A citation-based method for searching scientific literature

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, Lauren M McGrath, Cornelia Illmann, Paul Sandor, Cathy L Barr, Marco Grados, Harvey S Singer, Markus M Nöthen, Johannes Hebebrand, Robert A King, Yves Dion, Guy Rouleau, Cathy L Budman, Christel Depienne, Yulia Worbe, Andreas Hartmann, Kirsten R Müller-Vahl, Manfred Stuhrmann, Harald Aschauer, Mara Stamenkovic, Monika Schloegelhofer, Anastasios Konstantinidis, Gholson J Lyon, William M McMahon, Csaba Barta, Zsanett Tarnok, Peter Nagy, James R Batterson, Renata Rizzo, Danielle C Cath, Tomasz Wolanczyk, Cheston Berlin, Irene A Malaty, Michael S Okun, Douglas W Woods, Elliott Rees, Carlos N Pato, Michele T Pato, James A Knowles, Danielle Posthuma, David L Pauls, Nancy J Cox, Benjamin M Neale, Nelson B Freimer, Peristera Paschou, Carol A Mathews, Jeremiah M Scharf, Giovanni Coppola. Neuron 2017
Times Cited: 68







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



Times Cited
  Times     Co-cited
Similarity


De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
A Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, Robert A King, Andrea Dietrich, Jinchuan Xing, Stephan J Sanders, Jeffrey D Mandell, Alden Y Huang, Petra Richer,[...]. Neuron 2017
64
28

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
386
23

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
584
19

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
19

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
Lauren M McGrath, Dongmei Yu, Christian Marshall, Lea K Davis, Bhooma Thiruvahindrapuram, Bingbin Li, Carolina Cappi, Gloria Gerber, Aaron Wolf, Frederick A Schroeder,[...]. J Am Acad Child Adolesc Psychiatry 2014
68
17


Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
217
17

Familial Risks of Tourette Syndrome and Chronic Tic Disorders. A Population-Based Cohort Study.
David Mataix-Cols, Kayoko Isomura, Ana Pérez-Vigil, Zheng Chang, Christian Rück, K Johan Larsson, James F Leckman, Eva Serlachius, Henrik Larsson, Paul Lichtenstein. JAMA Psychiatry 2015
57
19


Gilles de la Tourette syndrome.
Mary M Robertson, Valsamma Eapen, Harvey S Singer, Davide Martino, Jeremiah M Scharf, Peristera Paschou, Veit Roessner, Douglas W Woods, Marwan Hariz, Carol A Mathews,[...]. Nat Rev Dis Primers 2017
99
14

Tourette syndrome is associated with recurrent exonic copy number variants.
Senthil K Sundaram, Ahm M Huq, Benjamin J Wilson, Harry T Chugani. Neurology 2010
81
14

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
14

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
14

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
14

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
O Mercati, G Huguet, A Danckaert, G André-Leroux, A Maruani, M Bellinzoni, T Rolland, L Gouder, A Mathieu, J Buratti,[...]. Mol Psychiatry 2017
32
28

CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.
Abhishek Nag, Elena G Bochukova, Barbara Kremeyer, Desmond D Campbell, Heike Muller, Ana V Valencia-Duarte, Julio Cardona, Isabel C Rivas, Sandra C Mesa, Mauricio Cuartas,[...]. PLoS One 2013
46
19

Genome-wide association study of Tourette's syndrome.
J M Scharf, D Yu, C A Mathews, B M Neale, S E Stewart, J A Fagerness, P Evans, E Gamazon, C K Edlund, S K Service,[...]. Mol Psychiatry 2013
102
13

An international perspective on Tourette syndrome: selected findings from 3,500 individuals in 22 countries.
R D Freeman, D K Fast, L Burd, J Kerbeshian, M M Robertson, P Sandor. Dev Med Child Neurol 2000
475
13

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
68
13

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
276
13

Decreased number of parvalbumin and cholinergic interneurons in the striatum of individuals with Tourette syndrome.
Yuko Kataoka, Paul S A Kalanithi, Heidi Grantz, Michael L Schwartz, Clifford Saper, James F Leckman, Flora M Vaccarino. J Comp Neurol 2010
260
11

Familial clustering of tic disorders and obsessive-compulsive disorder.
Heidi A Browne, Stefan N Hansen, Joseph D Buxbaum, Shannon L Gair, Judith B Nissen, Kathrine H Nikolajsen, Diana E Schendel, Abraham Reichenberg, Erik T Parner, Dorothy E Grice. JAMA Psychiatry 2015
31
25

Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome.
Matthew E Hirschtritt, Paul C Lee, David L Pauls, Yves Dion, Marco A Grados, Cornelia Illmann, Robert A King, Paul Sandor, William M McMahon, Gholson J Lyon,[...]. JAMA Psychiatry 2015
217
11

