Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

Linh T. T. Duong; Louise K. Hoeffding; Kirsten B. Petersen; Charlotte D. Knudsen; Johan H. Thygesen; Laura L. Klitten; Niels Tommerup; Andres Ingason; Thomas Werge

doi:10.1016/j.ejmg.2015.11.004

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

Linh T. T. Duong, Louise K. Hoeffding, Kirsten B. Petersen, Charlotte D. Knudsen, Johan H. Thygesen, Laura L. Klitten, Niels Tommerup, Andres Ingason, Thomas Werge

9 Citations (Scopus)

Original language	English
Journal	European Journal of Medical Genetics
Volume	58
Issue number	12
Pages (from-to)	650-653
Number of pages	4
ISSN	1769-7212
DOIs	https://doi.org/10.1016/j.ejmg.2015.11.004
Publication status	Published - Dec 2015

Keywords

Deletions
2p16.3 (NRXN1) deletion
15q11.2 deletion
Schizophrenia
Family study
AK127244
Non-coding regions

Access to Document

10.1016/j.ejmg.2015.11.004

Cite this

Duong, L. T. T., Hoeffding, L. K., Petersen, K. B., Knudsen, C. D., Thygesen, J. H., Klitten, L. L., Tommerup, N., Ingason, A., & Werge, T. (2015). Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family. European Journal of Medical Genetics, 58(12), 650-653. https://doi.org/10.1016/j.ejmg.2015.11.004

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family. / Duong, Linh T. T.; Hoeffding, Louise K.; Petersen, Kirsten B. et al.

In: European Journal of Medical Genetics, Vol. 58, No. 12, 12.2015, p. 650-653.

Research output: Contribution to journal › Journal article › Research › peer-review

Duong, LTT, Hoeffding, LK, Petersen, KB, Knudsen, CD, Thygesen, JH, Klitten, LL, Tommerup, N, Ingason, A & Werge, T 2015, 'Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family', European Journal of Medical Genetics, vol. 58, no. 12, pp. 650-653. https://doi.org/10.1016/j.ejmg.2015.11.004

@article{ea53c663ce91411a93133831bf76a2d6,

title = "Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family",

keywords = "Deletions, 2p16.3 (NRXN1) deletion, 15q11.2 deletion, Schizophrenia, Family study, AK127244, Non-coding regions",

author = "Duong, {Linh T. T.} and Hoeffding, {Louise K.} and Petersen, {Kirsten B.} and Knudsen, {Charlotte D.} and Thygesen, {Johan H.} and Klitten, {Laura L.} and Niels Tommerup and Andres Ingason and Thomas Werge",

year = "2015",

month = dec,

doi = "10.1016/j.ejmg.2015.11.004",

language = "English",

volume = "58",

pages = "650--653",

journal = "European Journal of Medical Genetics",

issn = "1769-7212",

publisher = "Elsevier Masson",

number = "12",

}

TY - JOUR

T1 - Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

AU - Duong, Linh T. T.

AU - Hoeffding, Louise K.

AU - Petersen, Kirsten B.

AU - Knudsen, Charlotte D.

AU - Thygesen, Johan H.

AU - Klitten, Laura L.

AU - Tommerup, Niels

AU - Ingason, Andres

AU - Werge, Thomas

PY - 2015/12

Y1 - 2015/12

KW - Deletions

KW - 2p16.3 (NRXN1) deletion

KW - 15q11.2 deletion

KW - Schizophrenia

KW - Family study

KW - AK127244

KW - Non-coding regions

U2 - 10.1016/j.ejmg.2015.11.004

DO - 10.1016/j.ejmg.2015.11.004

M3 - Journal article

C2 - 26563496

SN - 1769-7212

VL - 58

SP - 650

EP - 653

JO - European Journal of Medical Genetics

JF - European Journal of Medical Genetics

IS - 12

ER -

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

Keywords

Access to Document

Fingerprint

Cite this