Genetic study of NRXN1β variants in Spanish patients with schizophrenia

被引:0
|
作者
Abasolo, Nerea [1 ]
Roig, Barbara [1 ]
Martorell, Lourdes [1 ]
Martinez-Leal, Rafael [2 ]
Aguilera, Francisco [2 ]
Jesus Camacho-Garcia, Rafael [3 ]
Orejuela, Carmen [2 ]
Scholl, Francisco G. [3 ,4 ]
Martinez-Mir, Amalia [3 ]
Vilella, Elisabet [1 ]
机构
[1] Univ Rovira & Virgili, Hosp Univ Inst Pere Mata, IISPV, CIBERSAM, E-43201 Reus, Spain
[2] Univ Rovira & Virgili, Fundacio Villablanca, IISPV, CIBERSAM, E-43201 Reus, Spain
[3] Hosp Univ Virgen del Rocio CSIC Univ Sevilla, Inst Biomed Sevilla IBiS, Seville, Spain
[4] Univ Seville, Fac Med, Dept Fisiol Med & Biofis, Seville, Spain
关键词
DELETIONS; AUTISM; NEUREXIN-1-BETA;
D O I
10.1016/j.schres.2014.09.002
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
引用
收藏
页码:554 / 555
页数:2
相关论文
共 50 条
  • [1] Rare NRXN1 promoter variants in patients with schizophrenia
    Shah, Abhishek K.
    Tioleco, Nina M.
    Nolan, Karen
    Locker, Joseph
    Groh, Katherine
    Villa, Catalina
    Stopkova, Pavla
    Pedrosa, Erika
    Lachman, Herbert M.
    NEUROSCIENCE LETTERS, 2010, 475 (02) : 80 - 84
  • [2] Neurexin 1 (NRXN1) Deletions in Schizophrenia
    Kirov, George
    Rujescu, Dan
    Ingason, Andres
    Collier, David A.
    O'Donovan, Michael C.
    Owen, Michael J.
    SCHIZOPHRENIA BULLETIN, 2009, 35 (05) : 851 - 854
  • [3] BREAKPOINT ANALYSIS OF NRXN1 DELETIONS IN SCHIZOPHRENIA
    Hoeffding, Louise K. E.
    Ingason, Andres
    Hansen, Thomas
    Werge, Thomas
    Rujescu, Dan
    SCHIZOPHRENIA RESEARCH, 2010, 117 (2-3) : 336 - 336
  • [4] Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
    Kanako Ishizuka
    Tomoyuki Yoshida
    Takeshi Kawabata
    Ayako Imai
    Hisashi Mori
    Hiroki Kimura
    Toshiya Inada
    Yuko Okahisa
    Jun Egawa
    Masahide Usami
    Itaru Kushima
    Mako Morikawa
    Takashi Okada
    Masashi Ikeda
    Aleksic Branko
    Daisuke Mori
    Toshiyuki Someya
    Nakao Iwata
    Norio Ozaki
    Journal of Neurodevelopmental Disorders, 2020, 12
  • [5] Incomplete penetrance of NRXN1 deletions in families with schizophrenia
    Todarello, Giovanna
    Feng, Ningping
    Kolachana, Bhaskar S.
    Li, Chao
    Vakkalanka, Radhakrishna
    Bertolino, Alessandro
    Weinberger, Daniel R.
    Straub, Richard E.
    SCHIZOPHRENIA RESEARCH, 2014, 155 (1-3) : 1 - 7
  • [6] NRXN1 Deletions in Schizophrenia Patients and Their Family Members But Not in Normal Controls
    Todarello, Giovanna
    Feng, Ningping
    Li, Chao
    Weinberger, Daniel R.
    Straub, Richard E.
    BIOLOGICAL PSYCHIATRY, 2011, 69 (09) : 250S - 250S
  • [7] Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
    Ishizuka, Kanako
    Yoshida, Tomoyuki
    Kawabata, Takeshi
    Imai, Ayako
    Mori, Hisashi
    Kimura, Hiroki
    Inada, Toshiya
    Okahisa, Yuko
    Egawa, Jun
    Usami, Masahide
    Kushima, Itaru
    Morikawa, Mako
    Okada, Takashi
    Ikeda, Masashi
    Branko, Aleksic
    Mori, Daisuke
    Someya, Toshiyuki
    Iwata, Nakao
    Ozaki, Norio
    JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2020, 12 (01)
  • [8] Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients
    Muehleisen, Thomas W.
    Basmanav, F. Buket
    Forstner, Andreas J.
    Mattheisen, Manuel
    Priebe, Lutz
    Herms, Stefan
    Breuer, Rene
    Moebus, Susanne
    Nenadic, Igor
    Sauer, Heinrich
    Moessner, Rainald
    Maier, Wolfgang
    Rujescu, Dan
    Ludwig, Michael
    Rietschel, Marcella
    Noethen, Markus M.
    Cichon, Sven
    SCHIZOPHRENIA RESEARCH, 2011, 127 (1-3) : 35 - 40
  • [9] Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
    Gauthier, Julie
    Siddiqui, Tabrez J.
    Huashan, Peng
    Yokomaku, Daisaku
    Hamdan, Fadi F.
    Champagne, Nathalie
    Lapointe, Mathieu
    Spiegelman, Dan
    Noreau, Anne
    Lafreniere, Ronald G.
    Fathalli, Ferid
    Joober, Ridha
    Krebs, Marie-Odile
    DeLisi, Lynn E.
    Mottron, Laurent
    Fombonne, Eric
    Michaud, Jacques L.
    Drapeau, Pierre
    Carbonetto, Salvatore
    Craig, Ann Marie
    Rouleau, Guy A.
    HUMAN GENETICS, 2011, 130 (04) : 563 - 573
  • [10] Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
    Julie Gauthier
    Tabrez J. Siddiqui
    Peng Huashan
    Daisaku Yokomaku
    Fadi F. Hamdan
    Nathalie Champagne
    Mathieu Lapointe
    Dan Spiegelman
    Anne Noreau
    Ronald G. Lafrenière
    Ferid Fathalli
    Ridha Joober
    Marie-Odile Krebs
    Lynn E. DeLisi
    Laurent Mottron
    Éric Fombonne
    Jacques L. Michaud
    Pierre Drapeau
    Salvatore Carbonetto
    Ann Marie Craig
    Guy A. Rouleau
    Human Genetics, 2011, 130 : 563 - 573