A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes

results from an exome-wide association study of albuminuria

Tarunveer S. Ahluwalia, Christina-Alexandra Schulz, Johannes Waage, Tea Skaaby, Niina Sandholm, Natalie van Zuydam, Romain Charmet, Jette Bork-Jensen, Peter Almgren, Betina H. Thuesen, Mathilda Bedin, Ivan Brandslund, Cramer K. Christensen, Allan Linneberg, Emma Ahlqvist, Per-Henrik Groop, Samy Hadjadj, David-Alexandre Tregouet, Marit E. Jorgensen, Niels Grarup & 9 muut Oluf Pedersen, Matias Simons, Leif Groop, Marju Orho-Melander, Mark I. McCarthy, Olle Melander, Peter Rossing, Tuomas O. Kilpeläinen, Torben Hansen

Tutkimustuotos: ArtikkelijulkaisuArtikkeliTieteellinenvertaisarvioitu

Alkuperäiskielienglanti
LehtiDiabetologia
Vuosikerta62
Numero2
Sivut292-305
Sivumäärä14
ISSN0012-186X
DOI - pysyväislinkit
TilaJulkaistu - helmikuuta 2019
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä, vertaisarvioitu

Tieteenalat

  • 3121 Sisätaudit
  • 3111 Biolääketieteet
  • 1184 Genetiikka, kehitysbiologia, fysiologia

Lainaa tätä

Ahluwalia, Tarunveer S. ; Schulz, Christina-Alexandra ; Waage, Johannes ; Skaaby, Tea ; Sandholm, Niina ; van Zuydam, Natalie ; Charmet, Romain ; Bork-Jensen, Jette ; Almgren, Peter ; Thuesen, Betina H. ; Bedin, Mathilda ; Brandslund, Ivan ; Christensen, Cramer K. ; Linneberg, Allan ; Ahlqvist, Emma ; Groop, Per-Henrik ; Hadjadj, Samy ; Tregouet, David-Alexandre ; Jorgensen, Marit E. ; Grarup, Niels ; Pedersen, Oluf ; Simons, Matias ; Groop, Leif ; Orho-Melander, Marju ; McCarthy, Mark I. ; Melander, Olle ; Rossing, Peter ; Kilpeläinen, Tuomas O. ; Hansen, Torben. / A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria. Julkaisussa: Diabetologia. 2019 ; Vuosikerta 62, Nro 2. Sivut 292-305.
@article{130d1b77a98840b79b18d1f11c24def8,
title = "A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria",
keywords = "Albuminuria, Diabetes, DKD, Exome chip, Genetics, Genome-wide association study, Kidney disease, GWAS, Rare variant, SKAT, Type 2 diabetes, GENOME-WIDE, KIDNEY-DISEASE, RISK, REVEALS, LOCI, METAANALYSIS, PROTECTION, RECEPTORS, DISCOVERY, FRAMEWORK, 3121 Internal medicine, 3111 Biomedicine, 1184 Genetics, developmental biology, physiology",
author = "Ahluwalia, {Tarunveer S.} and Christina-Alexandra Schulz and Johannes Waage and Tea Skaaby and Niina Sandholm and {van Zuydam}, Natalie and Romain Charmet and Jette Bork-Jensen and Peter Almgren and Thuesen, {Betina H.} and Mathilda Bedin and Ivan Brandslund and Christensen, {Cramer K.} and Allan Linneberg and Emma Ahlqvist and Per-Henrik Groop and Samy Hadjadj and David-Alexandre Tregouet and Jorgensen, {Marit E.} and Niels Grarup and Oluf Pedersen and Matias Simons and Leif Groop and Marju Orho-Melander and McCarthy, {Mark I.} and Olle Melander and Peter Rossing and Kilpel{\"a}inen, {Tuomas O.} and Torben Hansen",
year = "2019",
month = "2",
doi = "10.1007/s00125-018-4783-z",
language = "English",
volume = "62",
pages = "292--305",
journal = "Diabetologia",
issn = "0012-186X",
publisher = "Springer",
number = "2",

