT
and 9 more — show all
Genetic epidemiology · 2022 · PMID 35191549
1 page
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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.