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2,677 papers hold this site up. Every variant and condition page names
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145 matches for
He G,
showing the first 20.
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
Overexpression of the Cytokine BAFF and Autoimmunity Risk
Steri M,
Orrù V,
Idda ML,
Pitzalis M,
Pala M,
Zara I,
Sidore C,
Faà V,
Floris M,
Deiana M,
Asunis I,
Porcu E
and 69 more — show all
Mulas A,
Piras MG,
Lobina M,
Lai S,
Marongiu M,
Serra V,
Marongiu M,
Sole G,
Busonero F,
Maschio A,
Cusano R,
Cuccuru G,
Deidda F,
Poddie F,
Farina G,
Dei M,
Virdis F,
Olla S,
Satta MA,
Pani M,
Delitala A,
Cocco E,
Frau J,
Coghe G,
Lorefice L,
Fenu G,
Ferrigno P,
Ban M,
Barizzone N,
Leone M,
Guerini FR,
Piga M,
Firinu D,
Kockum I,
Lima Bomfim I,
Olsson T,
Alfredsson L,
Suarez A,
Carreira PE,
Castillo-Palma MJ,
Marcus JH,
Congia M,
Angius A,
Melis M,
Gonzalez A,
Alarcón Riquelme ME,
da Silva BM,
Marchini M,
Danieli MG,
Del Giacco S,
Mathieu A,
Pani A,
Montgomery SB,
Rosati G,
Hillert J,
Sawcer S,
D'Alfonso S,
Todd JA,
Novembre J,
Abecasis GR,
Whalen MB,
Marrosu MG,
Meloni A,
Sanna S,
Gorospe M,
Schlessinger D,
Fiorillo E,
Zoledziewska M,
Cucca F
The New England journal of medicine · 2017 · PMID 28445677
1 page
Genetic variation in the gene <i>LRP2</i> increases relapse risk in multiple sclerosis
Zhou Y,
Graves JS,
Simpson S Jr,
Charlesworth JC,
Mei IV,
Waubant E,
Barcellos LF,
Belman A,
Krupp L,
Lucas R,
Ponsonby AL,
Taylor BV
Ausimmmune/AusLong investigators group
Journal of neurology, neurosurgery, and psychiatry · 2017 · PMID 28739605
1 page
The nature of nurture: Effects of parental genotypes
Kong A,
Thorleifsson G,
Frigge ML,
Vilhjalmsson BJ,
Young AI,
Thorgeirsson TE,
Benonisdottir S,
Oddsson A,
Halldorsson BV,
Masson G,
Gudbjartsson DF,
Helgason A
and 3 more — show all
Science (New York, N.Y.) · 2018 · PMID 29371463
1 page
Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population
Grarup N,
Moltke I,
Andersen MK,
Bjerregaard P,
Larsen CVL,
Dahl-Petersen IK,
Jørsboe E,
Tiwari HK,
Hopkins SE,
Wiener HW,
Boyer BB,
Linneberg A
and 4 more — show all
Diabetologia · 2018 · PMID 29926116 · open access
1 page
Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy
Schoeler NE,
Leu C,
Balestrini S,
Mudge JM,
Steward CA,
Frankish A,
Leung MA,
Mackay M,
Scheffer I,
Williams R,
Sander JW,
Cross JH
and 1 more — show all
Epilepsia · 2018 · PMID 30009487
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
Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci
Gong J,
Wang F,
Xiao B,
Panjwani N,
Lin F,
Keenan K,
Avolio J,
Esmaeili M,
Zhang L,
He G,
Soave D,
Mastromatteo S
and 12 more — show all
Baskurt Z,
Kim S,
O'Neal WK,
Polineni D,
Blackman SM,
Corvol H,
Cutting GR,
Drumm M,
