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; Oluf Pedersen; Matias Simons; Leif Groop; Marju Orho-Melander; Mark I. McCarthy; Olle Melander; Peter Rossing; Tuomas O. Kilpelainen; Torben Hansen

doi: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

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 GrarupOluf Pedersen, Matias Simons, Leif Groop, Marju Orho-Melander, Mark I. McCarthy, Olle Melander, Peter Rossing, Tuomas O. Kilpelainen, Torben Hansen

^*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

26 Citationer (Scopus)

109 Downloads (Pure)

Originalsprog	Engelsk
Tidsskrift	Diabetologia
Vol/bind	62
Udgave nummer	2
Sider (fra-til)	292-305
ISSN	0012-186X
DOI	https://doi.org/10.1007/s00125-018-4783-z
Status	Udgivet - 2019

Adgang til dokumentet

10.1007/s00125-018-4783-z

A novel rareCUBNvariant and three additional genes identifiedin Europeans with and without diabetes: results from an exome-wideassociation study of albuminuriaForlagets udgivne version, 1,58 MB

Citationsformater

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

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 › peer review

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

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.

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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",

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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 -