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3 matches for
Ulrich A.
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
Lagou V,
Jiang L,
Ulrich A,
Zudina L,
González KSG,
Balkhiyarova Z,
Faggian A,
Maina JG,
Chen S,
Todorov PV,
Sharapov S,
David A
and 84 more — show all
Marullo L,
Mägi R,
Rujan RM,
Ahlqvist E,
Thorleifsson G,
Gao Η,
Εvangelou Ε,
Benyamin B,
Scott RA,
Isaacs A,
Zhao JH,
Willems SM,
Johnson T,
Gieger C,
Grallert H,
Meisinger C,
Müller-Nurasyid M,
Strawbridge RJ,
Goel A,
Rybin D,
Albrecht E,
Jackson AU,
Stringham HM,
Corrêa IR Jr,
Farber-Eger E,
Steinthorsdottir V,
Uitterlinden AG,
Munroe PB,
Brown MJ,
Schmidberger J,
Holmen O,
Thorand B,
Hveem K,
Wilsgaard T,
Mohlke KL,
Wang Z,
Shmeliov A,
den Hoed M,
Loos RJF,
Kratzer W,
Haenle M,
Koenig W,
Boehm BO,
Tan TM,
Tomas A,
Salem V,
Barroso I,
Tuomilehto J,
Boehnke M,
Florez JC,
Hamsten A,
Watkins H,
Njølstad I,
Wichmann HE,
Caulfield MJ,
Khaw KT,
van Duijn CM,
Hofman A,
Wareham NJ,
Langenberg C,
Whitfield JB,
Martin NG,
Montgomery G,
Scapoli C,
Tzoulaki I,
Elliott P,
Thorsteinsdottir U,
Stefansson K,
Brittain EL,
McCarthy MI,
Froguel P,
Sexton PM,
Wootten D,
Groop L,
Dupuis J,
Meigs JB,
Deganutti G,
Demirkan A,
Pers TH,
Reynolds CA,
Aulchenko YS,
Kaakinen MA,
Jones B,
Prokopenko I
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
Rhodes CJ,
Batai K,
Bleda M,
Haimel M,
Southgate L,
Germain M,
Pauciulo MW,
Hadinnapola C,
Aman J,
Girerd B,
Arora A,
Knight J
and 106 more — show all
Hanscombe KB,
Karnes JH,
Kaakinen M,
Gall H,
Ulrich A,
Harbaum L,
Cebola I,
Ferrer J,
Lutz K,
Swietlik EM,
Ahmad F,
Amouyel P,
Archer SL,
Argula R,
Austin ED,
Badesch D,
Bakshi S,
Barnett C,
Benza R,
Bhatt N,
Bogaard HJ,
Burger CD,
Chakinala M,
Church C,
Coghlan JG,
Condliffe R,
Corris PA,
Danesino C,
Debette S,
Elliott CG,
Elwing J,
Eyries M,
Fortin T,
Franke A,
Frantz RP,
Frost A,
Garcia JGN,
Ghio S,
Ghofrani HA,
Gibbs JSR,
Harley J,
He H,
Hill NS,
Hirsch R,
Houweling AC,
Howard LS,
Ivy D,
Kiely DG,
Klinger J,
Kovacs G,
Lahm T,
Laudes M,
Machado RD,
MacKenzie Ross RV,
Marsolo K,
Martin LJ,
Moledina S,
Montani D,
Nathan SD,
Newnham M,
Olschewski A,
Olschewski H,
Oudiz RJ,
Ouwehand WH,
Peacock AJ,
Pepke-Zaba J,
Rehman Z,
Robbins I,
Roden DM,
Rosenzweig EB,
Saydain G,
Scelsi L,
Schilz R,
Seeger W,
Shaffer CM,
Simms RW,
Simon M,
Sitbon O,
Suntharalingam J,
Tang H,
Tchourbanov AY,
Thenappan T,
Torres F,
Toshner MR,
Treacy CM,
Vonk Noordegraaf A,
Waisfisz Q,
Walsworth AK,
Walter RE,
Wharton J,
White RJ,
Wilt J,
Wort SJ,
Yung D,
Lawrie A,
Humbert M,
Soubrier F,
Trégouët DA,
Prokopenko I,
Kittles R,
Gräf S,
Nichols WC,
Trembath RC,
Desai AA,
Morrell NW,
Wilkins MR
