Erratum: Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086))

Kirk E. Lohmueller; Thomas Sparsø; Qibin Li; Ehm Andersson; Thorfinn Korneliussen; Anders Albrechtsen; Karina Banasik; Niels Grarup; Ingileif Hallgrimsdottir; Kristoffer Kiil; Tuomas O. Kilpeläinen; Nikolaj T. Krarup; Tune H. Pers; Gaston Sanchez; Youna Hu; Michael Degiorgio; Torben Jørgensen; Annelli Sandbæk; Torsten Lauritzen; Søren Brunak; Karsten Kristiansen; Yingrui Li; Torben Hansen; Jun Wang; Rasmus Nielsen; Oluf Pedersen

doi:10.1016/j.ajhg.2014.02.002

Erratum: Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086))

Kirk E. Lohmueller, Thomas Sparsø, Qibin Li, Ehm Andersson, Thorfinn Korneliussen, Anders Albrechtsen, Karina Banasik, Niels Grarup, Ingileif Hallgrimsdottir, Kristoffer Kiil, Tuomas O. Kilpeläinen, Nikolaj T. Krarup, Tune H. Pers, Gaston Sanchez, Youna Hu, Michael Degiorgio, Torben Jørgensen, Annelli Sandbæk, Torsten Lauritzen, Søren BrunakKarsten Kristiansen, Yingrui Li, Torben Hansen, Jun Wang, Rasmus Nielsen, Oluf Pedersen

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English (US)
Pages (from-to)	479
Number of pages	1
Journal	American Journal of Human Genetics
Volume	94
Issue number	3
DOIs	https://doi.org/10.1016/j.ajhg.2014.02.002
State	Published - Mar 6 2014

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

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10.1016/j.ajhg.2014.02.002

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Lohmueller, K. E., Sparsø, T., Li, Q., Andersson, E., Korneliussen, T., Albrechtsen, A., Banasik, K., Grarup, N., Hallgrimsdottir, I., Kiil, K., Kilpeläinen, T. O., Krarup, N. T., Pers, T. H., Sanchez, G., Hu, Y., Degiorgio, M., Jørgensen, T., Sandbæk, A., Lauritzen, T., ... Pedersen, O. (2014). Erratum: Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086)). American Journal of Human Genetics, 94(3), 479. https://doi.org/10.1016/j.ajhg.2014.02.002

Lohmueller, Kirk E. ; Sparsø, Thomas ; Li, Qibin ; Andersson, Ehm ; Korneliussen, Thorfinn ; Albrechtsen, Anders ; Banasik, Karina ; Grarup, Niels ; Hallgrimsdottir, Ingileif ; Kiil, Kristoffer ; Kilpeläinen, Tuomas O. ; Krarup, Nikolaj T. ; Pers, Tune H. ; Sanchez, Gaston ; Hu, Youna ; Degiorgio, Michael ; Jørgensen, Torben ; Sandbæk, Annelli ; Lauritzen, Torsten ; Brunak, Søren ; Kristiansen, Karsten ; Li, Yingrui ; Hansen, Torben ; Wang, Jun ; Nielsen, Rasmus ; Pedersen, Oluf. / Erratum : Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086)). In: American Journal of Human Genetics. 2014 ; Vol. 94, No. 3. pp. 479.

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author = "Lohmueller, {Kirk E.} and Thomas Spars{\o} and Qibin Li and Ehm Andersson and Thorfinn Korneliussen and Anders Albrechtsen and Karina Banasik and Niels Grarup and Ingileif Hallgrimsdottir and Kristoffer Kiil and Kilpel{\"a}inen, {Tuomas O.} and Krarup, {Nikolaj T.} and Pers, {Tune H.} and Gaston Sanchez and Youna Hu and Michael Degiorgio and Torben J{\o}rgensen and Annelli Sandb{\ae}k and Torsten Lauritzen and S{\o}ren Brunak and Karsten Kristiansen and Yingrui Li and Torben Hansen and Jun Wang and Rasmus Nielsen and Oluf Pedersen",

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doi = "10.1016/j.ajhg.2014.02.002",

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Lohmueller, KE, Sparsø, T, Li, Q, Andersson, E, Korneliussen, T, Albrechtsen, A, Banasik, K, Grarup, N, Hallgrimsdottir, I, Kiil, K, Kilpeläinen, TO, Krarup, NT, Pers, TH, Sanchez, G, Hu, Y, Degiorgio, M, Jørgensen, T, Sandbæk, A, Lauritzen, T, Brunak, S, Kristiansen, K, Li, Y, Hansen, T, Wang, J, Nielsen, R & Pedersen, O 2014, 'Erratum: Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086))', American Journal of Human Genetics, vol. 94, no. 3, pp. 479. https://doi.org/10.1016/j.ajhg.2014.02.002

Erratum : Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086)). / Lohmueller, Kirk E.; Sparsø, Thomas; Li, Qibin; Andersson, Ehm; Korneliussen, Thorfinn; Albrechtsen, Anders; Banasik, Karina; Grarup, Niels; Hallgrimsdottir, Ingileif; Kiil, Kristoffer; Kilpeläinen, Tuomas O.; Krarup, Nikolaj T.; Pers, Tune H.; Sanchez, Gaston; Hu, Youna; Degiorgio, Michael; Jørgensen, Torben; Sandbæk, Annelli; Lauritzen, Torsten; Brunak, Søren; Kristiansen, Karsten; Li, Yingrui; Hansen, Torben; Wang, Jun; Nielsen, Rasmus; Pedersen, Oluf.

In: American Journal of Human Genetics, Vol. 94, No. 3, 06.03.2014, p. 479.

Research output: Contribution to journal › Comment/debate › peer-review

TY - JOUR

T1 - Erratum

T2 - Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086))

AU - Lohmueller, Kirk E.

AU - Sparsø, Thomas

AU - Li, Qibin

AU - Andersson, Ehm

AU - Korneliussen, Thorfinn

AU - Albrechtsen, Anders

AU - Banasik, Karina

AU - Grarup, Niels

AU - Hallgrimsdottir, Ingileif

AU - Kiil, Kristoffer

AU - Kilpeläinen, Tuomas O.

AU - Krarup, Nikolaj T.

AU - Pers, Tune H.

AU - Sanchez, Gaston

AU - Hu, Youna

AU - Degiorgio, Michael

AU - Jørgensen, Torben

AU - Sandbæk, Annelli

AU - Lauritzen, Torsten

AU - Brunak, Søren

AU - Kristiansen, Karsten

AU - Li, Yingrui

AU - Hansen, Torben

AU - Wang, Jun

AU - Nielsen, Rasmus

AU - Pedersen, Oluf

PY - 2014/3/6

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U2 - 10.1016/j.ajhg.2014.02.002

DO - 10.1016/j.ajhg.2014.02.002

M3 - Comment/debate

AN - SCOPUS:84896764202

VL - 94

SP - 479

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

SN - 0002-9297

IS - 3

ER -

Erratum: Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes (The American Journal of Human Genetics (2013) 93 (1072-1086))

All Science Journal Classification (ASJC) codes

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