Benjamin Rein, Zhen Yan. Trends Neurosci 2020
Times Cited: 16
Times Cited: 16
Times Cited
Times Co-cited
Similarity
Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
25
16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
25
Chemogenetic Activation of Prefrontal Cortex Rescues Synaptic and Behavioral Deficits in a Mouse Model of 16p11.2 Deletion Syndrome.
Wei Wang, Benjamin Rein, Freddy Zhang, Tao Tan, Ping Zhong, Luye Qin, Zhen Yan. J Neurosci 2018
Wei Wang, Benjamin Rein, Freddy Zhang, Tao Tan, Ping Zhong, Luye Qin, Zhen Yan. J Neurosci 2018
18
Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Guy Horev, Jacob Ellegood, Jason P Lerch, Young-Eun E Son, Lakshmi Muthuswamy, Hannes Vogel, Abba M Krieger, Andreas Buja, R Mark Henkelman, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2011
Guy Horev, Jacob Ellegood, Jason P Lerch, Young-Eun E Son, Lakshmi Muthuswamy, Hannes Vogel, Abba M Krieger, Andreas Buja, R Mark Henkelman, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2011
18
12
Opposing brain differences in 16p11.2 deletion and duplication carriers.
Abid Y Qureshi, Sophia Mueller, Abraham Z Snyder, Pratik Mukherjee, Jeffrey I Berman, Timothy P L Roberts, Srikantan S Nagarajan, John E Spiro, Wendy K Chung, Elliott H Sherr,[...]. J Neurosci 2014
Abid Y Qureshi, Sophia Mueller, Abraham Z Snyder, Pratik Mukherjee, Jeffrey I Berman, Timothy P L Roberts, Srikantan S Nagarajan, John E Spiro, Wendy K Chung, Elliott H Sherr,[...]. J Neurosci 2014
12
Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2016.
Matthew J Maenner, Kelly A Shaw, Jon Baio, Anita Washington, Mary Patrick, Monica DiRienzo, Deborah L Christensen, Lisa D Wiggins, Sydney Pettygrove, Jennifer G Andrews,[...]. MMWR Surveill Summ 2020
Matthew J Maenner, Kelly A Shaw, Jon Baio, Anita Washington, Mary Patrick, Monica DiRienzo, Deborah L Christensen, Lisa D Wiggins, Sydney Pettygrove, Jennifer G Andrews,[...]. MMWR Surveill Summ 2020
12
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
12
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
Bradley P Coe, Holly A F Stessman, Arvis Sulovari, Madeleine R Geisheker, Trygve E Bakken, Allison M Lake, Joseph D Dougherty, Ed S Lein, Fereydoun Hormozdiari, Raphael A Bernier,[...]. Nat Genet 2019
Bradley P Coe, Holly A F Stessman, Arvis Sulovari, Madeleine R Geisheker, Trygve E Bakken, Allison M Lake, Joseph D Dougherty, Ed S Lein, Fereydoun Hormozdiari, Raphael A Bernier,[...]. Nat Genet 2019
12
Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
12
Stress Exposure in Dopamine D4 Receptor Knockout Mice Induces Schizophrenia-Like Behaviors via Disruption of GABAergic Transmission.
Tao Tan, Wei Wang, Jamal Williams, Kaijie Ma, Qing Cao, Zhen Yan. Schizophr Bull 2019
Tao Tan, Wei Wang, Jamal Williams, Kaijie Ma, Qing Cao, Zhen Yan. Schizophr Bull 2019
20
Histone deacetylase inhibitor MS-275 restores social and synaptic function in a Shank3-deficient mouse model of autism.
Kaijie Ma, Luye Qin, Emmanuel Matas, Lara J Duffney, Aiyi Liu, Zhen Yan. Neuropsychopharmacology 2018
Kaijie Ma, Luye Qin, Emmanuel Matas, Lara J Duffney, Aiyi Liu, Zhen Yan. Neuropsychopharmacology 2018
12
The activity-dependent transcription factor NPAS4 regulates domain-specific inhibition.