}

Ahluwalia, TS, Schulz, C-A, Waage, J, Skaaby, T, Sandholm, N, van Zuydam, N, Charmet, R, Bork-Jensen, J, Almgren, P, Thuesen, BH, Bedin, M, Brandslund, I, Christensen, CK, Linneberg, A, Ahlqvist, E, Groop, P-H, Hadjadj, S, Tregouet, D-A, Jorgensen, ME, Grarup, N, Pedersen, O, Simons, M, Groop, L, Orho-Melander, M, McCarthy, MI, Melander, O, Rossing, P, Kilpeläinen, TO & Hansen, T 2019, 'A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria', Diabetologia, Vuosikerta 62, Nro 2, Sivut 292-305. https://doi.org/10.1007/s00125-018-4783-z

A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria. / Ahluwalia, Tarunveer S.; Schulz, Christina-Alexandra; Waage, Johannes; Skaaby, Tea; Sandholm, Niina; van Zuydam, Natalie; Charmet, Romain; Bork-Jensen, Jette; Almgren, Peter; Thuesen, Betina H.; Bedin, Mathilda; Brandslund, Ivan; Christensen, Cramer K.; Linneberg, Allan; Ahlqvist, Emma; Groop, Per-Henrik; Hadjadj, Samy; Tregouet, David-Alexandre; Jorgensen, Marit E.; Grarup, Niels; Pedersen, Oluf; Simons, Matias; Groop, Leif; Orho-Melander, Marju; McCarthy, Mark I.; Melander, Olle; Rossing, Peter; Kilpeläinen, Tuomas O.; Hansen, Torben.

julkaisussa: Diabetologia, Vuosikerta 62, Nro 2, 02.2019, s. 292-305.

Tutkimustuotos: ArtikkelijulkaisuArtikkeliTieteellinenvertaisarvioitu

TY - JOUR

T1 - A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes

T2 - results from an exome-wide association study of albuminuria

AU - Ahluwalia, Tarunveer S.

AU - Schulz, Christina-Alexandra

AU - Waage, Johannes

AU - Skaaby, Tea

AU - Sandholm, Niina

AU - van Zuydam, Natalie

AU - Charmet, Romain

AU - Bork-Jensen, Jette

AU - Almgren, Peter

AU - Thuesen, Betina H.

AU - Bedin, Mathilda

AU - Brandslund, Ivan

AU - Christensen, Cramer K.

AU - Linneberg, Allan

AU - Ahlqvist, Emma

AU - Groop, Per-Henrik

AU - Hadjadj, Samy

AU - Tregouet, David-Alexandre

AU - Jorgensen, Marit E.

AU - Grarup, Niels

AU - Pedersen, Oluf

AU - Simons, Matias

AU - Groop, Leif

AU - Orho-Melander, Marju

AU - McCarthy, Mark I.

AU - Melander, Olle

AU - Rossing, Peter

AU - Kilpeläinen, Tuomas O.

AU - Hansen, Torben

PY - 2019/2

Y1 - 2019/2

KW - Albuminuria

KW - Diabetes

KW - DKD

KW - Exome chip

KW - Genetics

KW - Genome-wide association study

KW - Kidney disease

KW - GWAS

KW - Rare variant

KW - SKAT

KW - Type 2 diabetes

KW - GENOME-WIDE

KW - KIDNEY-DISEASE

KW - RISK

KW - REVEALS

KW - LOCI

KW - METAANALYSIS

KW - PROTECTION

KW - RECEPTORS

KW - DISCOVERY

KW - FRAMEWORK

KW - 3121 Internal medicine

KW - 3111 Biomedicine

KW - 1184 Genetics, developmental biology, physiology

U2 - 10.1007/s00125-018-4783-z

DO - 10.1007/s00125-018-4783-z

M3 - Article

VL - 62

SP - 292

EP - 305

JO - Diabetologia

JF - Diabetologia

SN - 0012-186X

IS - 2

ER -