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2,662 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.
9 matches for
Groop PH.
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
Salem RM,
Todd JN,
Sandholm N,
Cole JB,
Chen WM,
Andrews D,
Pezzolesi MG,
McKeigue PM,
Hiraki LT,
Qiu C,
Nair V,
Di Liao C
and 76 more — show all
Cao JJ,
Valo E,
Onengut-Gumuscu S,
Smiles AM,
McGurnaghan SJ,
Haukka JK,
Harjutsalo V,
Brennan EP,
van Zuydam N,
Ahlqvist E,
Doyle R,
Ahluwalia TS,
Lajer M,
Hughes MF,
Park J,
Skupien J,
Spiliopoulou A,
Liu A,
Menon R,
Boustany-Kari CM,
Kang HM,
Nelson RG,
Klein R,
Klein BE,
Lee KE,
Gao X,
Mauer M,
Maestroni S,
Caramori ML,
de Boer IH,
Miller RG,
Guo J,
Boright AP,
Tregouet D,
Gyorgy B,
Snell-Bergeon JK,
Maahs DM,
Bull SB,
Canty AJ,
Palmer CNA,
Stechemesser L,
Paulweber B,
Weitgasser R,
Sokolovska J,
Rovīte V,
Pīrāgs V,
Prakapiene E,
Radzeviciene L,
Verkauskiene R,
Panduru NM,
Groop LC,
McCarthy MI,
Gu HF,
Möllsten A,
Falhammar H,
Brismar K,
Martin F,
Rossing P,
Costacou T,
Zerbini G,
Marre M,
Hadjadj S,
McKnight AJ,
Forsblom C,
McKay G,
Godson C,
Maxwell AP,
Kretzler M,
Susztak K,
Colhoun HM,
Krolewski A,
Paterson AD,
Groop PH,
Rich SS,
Hirschhorn JN,
Florez JC
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2019 · PMID 31537649
5 pages
Genome-Wide Association Study of Peripheral Artery Disease
van Zuydam NR,
Stiby A,
Abdalla M,
Austin E,
Dahlström EH,
Dahlström EH,
McLachlan S,
Vlachopoulou E,
Ahlqvist E,
Di Liao C,
Sandholm N,
Forsblom C
and 21 more — show all
Mahajan A,
Robertson NR,
Rayner NW,
Lindholm E,
Sinisalo J,
Perola M,
Kallio M,
Weiss E,
Price J,
Paterson A,
Klein B,
Salomaa V,
Palmer CNA,
Groop PH,
Groop L,
McCarthy MI,
de Andrade M,
Morris AP,
Hopewell JC,
Colhoun HM,
Kullo IJ
GoLEAD Consortium, SUMMIT Consortium†
Circulation. Genomic and precision medicine · 2021 · PMID 34601942 · open access
3 pages
New susceptibility loci associated with kidney disease in type 1 diabetes
Sandholm N,
Salem RM,
McKnight AJ,
Brennan EP,
Forsblom C,
Isakova T,
McKay GJ,
Williams WW,
Sadlier DM,
Mäkinen VP,
Swan EJ,
Palmer C
and 80 more — show all
Boright AP,
Ahlqvist E,
Deshmukh HA,
Keller BJ,
Huang H,
Ahola AJ,
Fagerholm E,
Gordin D,
Harjutsalo V,
He B,
Heikkilä O,
Hietala K,
Kytö J,
Lahermo P,
Lehto M,
Lithovius R,
Osterholm AM,
Parkkonen M,
Pitkäniemi J,
Rosengård-Bärlund M,
Saraheimo M,
Sarti C,
Söderlund J,
Soro-Paavonen A,
Syreeni A,
Thorn LM,
Tikkanen H,
Tolonen N,
Tryggvason K,
Tuomilehto J,
Wadén J,
Gill GV,
Prior S,
Guiducci C,
Mirel DB,
Taylor A,
Hosseini SM,
Parving HH,
Rossing P,
Tarnow L,
Ladenvall C,
Alhenc-Gelas F,
Lefebvre P,
Rigalleau V,
Roussel R,
Tregouet DA,
Maestroni A,
Maestroni S,
Falhammar H,
Gu T,
Möllsten A,
Cimponeriu D,
Ioana M,
Mota M,
Mota E,
Serafinceanu C,
Stavarachi M,
Hanson RL,
Nelson RG,
Kretzler M,
Colhoun HM,
Panduru NM,
Gu HF,
Brismar K,
Zerbini G,
Hadjadj S,
Marre M,
Groop L,
