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2,662 papers hold this site up. Every variant and condition page names
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13 matches for
Ates A.
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
Law PJ,
Timofeeva M,
Fernandez-Rozadilla C,
Broderick P,
Studd J,
Fernandez-Tajes J,
Farrington S,
Svinti V,
Palles C,
Orlando G,
Sud A,
Holroyd A
and 86 more — show all
Penegar S,
Theodoratou E,
Vaughan-Shaw P,
Campbell H,
Zgaga L,
Hayward C,
Campbell A,
Harris S,
Deary IJ,
Starr J,
Gatcombe L,
Pinna M,
Briggs S,
Martin L,
Jaeger E,
Sharma-Oates A,
East J,
Leedham S,
Arnold R,
Johnstone E,
Wang H,
Kerr D,
Kerr R,
Maughan T,
Kaplan R,
Al-Tassan N,
Palin K,
Hänninen UA,
Cajuso T,
Tanskanen T,
Kondelin J,
Kaasinen E,
Sarin AP,
Eriksson JG,
Rissanen H,
Knekt P,
Pukkala E,
Jousilahti P,
Salomaa V,
Ripatti S,
Palotie A,
Renkonen-Sinisalo L,
Lepistö A,
Böhm J,
Mecklin JP,
Buchanan DD,
Win AK,
Hopper J,
Jenkins ME,
Lindor NM,
Newcomb PA,
Gallinger S,
Duggan D,
Casey G,
Hoffmann P,
Nöthen MM,
Jöckel KH,
Easton DF,
Pharoah PDP,
Peto J,
Canzian F,
Swerdlow A,
Eeles RA,
Kote-Jarai Z,
Muir K,
Pashayan N,
Harkin A,
Allan K,
McQueen J,
Paul J,
Iveson T,
Saunders M,
Butterbach K,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Kirac I,
Matošević P,
Hofer P,
Brezina S,
Gsur A,
Cheadle JP,
Aaltonen LA,
Tomlinson I,
Houlston RS,
Dunlop MG
PRACTICAL consortium
Nature communications · 2019 · PMID 31089142 · open access
12 pages+
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Ferreira MA,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
van Dongen J,
Lu Y,
Rüschendorf F
and 54 more — show all
Esparza-Gordillo J,
Medway CW,
Mountjoy E,
Burrows K,
Hummel O,
Grosche S,
Brumpton BM,
Witte JS,
Hottenga JJ,
Willemsen G,
Zheng J,
Rodríguez E,
Hotze M,
Franke A,
Revez JA,
Beesley J,
Matheson MC,
Dharmage SC,
Bain LM,
Fritsche LG,
Gabrielsen ME,
Balliu B,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Arnold A,
Homuth G,
Schmidt CO,
Thompson PJ,
Martin NG,
Duffy DL,
Novak N,
Schulz H,
Karrasch S,
Gieger C,
Strauch K,
Melles RB,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PKE,
Jansen R,
Jorgenson E,
Lee YA,
Boomsma DI,
Almqvist C,
Karlsson R,
Koppelman GH,
Paternoster L
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study
Ortiz-Fernández L,
Saruhan-Direskeneli G,
Alibaz-Oner F,
Kaymaz-Tahra S,
Coit P,
Kong X,
Kiprianos AP,
Maughan RT,
Aydin SZ,
Aksu K,
Keser G,
Kamali S
and 59 more — show all
Inanc M,
Springer J,
Akar S,
Onen F,
Akkoc N,
Khalidi NA,
Koening C,
Karadag O,
Kiraz S,
Forbess L,
Langford CA,
McAlear CA,
Ozbalkan Z,
Yavuz S,
Çetin GY,
Alpay-Kanitez N,
Chung S,
Ates A,
Karaaslan Y,
McKinnon-Maksimowicz K,
Monach PA,
Ozer HTE,
Seyahi E,
Fresko I,
Cefle A,
Seo P,
Warrington KJ,
Ozturk MA,
Ytterberg SR,
Cobankara V,
Onat AM,
Duzgun N,
Bıcakcıgil M,
Yentür SP,
Lally L,
Manfredi AA,
Baldissera E,
Erken E,
Yazici A,
Kısacık B,
Kaşifoğlu T,
Dalkilic E,
Cuthbertson D,
Pagnoux C,
Sreih A,
Reales G,
Wallace C,
Wren JD,
Cunninghame-Graham DS,
Vyse TJ,
Sun Y,
Chen H,
Grayson PC,
Tombetti E,
Jiang L,
Mason JC,
Merkel PA,
Direskeneli H,
Sawalha AH
American journal of human genetics · 2021 · PMID 33308445
6 pages
Identification of multiple genetic susceptibility loci in Takayasu arteritis
Saruhan-Direskeneli G,
