For researchers
Is your paper here?
2,676 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.
87 matches for
Ni C,
showing the first 7.
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy
Li M,
Wang L,
Shi DC,
Foo JN,
Zhong Z,
Khor CC,
Lanzani C,
Citterio L,
Salvi E,
Yin PR,
Bei JX,
Wang L
and 13 more — show all
Liao YH,
Chen J,
Chen QK,
Xu G,
Jiang GR,
Wan JX,
Chen MH,
Chen N,
Zhang H,
Zeng YX,
Liu ZH,
Liu JJ,
Yu XQ
Journal of the American Society of Nephrology : JASN · 2020 · PMID 32912934
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
Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease
Ortiz Fernández L,
Coit P,
Yilmaz V,
Yentür SP,
Alibaz-Oner F,
Aksu K,
Erken E,
Düzgün N,
Keser G,
Cefle A,
Yazici A,
Ergen A
and 25 more — show all
Alpsoy E,
Salvarani C,
Casali B,
Kısacık B,
Kötter I,
Henes J,
Çınar M,
Schaefer A,
Nohutcu RM,
Zhernakova A,
Wijmenga C,
Takeuchi F,
Harihara S,
Kaburaki T,
Messedi M,
Song YW,
Kaşifoğlu T,
Carmona FD,
Guthridge JM,
James JA,
Martin J,
González Escribano MF,
Saruhan-Direskeneli G,
Direskeneli H,
Sawalha AH
Arthritis & rheumatology (Hoboken, N.J.) · 2021 · PMID 33393726
1 page
TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study
Meijer AJM,
Diepstraten FA,
Langer T,
Broer L,
Domingo IK,
Clemens E,
Uitterlinden AG,
de Vries ACH,
van Grotel M,
Vermeij WP,
Ozinga RA,
Binder H
and 43 more — show all
Byrne J,
van Dulmen-den Broeder E,
Garrè ML,
Grabow D,
Kaatsch P,
Kaiser M,
Kenborg L,
Winther JF,
Rechnitzer C,
Hasle H,
Kepak T,
Kepakova K,
Tissing WJE,
van der Kooi ALF,
Kremer LCM,
Kruseova J,
Pluijm SMF,
Kuehni CE,
van der Pal HJH,
Parfitt R,
Spix C,
Tillmanns A,
Deuster D,
Matulat P,
Calaminus G,
Hoetink AE,
Elsner S,
Gebauer J,
Haupt R,
Lackner H,
Blattmann C,
Neggers SJCMM,
Rassekh SR,
Wright GEB,
Brooks B,
Nagtegaal AP,
Drögemöller BI,
Ross CJD,
Bhavsar AP,
Am Zehnhoff-Dinnesen AG,
Carleton BC,
Zolk O,
van den Heuvel-Eibrink MM
PanCareLIFE Consortium · and the CPNDS Consortium
NPJ precision oncology · 2021 · PMID 34262104 · open access
1 page
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis
Schack LMH,
Naderi E,
Fachal L,
Dorling L,
Luccarini C,
Dunning AM,
Ong EHW,
Chua MLK,
Langendijk JA,
Alizadeh BZ,
Overgaard J,
Eriksen JG
and 2 more — show all
Head and Neck Group of the Radiogenomics Consortium · Danish Head and Neck Cancer Group (DAHANCA)
British journal of cancer · 2022 · PMID 35039627 · open access
1 page
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
and 128 more — show all
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
1 page
Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study
Borrego-Yaniz G,
Ortiz-Fernández L,
Madrid-Paredes A,
Kerick M,
Hernández-Rodríguez J,
Mackie SL,
Vaglio A,
Castañeda S,
Solans R,
Mestre-Torres J,
Khalidi N,
Langford CA
and 39 more — show all
Ytterberg S,
Beretta L,
Govoni M,
Emmi G,
Cimmino MA,
Witte T,
Neumann T,
Holle J,
Schönau V,
Pugnet G,
Papo T,
Haroche J,
Mahr A,
Mouthon L,
Molberg Ø,
Diamantopoulos AP,
Voskuyl A,
Daikeler T,
Berger CT,
Molloy ES,
Blockmans D,
van Sleen Y,
Iles M,
Sorensen L,
Luqmani R,
Reynolds G,
Bukhari M,
Bhagat S,
Ortego-Centeno N,
Brouwer E,
Lamprecht P,
Klapa S,
Salvarani C,
Merkel PA,
Cid MC,
González-Gay MA,
Morgan AW,
Martin J,
Márquez A
Spanish GCA Group · UK GCA Consortium and 1 more consortia
The Lancet. Rheumatology · 2024 · PMID 38734017 · 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.