UK NIHR BioResource Rare Diseases Consortium · UK PAH Cohort Study Consortium and 1 more consortia
The Lancet. Respiratory medicine · 2019 · PMID 30527956 · open access
4 pages
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou V,
Mägi R,
Hottenga JJ,
Grallert H,
Perry JRB,
Bouatia-Naji N,
Marullo L,
Rybin D,
Jansen R,
Min JL,
Dimas AS,
Ulrich A
and 192 more — show all
Zudina L,
Gådin JR,
Jiang L,
Faggian A,
Bonnefond A,
Fadista J,
Stathopoulou MG,
Isaacs A,
Willems SM,
Navarro P,
Tanaka T,
Jackson AU,
Montasser ME,
O'Connell JR,
Bielak LF,
Webster RJ,
Saxena R,
Stafford JM,
Pourcain BS,
Timpson NJ,
Salo P,
Shin SY,
Amin N,
Smith AV,
Li G,
Verweij N,
Goel A,
Ford I,
Johnson PCD,
Johnson T,
Kapur K,
Thorleifsson G,
Strawbridge RJ,
Rasmussen-Torvik LJ,
Esko T,
Mihailov E,
Fall T,
Fraser RM,
Mahajan A,
Kanoni S,
Giedraitis V,
Kleber ME,
Silbernagel G,
Meyer J,
Müller-Nurasyid M,
Ganna A,
Sarin AP,
Yengo L,
Shungin D,
Luan J,
Horikoshi M,
An P,
Sanna S,
Boettcher Y,
Rayner NW,
Nolte IM,
Zemunik T,
Iperen EV,
Kovacs P,
Hastie ND,
Wild SH,
McLachlan S,
Campbell S,
Polasek O,
Carlson O,
Egan J,
Kiess W,
Willemsen G,
Kuusisto J,
Laakso M,
Dimitriou M,
Hicks AA,
Rauramaa R,
Bandinelli S,
Thorand B,
Liu Y,
Miljkovic I,
Lind L,
Doney A,
Perola M,
Hingorani A,
Kivimaki M,
Kumari M,
Bennett AJ,
Groves CJ,
Herder C,
Koistinen HA,
Kinnunen L,
Faire U,
Bakker SJL,
Uusitupa M,
Palmer CNA,
Jukema JW,
Sattar N,
Pouta A,
Snieder H,
Boerwinkle E,
Pankow JS,
Magnusson PK,
Krus U,
Scapoli C,
de Geus EJCN,
Blüher M,
Wolffenbuttel BHR,
Province MA,
Abecasis GR,
Meigs JB,
Hovingh GK,
Lindström J,
Wilson JF,
Wright AF,
Dedoussis GV,
Bornstein SR,
Schwarz PEH,
Tönjes A,
Winkelmann BR,
Boehm BO,
März W,
Metspalu A,
Price JF,
Deloukas P,
Körner A,
Lakka TA,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Bergman RN,
Tuomilehto J,
Wareham NJ,
Langenberg C,
Männistö S,
Franks PW,
Hayward C,
Vitart V,
Kaprio J,
Visvikis-Siest S,
Balkau B,
Altshuler D,
Rudan I,
Stumvoll M,
Campbell H,
van Duijn CM,
Gieger C,
Illig T,
Ferrucci L,
Pedersen NL,
Pramstaller PP,
Boehnke M,
Frayling TM,
Shuldiner AR,
Peyser PA,
Kardia SLR,
Palmer LJ,
Penninx BW,
Meneton P,
Harris TB,
Navis G,
Harst PV,
Smith GD,
Forouhi NG,
Loos RJF,
Salomaa V,
Soranzo N,
Boomsma DI,
Groop L,
Tuomi T,
Hofman A,
Munroe PB,
Gudnason V,
Siscovick DS,
Watkins H,
Lecoeur C,
Vollenweider P,
Franco-Cereceda A,
Eriksson P,
Jarvelin MR,
Stefansson K,
Hamsten A,
Nicholson G,
Karpe F,
Dermitzakis ET,
Lindgren CM,
McCarthy MI,
Froguel P,
Kaakinen MA,
Lyssenko V,
Watanabe RM,
Ingelsson E,
Florez JC,
Dupuis J,
Barroso I,
Morris AP,
Prokopenko I
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
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.