A citation-based method for searching scientific literature

Maryam Al Shehhi, Eva B Forman, Jacqueline E Fitzgerald, Veronica McInerney, Janusz Krawczyk, Sanbing Shen, David R Betts, Linda Mc Ardle, Kathleen M Gorman, Mary D King, Andrew Green, Louise Gallagher, Sally A Lynch. Eur J Med Genet 2019
Times Cited: 25







List of co-cited articles
161 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Investigation of NRXN1 deletions: clinical and molecular characterization.
Mindy Preston Dabell, Jill A Rosenfeld, Patricia Bader, Luis F Escobar, Dima El-Khechen, Stephanie E Vallee, Mary Beth Palko Dinulos, Cynthia Curry, Jamie Fisher, Raymond Tervo,[...]. Am J Med Genet A 2013
70
28

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
525
28

Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments.
Mark R Etherton, Cory A Blaiss, Craig M Powell, Thomas C Südhof. Proc Natl Acad Sci U S A 2009
281
24

A common cognitive, psychiatric, and dysmorphic phenotype in carriers of NRXN1 deletion.
Marina Viñas-Jornet, Susanna Esteba-Castillo, Elisabeth Gabau, Núria Ribas-Vidal, Neus Baena, Joan San, Anna Ruiz, Maria Dolors Coll, Ramon Novell, Miriam Guitart. Mol Genet Genomic Med 2014
24
25

Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature.
Frédérique Béna, Damien L Bruno, Mats Eriksson, Conny van Ravenswaaij-Arts, Zornitza Stark, Trijnie Dijkhuizen, Erica Gerkes, Stefania Gimelli, Devika Ganesamoorthy, Ann Charlotte Thuresson,[...]. Am J Med Genet B Neuropsychiatr Genet 2013
69
24

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
405
24

Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.
Christian P Schaaf, Philip M Boone, Srirangan Sampath, Charles Williams, Patricia I Bader, Jennifer M Mueller, Oleg A Shchelochkov, Chester W Brown, Heather P Crawford, James A Phalen,[...]. Eur J Hum Genet 2012
71
20

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.
Chelsea Lowther, Marsha Speevak, Christine M Armour, Elaine S Goh, Gail E Graham, Chumei Li, Susan Zeesman, Malgorzata J M Nowaczyk, Lee-Anne Schultz, Antonella Morra,[...]. Genet Med 2017
38
20

Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.
Hannah Mary Grayton, Markus Missler, David Andrew Collier, Cathy Fernandes. PLoS One 2013
93
20

Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1.
ChangHui Pak, Tamas Danko, Yingsha Zhang, Jason Aoto, Garret Anderson, Stephan Maxeiner, Fei Yi, Marius Wernig, Thomas C Südhof. Cell Stem Cell 2015
117
20

β-Neurexins Control Neural Circuits by Regulating Synaptic Endocannabinoid Signaling.
Garret R Anderson, Jason Aoto, Katsuhiko Tabuchi, Csaba Földy, Jason Covy, Ada Xin Yee, Dick Wu, Sung-Jin Lee, Lu Chen, Robert C Malenka,[...]. Cell 2015
71
20

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis.
Markus Missler, Weiqi Zhang, Astrid Rohlmann, Gunnar Kattenstroth, Robert E Hammer, Kurt Gottmann, Thomas C Südhof. Nature 2003
445
16

Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing.
Barbara Treutlein, Ozgun Gokce, Stephen R Quake, Thomas C Südhof. Proc Natl Acad Sci U S A 2014
155
16

Disruption of the neurexin 1 gene is associated with schizophrenia.
Dan Rujescu, Andres Ingason, Sven Cichon, Olli P H Pietiläinen, Michael R Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon,[...]. Hum Mol Genet 2009
336
16

Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders.
Linh Duong, Laura L Klitten, Rikke S Møller, Andrés Ingason, Klaus D Jakobsen, Celina Skjødt, Michael Didriksen, Helle Hjalgrim, Thomas Werge, Niels Tommerup. Am J Med Genet B Neuropsychiatr Genet 2012
50
16

CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.
Christiane Zweier, Eiko K de Jong, Markus Zweier, Alfredo Orrico, Lilian B Ousager, Amanda L Collins, Emilia K Bijlsma, Merel A W Oortveld, Arif B Ekici, André Reis,[...]. Am J Hum Genet 2009
230
16

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
Michael S L Ching, Yiping Shen, Wen-Hann Tan, Shafali S Jeste, Eric M Morrow, Xiaoli Chen, Nahit M Mukaddes, Seung-Yun Yoo, Ellen Hanson, Rachel Hundley,[...]. Am J Med Genet B Neuropsychiatr Genet 2010
195
16

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,[...]. Hum Genet 2011
171
16


A genome-wide investigation of SNPs and CNVs in schizophrenia.
Anna C Need, Dongliang Ge, Michael E Weale, Jessica Maia, Sheng Feng, Erin L Heinzen, Kevin V Shianna, Woohyun Yoon, Dalia Kasperaviciūte, Massimo Gennarelli,[...]. PLoS Genet 2009
354
16

Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters.
Victoria Harrison, Lyndsey Connell, Jesse Hayesmoore, Joanna McParland, Michael G Pike, Edward Blair. Am J Med Genet A 2011
54
16

