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Neuronal impact of patient-specific aberrant NRXN1α splicing
Author / Creator:Flaherty, Erin ; Zhu, Shijia ; Barretto, Natalie ; Cheng, Esther ; Deans, P. J. Michael ; Fernando, Michael B. ; Schrode, Nadine ; Francoeur, Nancy ; Antoine, Alesia ; Alganem, Khaled ; Halpern, Madeline ; Deikus, Gintaras ; Shah, Hardik ; Fitzgerald, Megan ; Ladran, Ian ; Gochman, Peter ; Rapoport, Judith ; Tsankova, Nadejda M. ; McCullumsmith, Robert ; Hoffman, Gabriel E. ; Sebra, Robert ; Fang, Gang ; Brennand, Kristen J.
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2019-12, Vol.51 (12), p.1679-1690
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NRXN1α +/- is associated with increased excitability in ASD iPSC-derived neurons
Author / Creator:Avazzadeh, Sahar ; Quinlan, Leo R ; Reilly, Jamie ; McDonagh, Katya ; Jalali, Amirhossein ; Wang, Yanqin ; McInerney, Veronica ; Krawczyk, Janusz ; Ding, Yicheng ; Fitzgerald, Jacqueline ; O'Sullivan, Matthew ; Forman, Eva B ; Lynch, Sally A ; Ennis, Sean ; Feerick, Niamh ; Reilly, Richard ; Li, Weidong ; Shen, Xu ; Yang, Guangming ; Lu, Yin ; Peeters, Hilde ; Dockery, Peter ; O'Brien, Timothy ; Shen, Sanbing ; Gallagher, Louise
Publisher:England: BioMed Central
Journal title:BMC neuroscience, 2021-09, Vol.22 (1), p.56-56, Article 56
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Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders
Author / Creator:Hu, Zhonghua ; Xiao, Xiao ; Zhang, Zhuohua ; Li, Ming
Publisher:London: Nature Publishing Group UK
Journal title:Molecular psychiatry, 2019-10, Vol.24 (10), p.1400-1414
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Phenotypic spectrum and genotype―phenotype correlations of NRXN1 exon deletions
Author / Creator:SCHAAF, Christian P ; BOONE, Philip M ; TARTAGLIA, Nicole R ; EVANS, Patricia ; CAMPBELL, William M ; TSAI, Anne Chun-Hui ; PARSLEY, Lea ; GRAYSON, Stephanie W ; SCHEUERLE, Angela ; LUZZI, Carol D ; THOMAS, Sandra K ; ENG, Patricia A ; SAMPATH, Srirangan ; KANG, Sung-Hae L ; PATEL, Ankita ; STANKIEWICZ, Pawel ; CHEUNG, Sau W ; WILLIAMS, Charles ; BADER, Patricia I ; MUELLER, Jennifer M ; SHCHELOCHKOV, Oleg A ; BROWN, Chester W ; CRAWFORD, Heather P ; PHALEN, James A
Publisher:Basingstoke: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2012-12, Vol.20 (12), p.1240-1247
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The clinical relevance of intragenic NRXN1 deletions
Author / Creator:Cosemans, Nele ; Vandenhove, Laura ; Vogels, Annick ; Devriendt, Koenraad ; Van Esch, Hilde ; Van Buggenhout, Griet ; Olivié, Hilde ; de Ravel, Thomy ; Ortibus, Els ; Legius, Eric ; Aerssens, Peter ; Breckpot, Jeroen ; R. Vermeesch, Joris ; Shen, Sanbing ; Fitzgerald, Jacqueline ; Gallagher, Louise ; Peeters, Hilde
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2020-05, Vol.57 (5), p.347-355
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Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids
Author / Creator:Sebastian, Rebecca ; Jin, Kang ; Pavon, Narciso ; Bansal, Ruby ; Potter, Andrew ; Song, Yoonjae ; Babu, Juliana ; Gabriel, Rafael ; Sun, Yubing ; Aronow, Bruce ; Pak, ChangHui
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2023-06, Vol.14 (1), p.3770-3770, Article 3770
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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
Author / Creator:Gauthier, Julie ; Siddiqui, Tabrez J. ; Huashan, Peng ; Yokomaku, Daisaku ; Hamdan, Fadi F. ; Champagne, Nathalie ; Lapointe, Mathieu ; Spiegelman, Dan ; Noreau, Anne ; Lafrenière, Ronald G. ; Fathalli, Ferid ; Joober, Ridha ; Krebs, Marie-Odile ; DeLisi, Lynn E. ; Mottron, Laurent ; Fombonne, Éric ; Michaud, Jacques L. ; Drapeau, Pierre ; Carbonetto, Salvatore ; Craig, Ann Marie ; Rouleau, Guy A.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Human genetics, 2011-10, Vol.130 (4), p.563-573
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Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice
Author / Creator:Xu, Bing ; Ho, Yugong ; Fasolino, Maria ; Medina, Joanna ; O'Brien, William Timothy ; Lamonica, Janine M ; Nugent, Erin ; Brodkin, Edward S ; Fuccillo, Marc V ; Bucan, Maja ; Zhou, Zhaolan
