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Sequence analysis of 17 NRXN1 deletions. / Hoeffding, Louise Kristine Enggaard; Hansen, Thomas; Ingason, Andrés; Doung, Linh; Thygesen, Johan H; Møller, Rikke S; Tommerup, Niels; Kirov, George; Rujescu, Dan; Larsen, Lars A; Werge, Thomas.
I:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, Bind 165, Nr. 1, 01.2014, s. 52-61.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Hoeffding, LKE, Hansen, T, Ingason, A, Doung, L, Thygesen, JH, Møller, RS
, Tommerup, N, Kirov, G, Rujescu, D
, Larsen, LA & Werge, T 2014, '
Sequence analysis of 17 NRXN1 deletions',
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, bind 165, nr. 1, s. 52-61.
https://doi.org/10.1002/ajmg.b.32204APA
Hoeffding, L. K. E., Hansen, T., Ingason, A., Doung, L., Thygesen, J. H., Møller, R. S.
, Tommerup, N., Kirov, G., Rujescu, D.
, Larsen, L. A., & Werge, T. (2014).
Sequence analysis of 17 NRXN1 deletions.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics,
165(1), 52-61.
https://doi.org/10.1002/ajmg.b.32204Vancouver
Hoeffding LKE, Hansen T, Ingason A, Doung L, Thygesen JH, Møller RS o.a.
Sequence analysis of 17 NRXN1 deletions.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 2014 jan.;165(1):52-61.
https://doi.org/10.1002/ajmg.b.32204Author
Hoeffding, Louise Kristine Enggaard ; Hansen, Thomas ; Ingason, Andrés ; Doung, Linh ; Thygesen, Johan H ; Møller, Rikke S ; Tommerup, Niels ; Kirov, George ; Rujescu, Dan ; Larsen, Lars A ; Werge, Thomas. / Sequence analysis of 17 NRXN1 deletions. I: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 2014 ; Bind 165, Nr. 1. s. 52-61.
Bibtex
@article{484d428a1a2d402b90a26eac939d0ab9,
title = "Sequence analysis of 17 NRXN1 deletions",
abstract = "Genome instability plays fundamental roles in human evolution and phenotypic variation within our population. This instability leads to genomic rearrangements that are involved in a wide variety of human disorders, including congenital and neurodevelopmental disorders, and cancers. Insight into the molecular mechanisms governing such genomic rearrangements may increase our understanding of disease pathology and evolutionary processes. Here we analyse 17 carriers of non-recurrent deletions in the NRXN1 gene, which have been associated with neurodevelopmental disorders, e.g. schizophrenia, autism and epilepsies.",
author = "Hoeffding, {Louise Kristine Enggaard} and Thomas Hansen and Andr{\'e}s Ingason and Linh Doung and Thygesen, {Johan H} and M{\o}ller, {Rikke S} and Niels Tommerup and George Kirov and Dan Rujescu and Larsen, {Lars A} and Thomas Werge",
note = "{\textcopyright} 2013 Wiley Periodicals, Inc.",
year = "2014",
month = jan,
doi = "10.1002/ajmg.b.32204",
language = "English",
volume = "165",
pages = "52--61",
journal = "American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics",
issn = "1552-4841",
publisher = "JohnWiley & Sons, Inc.",
number = "1",
}
RIS
TY - JOUR
T1 - Sequence analysis of 17 NRXN1 deletions
AU - Hoeffding, Louise Kristine Enggaard
AU - Hansen, Thomas
AU - Ingason, Andrés
AU - Doung, Linh
AU - Thygesen, Johan H
AU - Møller, Rikke S
AU - Tommerup, Niels
AU - Kirov, George
AU - Rujescu, Dan
AU - Larsen, Lars A
AU - Werge, Thomas
N1 - © 2013 Wiley Periodicals, Inc.
PY - 2014/1
Y1 - 2014/1
N2 - Genome instability plays fundamental roles in human evolution and phenotypic variation within our population. This instability leads to genomic rearrangements that are involved in a wide variety of human disorders, including congenital and neurodevelopmental disorders, and cancers. Insight into the molecular mechanisms governing such genomic rearrangements may increase our understanding of disease pathology and evolutionary processes. Here we analyse 17 carriers of non-recurrent deletions in the NRXN1 gene, which have been associated with neurodevelopmental disorders, e.g. schizophrenia, autism and epilepsies.
AB - Genome instability plays fundamental roles in human evolution and phenotypic variation within our population. This instability leads to genomic rearrangements that are involved in a wide variety of human disorders, including congenital and neurodevelopmental disorders, and cancers. Insight into the molecular mechanisms governing such genomic rearrangements may increase our understanding of disease pathology and evolutionary processes. Here we analyse 17 carriers of non-recurrent deletions in the NRXN1 gene, which have been associated with neurodevelopmental disorders, e.g. schizophrenia, autism and epilepsies.
U2 - 10.1002/ajmg.b.32204
DO - 10.1002/ajmg.b.32204
M3 - Journal article
C2 - 24339137
VL - 165
SP - 52
EP - 61
JO - American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
JF - American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics
SN - 1552-4841
IS - 1
ER -
