[HTML][HTML] Genome-wide association study reveals two new risk loci for bipolar disorder

…, M Bauer, M Hautzinger, S Moebus, L Priebe… - Nature …, 2014 - nature.com
Bipolar disorder (BD) is a common and highly heritable mental illness and genome-wide
association studies (GWAS) have robustly identified the first common genetic variants involved …

[PDF][PDF] Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

…, C Meesters, S Herms, M Weingarten, L Priebe… - The American Journal of …, 2011 - cell.com
We conducted a genome-wide association study (GWAS) and a follow-up study of bipolar
disorder (BD), a common neuropsychiatric disorder. In the GWAS, we investigated 499,494 …

The complement control-related genes CSMD1 and CSMD2 associate to schizophrenia

…, TW Mühleisen, F Degenhardt, L Priebe… - Biological …, 2011 - Elsevier
BACKGROUND: Patients with schizophrenia often suffer from cognitive dysfunction, including
impaired learning and memory. We recently demonstrated that long-term potentiation in …

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

…, DM Hougaard, T Ørntoft, P Kapelski, L Priebe… - Molecular …, 2012 - nature.com
Recent molecular studies have implicated common alleles of small to moderate effect and
rare alleles with larger effect sizes in the genetic architecture of schizophrenia (SCZ). It is …

[HTML][HTML] Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity

…, S Wohlfart, M Zweier, S Uebe, L Priebe… - European Journal of …, 2011 - nature.com
Non-specific intellectual disability of autosomal recessive inheritance (NS-ARID) represents
an important fraction of severe cognitive dysfunction disorders. To date, only 10 genes have …

Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

…, V Srikanth, J Lahti, HJ Grabe, JA Smith, L Priebe… - Biological …, 2015 - Elsevier
Background Memory performance in older persons can reflect genetic influences on cognitive
function and dementing processes. We aimed to identify genetic contributions to verbal …

[HTML][HTML] DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations

…, MA Jamil, N Nuesgen, F Schreiner, L Priebe… - Clinical …, 2015 - Springer
Background Abnormal sex chromosome numbers in humans are observed in Turner (45,X)
and Klinefelter (47,XXY) syndromes. Both syndromes are associated with several clinical …

Implication of a rare deletion at distal 16p11. 2 in schizophrenia

…, MM Nöthen, F Degenhardt, L Priebe… - JAMA …, 2013 - jamanetwork.com
Context Large genomic copy number variations have been implicated as strong risk factors
for schizophrenia. However, the rarity of these events has created challenges for the …

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

…, J Strohmaier, F Degenhardt, L Priebe… - Schizophrenia …, 2012 - Elsevier
A recent study found genome-wide significant association between common variation in the
gene neurocan (NCAN, rs1064395) and bipolar disorder (BD). In view of accumulating …

Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature

…, S Hosie, S Holland-Cunz, L Priebe… - European journal of …, 2011 - Springer
Introduction Anorectal malformations (ARM) range from mild anal to severe anorectal
anomalies. Approximately 50% are estimated to be non-syndromic with multiple familial cases …