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8 matches for
Rahmioglu N.
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Gallagher CS,
Mäkinen N,
Harris HR,
Rahmioglu N,
Uimari O,
Cook JP,
Shigesi N,
Ferreira T,
Velez-Edwards DR,
Edwards TL,
Mortlock S,
Ruhioglu Z
and 24 more — show all
Day F,
Becker CM,
Karhunen V,
Martikainen H,
Järvelin MR,
Cantor RM,
Ridker PM,
Terry KL,
Buring JE,
Gordon SD,
Medland SE,
Montgomery GW,
Nyholt DR,
Hinds DA,
Tung JY,
Perry JRB,
Lind PA,
Painter JN,
Martin NG,
Morris AP,
Chasman DI,
Missmer SA,
Zondervan KT,
Morton CC
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
12 pages+
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Chambers JC,
Zhang W,
Sehmi J,
Li X,
Wass MN,
Van der Harst P,
Holm H,
Sanna S,
Kavousi M,
Baumeister SE,
Coin LJ,
Deng G
and 124 more — show all
Gieger C,
Heard-Costa NL,
Hottenga JJ,
Kühnel B,
Kumar V,
Lagou V,
Liang L,
Luan J,
Vidal PM,
Mateo Leach I,
O'Reilly PF,
Peden JF,
Rahmioglu N,
Soininen P,
Speliotes EK,
Yuan X,
Thorleifsson G,
Alizadeh BZ,
Atwood LD,
Borecki IB,
Brown MJ,
Charoen P,
Cucca F,
Das D,
de Geus EJ,
Dixon AL,
Döring A,
Ehret G,
Eyjolfsson GI,
Farrall M,
Forouhi NG,
Friedrich N,
Goessling W,
Gudbjartsson DF,
Harris TB,
Hartikainen AL,
Heath S,
Hirschfield GM,
Hofman A,
Homuth G,
Hyppönen E,
Janssen HL,
Johnson T,
Kangas AJ,
Kema IP,
Kühn JP,
Lai S,
Lathrop M,
Lerch MM,
Li Y,
Liang TJ,
Lin JP,
Loos RJ,
Martin NG,
Moffatt MF,
Montgomery GW,
Munroe PB,
Musunuru K,
Nakamura Y,
O'Donnell CJ,
Olafsson I,
Penninx BW,
Pouta A,
Prins BP,
Prokopenko I,
Puls R,
Ruokonen A,
Savolainen MJ,
Schlessinger D,
Schouten JN,
Seedorf U,
Sen-Chowdhry S,
Siminovitch KA,
Smit JH,
Spector TD,
Tan W,
Teslovich TM,
Tukiainen T,
Uitterlinden AG,
Van der Klauw MM,
Vasan RS,
Wallace C,
Wallaschofski H,
Wichmann HE,
Willemsen G,
Würtz P,
Xu C,
Yerges-Armstrong LM,
Abecasis GR,
Ahmadi KR,
Boomsma DI,
Caulfield M,
Cookson WO,
van Duijn CM,
Froguel P,
Matsuda K,
McCarthy MI,
Meisinger C,
Mooser V,
Pietiläinen KH,
Schumann G,
Snieder H,
Sternberg MJ,
Stolk RP,
Thomas HC,
Thorsteinsdottir U,
Uda M,
Waeber G,
Wareham NJ,
Waterworth DM,
Watkins H,
Whitfield JB,
Witteman JC,
Wolffenbuttel BH,
Fox CS,
Ala-Korpela M,
Stefansson K,
Vollenweider P,
Völzke H,
Schadt EE,
Scott J,
Järvelin MR,
Elliott P,
Kooner JS
Alcohol Genome-wide Association (AlcGen) Consortium · Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study and 5 more consortia
Nature genetics · 2011 · PMID 22001757
9 pages
The phenotypic and genetic association between endometriosis and immunological diseases
Shigesi N,
Harris HR,
Fang H,
Ndungu A,
Lincoln MR,
Cotsapas C,
Knight J,
Missmer SA,
Morris AP,
Becker CM,
Rahmioglu N,
Zondervan KT
International Endometriosis Genome Consortium · 23andMe Research Team
Human reproduction (Oxford, England) · 2025 · PMID 40262193 · open access
9 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
Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism
Sapkota Y,
Steinthorsdottir V,
Morris AP,
Fassbender A,
Rahmioglu N,
De Vivo I,
Buring JE,
Zhang F,
Edwards TL,
Jones S,
O D,
Peterse D
and 30 more — show all
Rexrode KM,
Ridker PM,
Schork AJ,
MacGregor S,
Martin NG,
Becker CM,
Adachi S,
Yoshihara K,
Enomoto T,
Takahashi A,
Kamatani Y,
Matsuda K,
Kubo M,
Thorleifsson G,
Geirsson RT,
Thorsteinsdottir U,
Wallace LM,
Yang J,
Velez Edwards DR,
Nyegaard M,
Nyegaard M,
Low SK,
Zondervan KT,
Missmer SA,
D'Hooghe T,
Montgomery GW,
Chasman DI,
Stefansson K,
Tung JY,
Nyholt DR
iPSYCH-SSI-Broad Group
Nature communications · 2017 · PMID 28537267 · open access
1 page
Large-scale meta-analysis highlights the hypothalamic-pituitary-gonadal axis in the genetic regulation of menstrual cycle length
Laisk T,
Kukuškina V,
Palmer D,
Laber S,
Chen CY,
Ferreira T,
Rahmioglu N,
Zondervan K,
Becker C,
Smoller JW,
Lippincott M,
Salumets A
and 5 more — show all
Human molecular genetics · 2018 · PMID 30202859 · 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.