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2023-02, Vol.19 (2), p.e1010659-e1010659
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Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
Author / Creator:Pak, ChangHui ; Danko, Tamas ; Mirabella, Vincent R. ; Wang, Jinzhao ; Liu, Yingfei ; Vangipuram, Madhuri ; Grieder, Sarah ; Zhang, Xianglong ; Ward, Thomas ; Huang, Yu-Wen Alvin ; Jin, Kang ; Dexheimer, Philip ; Bardes, Eric ; Mitelpunkt, Alexis ; Ma, Junyi ; McLachlan, Michael ; Moore, Jennifer C. ; Qu, Pingping ; Purmann, Carolin ; Dage, Jeffrey L. ; Swanson, Bradley J. ; Urban, Alexander E. ; Aronow, Bruce J. ; Pang, Zhiping P. ; Levinson, Douglas F. ; Wernig, Marius ; Südhof, Thomas C.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2021-06, Vol.118 (22), p.1-12
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Disruption of Nrxn1α within excitatory forebrain circuits drives value-based dysfunction
Author / Creator:Alabi, Opeyemi O ; Davatolhagh, M Felicia ; Robinson, Mara ; Fortunato, Michael P ; Vargas Cifuentes, Luigim ; Kable, Joseph W ; Fuccillo, Marc Vincent
Publisher:England: eLife Sciences Publications, Ltd
Journal title:eLife, 2020-12, Vol.9
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NRXN1 as a Prognostic Biomarker: Linking Copy Number Variation to EMT and Survival in Colon Cancer
Author / Creator:Bang, Hyun Jin ; Shim, Hyun-Jeong ; Park, Mi-Ra ; Yoon, Sumin ; Yoo, Kyung Hyun ; Kim, Young-Kook ; Lee, Hyunju ; Nam, Jeong-Seok ; Hwang, Jun-Eul ; Bae, Woo-Kyun ; Chung, Ik-Joo ; Sun, Eun-Gene ; Cho, Sang-Hee
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-11, Vol.25 (21), p.11423
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Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
Author / Creator:Lowther, Chelsea ; Speevak, Marsha ; Armour, Christine M. ; Goh, Elaine S. ; Graham, Gail E. ; Li, Chumei ; Zeesman, Susan ; Nowaczyk, Malgorzata J.M. ; Schultz, Lee-Anne ; Morra, Antonella ; Nicolson, Rob ; Bikangaga, Peter ; Samdup, Dawa ; Zaazou, Mostafa ; Boyd, Kerry ; Jung, Jack H. ; Siu, Victoria ; Rajguru, Manjulata ; Goobie, Sharan ; Tarnopolsky, Mark A. ; Prasad, Chitra ; Dick, Paul T. ; Hussain, Asmaa S. ; Walinga, Margreet ; Reijenga, Renske G. ; Gazzellone, Matthew ; Lionel, Anath C. ; Marshall, Christian R. ; Scherer, Stephen W. ; Stavropoulos, Dimitri J. ; McCready, Elizabeth ; Bassett, Anne S.
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2017-01, Vol.19 (1), p.53-61
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Allelic contribution of Nrxn1[alpha] to autism-relevant behavioral phenotypes in mice
Author / Creator:Xu, Bing ; Ho, Yugong ; Fasolino, Maria ; Medina, Joanna ; O'Brien, William Timothy ; Lamonica, Janine M ; Nugent, Erin ; Brodkin, Edward S ; Fuccillo, Marc V ; Bucan, Maja ; Zhou, Zhaolan
Publisher:Public Library of Science
Journal title:PLoS genetics, 2023-02, Vol.19 (2), p.e1010659
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Neuronal impact of patient-specific aberrant NRXN1[alpha] splicing
Author / Creator:Flaherty, Erin ; Zhu, Shijia ; Barretto, Natalie ; Cheng, Esther ; Deans, P. J. Michael ; Fernando, Michael B ; Schrode, Nadine
Publisher:Nature Publishing Group
Journal title:Nature genetics, 2019-12, Vol.51 (12), p.1679
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Deletion of NRXN1α impairs long-range and local connectivity in amygdala fear circuit
Author / Creator:Asede, Douglas ; Joseph, Asnel ; Bolton, McLean M.
Publisher:London: Nature Publishing Group UK
Journal title:Translational psychiatry, 2020-07, Vol.10 (1), p.242-242, Article 242
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CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1
Author / Creator:Nag, Abhishek ; Bochukova, Elena G ; Kremeyer, Barbara ; Campbell, Desmond D ; Muller, Heike ; Valencia-Duarte, Ana V ; Cardona, Julio ; Rivas, Isabel C ; Mesa, Sandra C ; Cuartas, Mauricio ; Garcia, Jharley ; Bedoya, Gabriel ; Cornejo, William ; Herrera, Luis D ; Romero, Roxana ; Fournier, Eduardo ; Reus, Victor I ; Lowe, Thomas L ; Farooqi, I Sadaf ; Mathews, Carol A ; McGrath, Lauren M ; Yu, Dongmei ; Cook, Ed ; Wang, Kai ; Scharf, Jeremiah M ; Pauls, David L ; Freimer, Nelson B ; Plagnol, Vincent ; Ruiz-Linares, Andrés
