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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; Kilpelainen, Tuomas O.; Hansen, Torben.
I:
Diabetologia, Bind 62, Nr. 2, 2019, s. 292-305.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
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, Kilpelainen, 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, bind 62, nr. 2, s. 292-305.
https://doi.org/10.1007/s00125-018-4783-z
APA
Ahluwalia, T. S., Schulz, C-A., Waage, J., Skaaby, T., Sandholm, N., van Zuydam, N., Charmet, R., Bork-Jensen, J., Almgren, P., Thuesen, B. H., Bedin, M., Brandslund, I., Christensen, C. K.
, Linneberg, A., Ahlqvist, E., Groop, P-H., Hadjadj, S., Tregouet, D-A., Jorgensen, M. E.
, ... 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,
62(2), 292-305.
https://doi.org/10.1007/s00125-018-4783-z
Vancouver
Ahluwalia TS, Schulz C-A, Waage J, Skaaby T, Sandholm N, van Zuydam N o.a.
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. 2019;62(2):292-305.
https://doi.org/10.1007/s00125-018-4783-z
Author
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 ; Kilpelainen, 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. I: Diabetologia. 2019 ; Bind 62, Nr. 2. s. 292-305.
Bibtex
@article{3888d6bce0784903af55ee38a8d952ab,
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",
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 Kilpelainen, {Tuomas O.} and Torben Hansen",
year = "2019",
doi = "10.1007/s00125-018-4783-z",
language = "English",
volume = "62",
pages = "292--305",
journal = "Diabetologia",
issn = "0012-186X",
publisher = "Springer",
number = "2",
}
RIS
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 - Kilpelainen, Tuomas O.
AU - Hansen, Torben
PY - 2019
Y1 - 2019
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
U2 - 10.1007/s00125-018-4783-z
DO - 10.1007/s00125-018-4783-z
M3 - Journal article
C2 - 30547231
VL - 62
SP - 292
EP - 305
JO - Diabetologia
JF - Diabetologia
SN - 0012-186X
IS - 2
ER -