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 for this work

Department of Clinical Medicine

12 Citations (Scopus)

19 Downloads (Pure)

Original language	English
Journal	Diabetologia
Volume	62
Issue number	2
Pages (from-to)	292-305
ISSN	0012-186X
DOIs	https://doi.org/10.1007/s00125-018-4783-z
Publication status	Published - 1 Feb 2019

Keywords

Albuminuria
Diabetes
DKD
Exome chip
Genetics
Genome-wide association study
Kidney disease
GWAS
Rare variant
SKAT
Type 2 diabetes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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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 albuminuriaFinal published version, 1.58 MB

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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 et al.
In: Diabetologia, Vol. 62, No. 2, 01.02.2019, p. 292-305.

Research output: Contribution to journal › Journal article › Research › 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, vol. 62, no. 2, pp. 292-305. https://doi.org/10.1007/s00125-018-4783-z

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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 - 2019/2/1

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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

SN - 0012-186X

VL - 62

SP - 292

EP - 305

JO - Diabetologia

JF - Diabetologia

IS - 2

ER -

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

UN SDGs

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