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-03, Vol.8 (3), p.e59061-e59061
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Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia
Author / Creator: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
Publisher:England: BioMed Central Ltd
Journal title:Journal of neurodevelopmental disorders, 2020-09, Vol.12 (1), p.25-25, Article 25
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Role of LncMALAT1-miR-141-3p/200a-3p-NRXN1 Axis in the Impairment of Learning and Memory Capacity in ADHD
Author / Creator:MU, Y ; LI, J ; ZHANG, S ; ZHONG, F ; ZHANG, X ; SONG, J ; YUAN, H ; TIAN, T ; HU, Y
Publisher:Praha: Institute of Physiology
Journal title:Physiological research, 2023-11, Vol.72 (5), p.645-656
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Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models
Author / Creator:Zeng, Liyun ; Zhang, Peilin ; Shi, Lingling ; Yamamoto, Vicky ; Lu, Wange ; Wang, Kai
Publisher:United States: Public Library of Science
Journal title:PloS one, 2013-03, Vol.8 (3), p.e59685-e59685
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Increased Ca2+ signaling in NRXN1α+/− neurons derived from ASD induced pluripotent stem cells
Author / Creator:Avazzadeh, Sahar ; McDonagh, Katya ; Reilly, Jamie ; Wang, Yanqin ; Boomkamp, Stephanie D. ; McInerney, Veronica ; Krawczyk, Janusz ; Fitzgerald, Jacqueline ; Feerick, Niamh ; O’Sullivan, Matthew ; Jalali, Amirhossein ; Forman, Eva B. ; Lynch, Sally A. ; Ennis, Sean ; Cosemans, Nele ; Peeters, Hilde ; Dockery, Peter ; O’Brien, Timothy ; Quinlan, Leo R. ; Gallagher, Louise ; Shen, Sanbing
Publisher:London: BioMed Central
Journal title:Molecular autism, 2019-12, Vol.10 (1), p.1-52, Article 52
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Neuronal impact of patient-specific aberrant NRXN1α splicing

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NRXN1α +/- is associated with increased excitability in ASD iPSC-derived neurons

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Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders

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Phenotypic spectrum and genotype―phenotype correlations of NRXN1 exon deletions

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The clinical relevance of intragenic NRXN1 deletions

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Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids

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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

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Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice

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Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons

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Disruption of Nrxn1α within excitatory forebrain circuits drives value-based dysfunction

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NRXN1 as a Prognostic Biomarker: Linking Copy Number Variation to EMT and Survival in Colon Cancer

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Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression

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Allelic contribution of Nrxn1[alpha] to autism-relevant behavioral phenotypes in mice

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Neuronal impact of patient-specific aberrant NRXN1[alpha] splicing

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Deletion of NRXN1α impairs long-range and local connectivity in amygdala fear circuit

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CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1

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Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia

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Role of LncMALAT1-miR-141-3p/200a-3p-NRXN1 Axis in the Impairment of Learning and Memory Capacity in ADHD

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Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell models

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Increased Ca2+ signaling in NRXN1α+/− neurons derived from ASD induced pluripotent stem cells

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