Incomplete penetrance of NRXN1 deletions in families with schizophrenia.
Giovanna Todarello, Ningping Feng, Bhaskar S Kolachana, Chao Li, Radhakrishna Vakkalanka, Alessandro Bertolino, Daniel R Weinberger, Richard E Straub. Schizophr Res 2014
30
16

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
16

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
16

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
16



Copy number variations in neurodevelopmental disorders.
Hannah M Grayton, Cathy Fernandes, Dan Rujescu, David A Collier. Prog Neurobiol 2012
106
16

Conditional Deletion of All Neurexins Defines Diversity of Essential Synaptic Organizer Functions for Neurexins.
Lulu Y Chen, Man Jiang, Bo Zhang, Ozgun Gokce, Thomas C Südhof. Neuron 2017
80
16

Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality.
Matti Lam, Mohsen Moslem, Julien Bryois, Robin J Pronk, Elias Uhlin, Ivar Dehnisch Ellström, Loora Laan, Jessica Olive, Rebecca Morse, Harriet Rönnholm,[...]. Exp Cell Res 2019
20
20

Genome-wide association study of multiplex schizophrenia pedigrees.
Douglas F Levinson, Jianxin Shi, Kai Wang, Sang Oh, Brien Riley, Ann E Pulver, Dieter B Wildenauer, Claudine Laurent, Bryan J Mowry, Pablo V Gejman,[...]. Am J Psychiatry 2012
44
12

Analysis of the human neurexin genes: alternative splicing and the generation of protein diversity.
Lee Rowen, Janet Young, Brian Birditt, Amardeep Kaur, Anup Madan, Dana L Philipps, Shizhen Qin, Patrick Minx, Richard K Wilson, Leroy Hood,[...]. Genomics 2002
133
12

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.
Alden Y Huang, Dongmei Yu, Lea K Davis, Jae Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen,[...]. Neuron 2017
72
12

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.
Zhiqiang Li, Jianhua Chen, Yifeng Xu, Qizhong Yi, Weidong Ji, Peng Wang, Jiawei Shen, Zhijian Song, Meng Wang, Ping Yang,[...]. Biol Psychiatry 2016
36
12

Copy number variation in schizophrenia in the Japanese population.
Masashi Ikeda, Branko Aleksic, George Kirov, Yoko Kinoshita, Yoshio Yamanouchi, Tsuyoshi Kitajima, Kunihiro Kawashima, Tomo Okochi, Taro Kishi, Irina Zaharieva,[...]. Biol Psychiatry 2010
89
12

Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia.
James Dachtler, Jose L Ivorra, Tessa E Rowland, Colin Lever, R John Rodgers, Steven J Clapcote. Behav Neurosci 2015
39
12

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
George Kirov, Dilihan Gumus, Wei Chen, Nadine Norton, Lyudmila Georgieva, Murat Sari, Michael C O'Donovan, Fikret Erdogan, Michael J Owen, Hans-Hilger Ropers,[...]. Hum Mol Genet 2008
289
12

Neurexins.
Carsten Reissner, Fabian Runkel, Markus Missler. Genome Biol 2013
101
12

Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy.
Rikke S Møller, Yvonne G Weber, Laura L Klitten, Holger Trucks, Hiltrud Muhle, Wolfram S Kunz, Heather C Mefford, Andre Franke, Monika Kautza, Peter Wolf,[...]. Epilepsia 2013
46
12

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Tom Walsh, Jon M McClellan, Shane E McCarthy, Anjené M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari,[...]. Science 2008
12

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
12

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Peter Szatmari, Andrew D Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiao-Qing Liu, John B Vincent, Jennifer L Skaug, Ann P Thompson, Lili Senman,[...]. Nat Genet 2007
949
12

A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha.
F R Zahir, A Baross, A D Delaney, P Eydoux, N D Fernandes, T Pugh, M A Marra, J M Friedman. J Med Genet 2008
95
12

Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay.
Barbara Wiśniowiecka-Kowalnik, Monika Nesteruk, Sarika U Peters, Zhilian Xia, M Lance Cooper, Sarah Savage, R Stephen Amato, Patricia Bader, Marsha F Browning, Christa L Haun,[...]. Am J Med Genet B Neuropsychiatr Genet 2010
55
12

Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression.
Anne M Rochtus, Sara Trowbridge, Richard D Goldstein, Beth Rosen Sheidley, Sanjay P Prabhu, Robin Haynes, Hannah C Kinney, Annapurna H Poduri. Cold Spring Harb Mol Case Stud 2019
6
50

New copy number variations in schizophrenia.
Chiara Magri, Emilio Sacchetti, Michele Traversa, Paolo Valsecchi, Rita Gardella, Cristian Bonvicini, Alessandra Minelli, Massimo Gennarelli, Sergio Barlati. PLoS One 2010
69
12


Recurrent CNVs disrupt three candidate genes in schizophrenia patients.
Terry Vrijenhoek, Jacobine E Buizer-Voskamp, Inge van der Stelt, Eric Strengman, Chiara Sabatti, Ad Geurts van Kessel, Han G Brunner, Roel A Ophoff, Joris A Veltman. Am J Hum Genet 2008
204
12

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.
Anne Gregor, Beate Albrecht, Ingrid Bader, Emilia K Bijlsma, Arif B Ekici, Hartmut Engels, Karl Hackmann, Denise Horn, Juliane Hoyer, Jakub Klapecki,[...]. BMC Med Genet 2011
84
12



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.