ANALYSIS OF COPY NUMBER VARIANTS (CNVS) IN A BRAZILIAN HIGH-RISK COHORT FOR PSYCHIATRIC DISORDERS

被引:0
|
作者
Santoro, Marcos [1 ]
Antonieto, Julia [1 ]
Zamariolli, Malu [1 ]
Ito, Lucas Toshio [1 ]
Pan, Pedro [1 ]
Salum, Giovanni [2 ]
Belangero, Sintia [1 ]
机构
[1] Univ Fed Sao Paulo, Sao Paulo, Brazil
[2] Univ Fed Rio Grande do Sul, Porto Alegre, RS, Brazil
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
F8
引用
收藏
页码:S224 / S224
页数:1
相关论文
共 50 条
  • [21] Copy Number Variations and Psychiatric Disorders
    Chao, Yu-Lin
    Chien, Wei-Hsien
    Liao, Hsiao-Mei
    Fang, Jye-Siung
    Chen, Chia-Hsiang
    TZU CHI MEDICAL JOURNAL, 2009, 21 (03): : 197 - 203
  • [22] The analysis of specific copy number variants (CNVs) in patient-derived neural and glial cells
    Jung, M.
    Schiller, J.
    Torenz, J.
    Gies, A.
    Klemenz, A.
    Hartmann, A.
    Giegling, I.
    Rujescu, D.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2016, 26 : S195 - S195
  • [23] Multiple heterozygous copy number variants (CNVs) with potential additive effect in patients affected by neurodevelopmental disorders (NDD)
    Servetti, M.
    Tassano, E.
    Divizia, M.
    Pisciotta, L.
    Rosti, G.
    Serio, I.
    Lerone, M.
    Cerminara, M.
    Veneselli, E.
    Nobili, L.
    Ronchetto, P.
    Puliti, A.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1858 - 1858
  • [24] Analysis of Genomic Copy Number Variation Across Psychiatric Disorders
    Klein, Marieke
    Shanta, Omar
    Hong, Oanh
    MacDonald, Jeffrey
    Thiruvahindrapuram, Bhooma
    de Pins, Agathe
    Charney, Alexander
    Letovsky, Stan Stan
    Humphrey, Jake
    Douard, Elise
    Saci, Zohra
    Jacquemont, Sebastien
    Scherer, Stephen
    Sebat, Jonathan
    BIOLOGICAL PSYCHIATRY, 2021, 89 (09) : S106 - S107
  • [25] Sequence variants and their nature in an unselected cohort of patients with high-risk myeloid disorders
    Keske, Pia
    Badbaran, Anita
    Kroeger, Nicolaus
    Christopeit, Maximilian
    BONE MARROW TRANSPLANTATION, 2019, 54 : 476 - 476
  • [26] Analysis of genomic copy number variation across psychiatric disorders
    Klein, Marieke
    Shanta, Omar
    Hong, Oanh
    MacDonald, Jeffrey
    Thiruvahindrapuram, Bhooma
    de Pins, Agathe
    Charney, Alexander
    Letovsky, Stan
    Humphrey, Jake
    Douard, Elise
    Saci, Zohra
    Jacquemont, Sebastien
    Scherer, Stephen
    Sebat, Jonathan
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2022, 30 (SUPPL 1) : 32 - 32
  • [27] COPY NUMBER VARIATION AND THEIR INTERACTION WITH POLYGENIC RISK SCORES IN PSYCHIATRIC DISORDERS
    Knowles, Emma
    Schultz, Laura
    Huguet, Guillaume
    Mollon, Josephine
    Mathias, Samuel
    Rodrigue, Amanda
    Saci, Zohra
    Douard, Elise
    Almasy, Laura
    Jacquemont, Sebastien
    Glahn, David
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2022, 63 : E42 - E43
  • [28] Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders
    Calle Sanchez, Xabier
    Helenius, Dorte
    Bybjerg-Grauholm, Jonas
    Pedersen, Carsten
    Hougaard, David M.
    Borglum, Anders D.
    Nordentoft, Merete
    Mors, Ole
    Mortensen, Preben B.
    Geschwind, Daniel H.
    Montalbano, Simone
    Raznahan, Armin
    Thompson, Wesley K.
    Ingason, Andres
    Werge, Thomas
    JAMA PSYCHIATRY, 2022, 79 (01) : 59 - 69
  • [29] ANALYSIS OF GENOMIC COPY NUMBER VARIATION AND THEIR INTERACTION WITH POLYGENIC RISK SCORES ACROSS PSYCHIATRIC DISORDERS
    Klein, Marieke
    Shanta, Omar
    Hong, Oanh
    MacDonald, Jeff
    Thiruvahindrapuram, Bhooma
    de Pins, Agathe
    Charney, Alexander
    Letovsky, Stanley
    Humphrey, Jake
    Douard, Elise
    Jacquemont, Sebastien
    Scherer, Stephen
    Sebat, Jonathan
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2021, 51 : E45 - E46
  • [30] Analysis of Mosaicism for Sequence and Copy Number Variants in a Broad Diversity of Hereditary Disorders in a Large Clinical Cohort
    Alvarez, D. Pineda
    Truty, R.
    Hambruch, T.
    Kautzer, C.
    Kennemer, M.
    Kosheleva, K.
    Kulkarni, V.
    Rhees, J.
    Stafford, A.
    Nussbaum, R.
    Aradhya, S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1153 - 1153