Lajer M,
Bull SB,
Waggott D,
Paterson AD,
Savage DA,
Bain SC,
Martin F,
Hirschhorn JN,
Godson C,
Florez JC,
Groop PH,
Maxwell AP
DCCT/EDIC Research Group
PLoS genetics · 2012 · PMID 23028342 · open access
2 pages
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
Sandholm N,
Cole JB,
Nair V,
Sheng X,
Liu H,
Ahlqvist E,
van Zuydam N,
Dahlström EH,
Fermin D,
Smyth LJ,
Salem RM,
Forsblom C
and 19 more — show all
Valo E,
Harjutsalo V,
Brennan EP,
McKay GJ,
Andrews D,
Doyle R,
Looker HC,
Nelson RG,
Palmer C,
McKnight AJ,
Godson C,
Maxwell AP,
Groop L,
McCarthy MI,
Kretzler M,
Susztak K,
Hirschhorn JN,
Florez JC,
Groop PH
GENIE Consortium
Diabetologia · 2022 · PMID 35763030 · open access
2 pages
Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes
Sandholm N,
McKnight AJ,
Salem RM,
Brennan EP,
Forsblom C,
Harjutsalo V,
Mäkinen VP,
McKay GJ,
Sadlier DM,
Williams WW,
Martin F,
Panduru NM
and 11 more — show all
Tarnow L,
Tuomilehto J,
Tryggvason K,
Zerbini G,
Comeau ME,
Langefeld CD,
Godson C,
Hirschhorn JN,
Maxwell AP,
Florez JC,
Groop PH
FIND Consortium · FinnDiane Study Group and the GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2013 · PMID 24029427
1 page
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
Ahlqvist E,
Sandholm N,
Deshmukh H,
Rayner NW,
Abdalla M,
Ladenvall C,
Ziemek D,
Fauman E,
Robertson NR,
McKeigue PM,
Valo E
and 69 more — show all
Forsblom C,
Harjutsalo V,
Perna A,
Rurali E,
Marcovecchio ML,
Igo RP Jr,
Salem RM,
Perico N,
Lajer M,
Käräjämäki A,
Imamura M,
Kubo M,
Takahashi A,
Sim X,
Liu J,
van Dam RM,
Jiang G,
Tam CHT,
Luk AOY,
Lee HM,
Lim CKP,
Szeto CC,
So WY,
Chan JCN,
Ang SF,
Dorajoo R,
Wang L,
Clara TSH,
McKnight AJ,
Duffy S,
Pezzolesi MG,
Marre M,
Gyorgy B,
Hadjadj S,
Hiraki LT,
Ahluwalia TS,
Almgren P,
Schulz CA,
Orho-Melander M,
Linneberg A,
Christensen C,
Witte DR,
Grarup N,
Brandslund I,
Melander O,
Paterson AD,
Tregouet D,
Maxwell AP,
Lim SC,
Ma RCW,
Tai ES,
Maeda S,
Lyssenko V,
Tuomi T,
Krolewski AS,
Rich SS,
Hirschhorn JN,
Florez JC,
Dunger D,
Pedersen O,
Hansen T,
Rossing P,
Remuzzi G,
Brosnan MJ,
Palmer CNA,
Groop PH,
Colhoun HM,
Groop LC,
McCarthy MI
Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group and 4 more consortia
Diabetes · 2018 · PMID 29703844
1 page
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes
Meng W,
Shah KP,
Pollack S,
Toppila I,
Hebert HL,
McCarthy MI,
Groop L,
Ahlqvist E,
Lyssenko V,
Agardh E,
Daniell M,
Kaidonis G
and 28 more — show all
Craig JE,
Mitchell P,
Liew G,
Kifley A,
Wang JJ,
Christiansen MW,
Jensen RA,
Penman A,
Hancock HA,
Chen CJ,
Correa A,
Kuo JZ,
Li X,
Chen YI,
Rotter JI,
Klein R,
Klein B,
Wong TY,
Morris AD,
Doney ASF,
Colhoun HM,
Price AL,
Burdon KP,
Groop PH,
Sandholm N,
Grassi MA,
Sobrin L,
Palmer CNA
Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Acta ophthalmologica · 2018 · PMID 30178632 · 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.