Knowles MR,
Rommens JM,
Sun L,
Strug LJ
PLoS genetics · 2019 · PMID 30807572 · open access
1 page
Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism
Pardiñas AF,
Nalmpanti M,
Pocklington AJ,
Legge SE,
Medway C,
King A,
Jansen J,
Helthuis M,
Zammit S,
MacCabe J,
Owen MJ,
O'Donovan MC
and 1 more — show all
The American journal of psychiatry · 2019 · PMID 30922102
1 page
Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study
Zhao SX,
Liu W,
Liang J,
Gao GQ,
Zhang XM,
Yao Y,
Wang HN,
Yuan FF,
Xue LQ,
Ma YR,
Zhang LL,
Ye XP
and 25 more — show all
Zhang QY,
Sun F,
Zhang RJ,
Yang SY,
Zhan M,
Du WH,
Liu BL,
Chen X,
Song ZY,
Li XS,
Li P,
Ru Y,
Zuo CL,
Li SX,
Han B,
Zhu H,
Qiao J,
Xuan M,
Su B,
Sun F,
Ma JH,
Chen JL,
Tian HM,
Chen SJ,
Song HD
China Consortium for the Genetics of Autoimmune Thyroid Disease
JAMA network open · 2019 · PMID 31050781 · open access
1 page
Defining the genetic control of human blood plasma N-glycome using genome-wide association study
Sharapov SZ,
Tsepilov YA,
Klaric L,
Mangino M,
Thareja G,
Shadrina AS,
Simurina M,
Dagostino C,
Dmitrieva J,
Vilaj M,
Vuckovic F,
Pavic T
and 20 more — show all
Stambuk J,
Stambuk J,
Trbojevic-Akmacic I,
Kristic J,
Simunovic J,
Momcilovic A,
Campbell H,
Doherty M,
Dunlop MG,
Farrington SM,
Pucic-Bakovic M,
Gieger C,
Allegri M,
Louis E,
Georges M,
Suhre K,
Spector T,
Williams FMK,
Lauc G,
Aulchenko YS
Human molecular genetics · 2019 · PMID 31163085
1 page
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Bandres-Ciga S,
Ahmed S,
Sabir MS,
Blauwendraat C,
Adarmes-Gómez AD,
Bernal-Bernal I,
Bonilla-Toribio M,
Buiza-Rueda D,
Carrillo F,
Carrión-Claro M,
Gómez-Garre P,
Jesús S
and 83 more — show all
Labrador-Espinosa MA,
Macias D,
Méndez-Del-Barrio C,
Periñán-Tocino T,
Tejera-Parrado C,
Vargas-González L,
Diez-Fairen M,
Alvarez I,
Tartari JP,
Buongiorno M,
Aguilar M,
Gorostidi A,
Bergareche JA,
Mondragon E,
Vinagre-Aragon A,
Croitoru I,
Ruiz-Martínez J,
Dols-Icardo O,
Kulisevsky J,
Marín-Lahoz J,
Pagonabarraga J,
Pascual-Sedano B,
Ezquerra M,
Cámara A,
Compta Y,
Fernández M,
Fernández-Santiago R,
Muñoz E,
Tolosa E,
Valldeoriola F,
Gonzalez-Aramburu I,
Sanchez Rodriguez A,
Sierra M,
Menéndez-González M,
Blazquez M,
Garcia C,
Suarez-San Martin E,
García-Ruiz P,
Martínez-Castrillo JC,
Vela-Desojo L,
Ruz C,
Barrero FJ,
Escamilla-Sevilla F,
Mínguez-Castellanos A,
Cerdan D,
Tabernero C,
Gomez Heredia MJ,
Perez Errazquin F,
Romero-Acebal M,
Feliz C,
Lopez-Sendon JL,
Mata M,
Martínez Torres I,
Kim JJ,
Dalgard CL,
Brooks J,
Saez-Atienzar S,
Gibbs JR,
Jorda R,
Botia JA,
Bonet-Ponce L,
Morrison KE,
Clarke C,
Tan M,
Morris H,
Edsall C,
Hernandez D,
Simon-Sanchez J,
Nalls MA,
Scholz SW,
Jimenez-Escrig A,
Duarte J,
Vives F,
Duran R,
Hoenicka J,
Alvarez V,
Infante J,
Marti MJ,
Clarimón J,