Hughes T,
Aksu K,
Keser G,
Coit P,
Aydin SZ,
Alibaz-Oner F,
Kamalı S,
Inanc M,
Carette S,
Hoffman GS,
Akar S
and 32 more — show all
Onen F,
Akkoc N,
Khalidi NA,
Koening C,
Karadag O,
Kiraz S,
Langford CA,
McAlear CA,
Ozbalkan Z,
Ates A,
Karaaslan Y,
Maksimowicz-McKinnon K,
Monach PA,
Ozer HT,
Seyahi E,
Fresko I,
Cefle A,
Seo P,
Warrington KJ,
Ozturk MA,
Ytterberg SR,
Cobankara V,
Onat AM,
Guthridge JM,
James JA,
Tunc E,
Duzgun N,
Bıcakcıgil M,
Yentür SP,
Merkel PA,
Direskeneli H,
Sawalha AH
American journal of human genetics · 2013 · PMID 23830517
4 pages
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population
Salo PP,
Havulinna AS,
Tukiainen T,
Raitakari O,
Lehtimäki T,
Kähönen M,
Kettunen J,
Männikkö M,
Eriksson JG,
Jula A,
Blankenberg S,
Zeller T
and 3 more — show all
Circulation. Cardiovascular genetics · 2017 · PMID 29237677 · open access
4 pages
Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties
Lee S,
Bijsterbosch JD,
Almagro FA,
Elliott L,
McCarthy P,
Taschler B,
Sala-Llonch R,
Beckmann CF,
Duff EP,
Smith SM,
Douaud G
NeuroImage · 2023 · PMID 36462729 · open access
3 pages
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
and 233 more — show all
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
Rioux JD,
Xavier RJ,
Taylor KD,
Silverberg MS,
Goyette P,
Huett A,
Green T,
Kuballa P,
Barmada MM,
Datta LW,
Shugart YY,
Griffiths AM
and 13 more — show all
Targan SR,
Ippoliti AF,
Bernard EJ,
Mei L,
Nicolae DL,
Regueiro M,
Schumm LP,
Steinhart AH,
Rotter JI,
Duerr RH,
Cho JH,
Daly MJ,
Brant SR
Nature genetics · 2007 · PMID 17435756
1 page
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study
Renauer PA,
Saruhan-Direskeneli G,
Coit P,
Adler A,
Aksu K,
Keser G,
Alibaz-Oner F,
Aydin SZ,
Kamali S,
Inanc M,
Carette S,
Cuthbertson D
and 43 more — show all
Hoffman GS,
Akar S,
Onen F,
Akkoc N,
Khalidi NA,
Koening C,
Karadag O,
Kiraz S,
Langford CA,
Maksimowicz-McKinnon K,
McAlear CA,
Ozbalkan Z,
Ates A,
Karaaslan Y,
Duzgun N,
Monach PA,
Ozer HT,
Erken E,
Ozturk MA,
Yazici A,
Cefle A,
Onat AM,
Kisacik B,
Pagnoux C,
Kasifoglu T,
Seyahi E,
Fresko I,
Seo P,
Sreih AG,
Warrington KJ,
Ytterberg SR,
Cobankara V,
Cunninghame-Graham DS,
Vyse TJ,
Pamuk ON,
Tunc SE,
Dalkilic E,
Bicakcigil M,
Yentur SP,
Wren JD,
Merkel PA,
Direskeneli H,
Sawalha AH
Arthritis & rheumatology (Hoboken, N.J.) · 2015 · PMID 25604533
1 page
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations
Hayes MG,
Urbanek M,
Ehrmann DA,
Armstrong LL,
Lee JY,
Sisk R,
Karaderi T,
Barber TM,
McCarthy MI,
Franks S,
Lindgren CM,
Welt CK
and 11 more — show all
Diamanti-Kandarakis E,
Panidis D,
Goodarzi MO,
Azziz R,
Zhang Y,
James RG,
Olivier M,
Kissebah AH,
Stener-Victorin E,
Legro RS,
Dunaif A
Reproductive Medicine Network
Nature communications · 2015 · PMID 26284813 · open access
1 page
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages
Park JY,
Lee D,
Lee JJ,
Gim J,
Gunasekaran TI,
Choi KY,
Kang S,
Do AR,
Jo J,
Park J,
Park K,
Li D
and 21 more — show all
Lee S,
Kim H,
Dhanasingh I,
Ghosh S,
Keum S,
Choi JH,
Song GJ,
Sael L,
Rhee S,
Lovestone S,
Kim E,
Moon SH,
Kim BC,
Kim S,
Saykin AJ,
Nho K,
Lee SH,
Farrer LA,
Jun GR,
Won S,
Lee KH
Alzheimer’s Disease Neuroimaging Initiative
Translational psychiatry · 2021 · PMID 34785643 · 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.