Prevalence of tic disorders: a systematic review and meta-analysis.
Tristan Knight, Thomas Steeves, Lundy Day, Mark Lowerison, Nathalie Jette, Tamara Pringsheim. Pediatr Neurol 2012
182
11

De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
937
11

A twin study of Tourette syndrome.
R A Price, K K Kidd, D J Cohen, D L Pauls, J F Leckman. Arch Gen Psychiatry 1985
234
11

Population prevalence of Tourette syndrome: a systematic review and meta-analysis.
Jeremiah M Scharf, Laura L Miller, Caitlin A Gauvin, Janelle Alabiso, Carol A Mathews, Yoav Ben-Shlomo. Mov Disord 2015
107
11

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
75
11

Presynaptic neurexin-3 alternative splicing trans-synaptically controls postsynaptic AMPA receptor trafficking.
Jason Aoto, David C Martinelli, Robert C Malenka, Katsuhiko Tabuchi, Thomas C Südhof. Cell 2013
168
11

CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders.
Jie Hu, Jun Liao, Malini Sathanoori, Sally Kochmar, Jessica Sebastian, Svetlana A Yatsenko, Urvashi Surti. J Neurodev Disord 2015
43
16

Altered parvalbumin-positive neuron distribution in basal ganglia of individuals with Tourette syndrome.
Paul S A Kalanithi, Wei Zheng, Yuko Kataoka, Marian DiFiglia, Heidi Grantz, Clifford B Saper, Michael L Schwartz, James F Leckman, Flora M Vaccarino. Proc Natl Acad Sci U S A 2005
320
10

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
Lea K Davis, Dongmei Yu, Clare L Keenan, Eric R Gamazon, Anuar I Konkashbaev, Eske M Derks, Benjamin M Neale, Jian Yang, S Hong Lee, Patrick Evans,[...]. PLoS Genet 2013
142
10

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
Thomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, A Gulhan Ercan-Sencicek, Young-Shin Kim, Daniel O Fishman, Melanie J Raubeson, Youeun Song, Katsuhito Yasuno, Winson S C Ho,[...]. Biol Psychiatry 2012
114
10

The Inheritance of Tourette Disorder: A review.
David L Pauls, Thomas V Fernandez, Carol A Mathews, Matthew W State, Jeremiah M Scharf. J Obsessive Compuls Relat Disord 2014
39
17

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.
Marianthi Georgitsi, A Jeremy Willsey, Carol A Mathews, Matthew State, Jeremiah M Scharf, Peristera Paschou. Front Neurosci 2016
23
30

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
151
10


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
113
10

A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders.
Asami Oguro-Ando, Amila Zuko, Kristel T E Kleijer, J Peter H Burbach. Mol Cell Neurosci 2017
39
15

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
35
17

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.
Annemieke J M H Verkerk, Carol A Mathews, Marijke Joosse, Bert H J Eussen, Peter Heutink, Ben A Oostra. Genomics 2003
163
8

L-histidine decarboxylase and Tourette's syndrome.
A Gulhan Ercan-Sencicek, Althea A Stillman, Ananda K Ghosh, Kaya Bilguvar, Brian J O'Roak, Christopher E Mason, Thomas Abbott, Abha Gupta, Robert A King, David L Pauls,[...]. N Engl J Med 2010
193
8


Gilles de la Tourette syndrome is associated with hypermethylation of the dopamine D2 receptor gene.
Kirsten R Müller-Vahl, Gesa Loeber, Alexandra Kotsiari, Linda Müller-Engling, Helge Frieling. J Psychiatr Res 2017
16
37

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.
Dongmei Yu, Carol A Mathews, Jeremiah M Scharf, Benjamin M Neale, Lea K Davis, Eric R Gamazon, Eske M Derks, Patrick Evans, Christopher K Edlund, Jacquelyn Crane,[...]. Am J Psychiatry 2015
74
8

Transcriptome Analysis of the Human Striatum in Tourette Syndrome.
Jessica B Lennington, Gianfilippo Coppola, Yuko Kataoka-Sasaki, Thomas V Fernandez, Dean Palejev, Yifan Li, Anita Huttner, Mihovil Pletikos, Nenad Sestan, James F Leckman,[...]. Biol Psychiatry 2016
86
8

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
793
8


Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Tarjinder Singh, Mitja I Kurki, David Curtis, Shaun M Purcell, Lucy Crooks, Jeremy McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen,[...]. Nat Neurosci 2016
205
8

Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins.
Ethan R Graf, XueZhao Zhang, Shan-Xue Jin, Michael W Linhoff, Ann Marie Craig. Cell 2004
654
8


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.