López de Munain A,
Pastor P,
Mir P,
Singleton A
American Genome Center · International Parkinson Disease Genomics Consortium
Movement disorders : official journal of the Movement Disorder Society · 2019 · PMID 31660654
1 page
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Xie J,
Liu L,
Mladkova N,
Li Y,
Ren H,
Wang W,
Cui Z,
Lin L,
Hu X,
Yu X,
Xu J,
Liu G
and 108 more — show all
Caliskan Y,
Sidore C,
Balderes O,
Rosen RJ,
Bodria M,
Zanoni F,
Zhang JY,
Krithivasan P,
Mehl K,
Marasa M,
Khan A,
Ozay F,
Canetta PA,
Bomback AS,
Appel GB,
Sanna-Cherchi S,
Sampson MG,
Mariani LH,
Perkowska-Ptasinska A,
Durlik M,
Mucha K,
Moszczuk B,
Foroncewicz B,
Pączek L,
Habura I,
Ars E,
Ballarin J,
Mani LY,
Vogt B,
Ozturk S,
Yildiz A,
Seyahi N,
Arikan H,
Koc M,
Basturk T,
Karahan G,
Akgul SU,
Sever MS,
Zhang D,
Santoro D,
Bonomini M,
Londrino F,
Gesualdo L,
Reiterova J,
Tesar V,
Izzi C,
Savoldi S,
Spotti D,
Marcantoni C,
Messa P,
Galliani M,
Roccatello D,
Granata S,
Zaza G,
Lugani F,
Ghiggeri G,
Pisani I,
Allegri L,
Sprangers B,
Park JH,
Cho B,
Kim YS,
Kim DK,
Suzuki H,
Amoroso A,
Cattran DC,
Fervenza FC,
Pani A,
Hamilton P,
Harris S,
Gupta S,
Cheshire C,
Dufek S,
Issler N,
Pepper RJ,
Connolly J,
Powis S,
Bockenhauer D,
Stanescu HC,
Ashman N,
Loos RJF,
Kenny EE,
Wuttke M,
Eckardt KU,
Köttgen A,
Hofstra JM,
Coenen MJH,
Kiemeney LA,
Akilesh S,
Kretzler M,
Beck LH,
Stengel B,
Debiec H,
Ronco P,
Wetzels JFM,
Zoledziewska M,
Cucca F,
Ionita-Laza I,
Lee H,
Hoxha E,
Stahl RAK,
Brenchley P,
Scolari F,
Zhao MH,
Gharavi AG,
Kleta R,
Chen N,
Kiryluk K
Nature communications · 2020 · PMID 32231244 · open access
1 page
Genome-wide association study of cardiac troponin I in the general population
Moksnes MR,
Røsjø H,
Richmond A,
Lyngbakken MN,
Graham SE,
Hansen AF,
Wolford BN,
Gagliano Taliun SA,
LeFaive J,
Rasheed H,
Thomas LF,
Zhou W
and 18 more — show all
Aung N,
Surakka I,
Douville NJ,
Campbell A,
Porteous DJ,
Petersen SE,
Munroe PB,
Welsh P,
Sattar N,
Smith GD,
Fritsche LG,
Nielsen JB,
Åsvold BO,
Hveem K,
Hayward C,
Willer CJ,
Brumpton BM,
Omland T
Human molecular genetics · 2021 · PMID 33961016 · open access
1 page
Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population
de Haan A,
Ahmadizar F,
van der Most PJ,
Thio CHL,
Kamali Z,
Ani A,
Ghanbari M,
Chaker L,
van Meurs J,
Ikram MK,
van Goor H,
Bakker SJL
and 6 more — show all
Frontiers in cardiovascular medicine · 2021 · PMID 35097025 · open access
1 page
Genetics of osteopontin in patients with chronic kidney disease: The German Chronic Kidney Disease study
Cheng Y,
Li Y,
Scherer N,
Grundner-Culemann F,
Lehtimäki T,
Mishra BH,
Raitakari OT,
Nauck M,
Eckardt KU,
Sekula P,
Schultheiss UT
GCKD investigators
PLoS genetics · 2022 · PMID 35385482 · 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.