Brenda L Bloodgood, Nikhil Sharma, Heidi Adlman Browne, Alissa Z Trepman, Michael E Greenberg. Nature 2013
Brenda L Bloodgood, Nikhil Sharma, Heidi Adlman Browne, Alissa Z Trepman, Michael E Greenberg. Nature 2013
12
Amelioration of autism-like social deficits by targeting histone methyltransferases EHMT1/2 in Shank3-deficient mice.
Zi-Jun Wang, Ping Zhong, Kaijie Ma, Ji-Seon Seo, Fengwei Yang, Zihua Hu, Freddy Zhang, Lin Lin, Jie Wang, Tao Liu,[...]. Mol Psychiatry 2020
Zi-Jun Wang, Ping Zhong, Kaijie Ma, Ji-Seon Seo, Fengwei Yang, Zihua Hu, Freddy Zhang, Lin Lin, Jie Wang, Tao Liu,[...]. Mol Psychiatry 2020
12
Social deficits in Shank3-deficient mouse models of autism are rescued by histone deacetylase (HDAC) inhibition.
Luye Qin, Kaijie Ma, Zi-Jun Wang, Zihua Hu, Emmanuel Matas, Jing Wei, Zhen Yan. Nat Neurosci 2018
Luye Qin, Kaijie Ma, Zi-Jun Wang, Zihua Hu, Emmanuel Matas, Jing Wei, Zhen Yan. Nat Neurosci 2018
12
Behavioral, circuitry, and molecular aberrations by region-specific deficiency of the high-risk autism gene Cul3.
Maximiliano Rapanelli, Tao Tan, Wei Wang, Xue Wang, Zi-Jun Wang, Ping Zhong, Luciana Frick, Luye Qin, Kaijie Ma, Jun Qu,[...]. Mol Psychiatry 2021
Maximiliano Rapanelli, Tao Tan, Wei Wang, Xue Wang, Zi-Jun Wang, Ping Zhong, Luciana Frick, Luye Qin, Kaijie Ma, Jun Qu,[...]. Mol Psychiatry 2021
12
Reversal of synaptic and behavioral deficits in a 16p11.2 duplication mouse model via restoration of the GABA synapse regulator Npas4.
Benjamin Rein, Tao Tan, Fengwei Yang, Wei Wang, Jamal Williams, Freddy Zhang, Alea Mills, Zhen Yan. Mol Psychiatry 2021
Benjamin Rein, Tao Tan, Fengwei Yang, Wei Wang, Jamal Williams, Freddy Zhang, Alea Mills, Zhen Yan. Mol Psychiatry 2021
20
Repeated stress causes cognitive impairment by suppressing glutamate receptor expression and function in prefrontal cortex.
Eunice Y Yuen, Jing Wei, Wenhua Liu, Ping Zhong, Xiangning Li, Zhen Yan. Neuron 2012
Eunice Y Yuen, Jing Wei, Wenhua Liu, Ping Zhong, Xiangning Li, Zhen Yan. Neuron 2012
12
Activity-dependent regulation of inhibitory synapse development by Npas4.
Yingxi Lin, Brenda L Bloodgood, Jessica L Hauser, Ariya D Lapan, Alex C Koon, Tae-Kyung Kim, Linda S Hu, Athar N Malik, Michael E Greenberg. Nature 2008
Yingxi Lin, Brenda L Bloodgood, Jessica L Hauser, Ariya D Lapan, Alex C Koon, Tae-Kyung Kim, Linda S Hu, Athar N Malik, Michael E Greenberg. Nature 2008
12
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
12
Prodromal and autistic symptoms in schizotypal personality disorder and 22q11.2 deletion syndrome.
Michelle L Esterberg, Opal Y Ousley, Joseph F Cubells, Elaine F Walker. J Abnorm Psychol 2013
Michelle L Esterberg, Opal Y Ousley, Joseph F Cubells, Elaine F Walker. J Abnorm Psychol 2013
20
Psychiatric disorders in children with 16p11.2 deletion and duplication.
Maria Niarchou, Samuel J R A Chawner, Joanne L Doherty, Anne M Maillard, Sébastien Jacquemont, Wendy K Chung, LeeAnne Green-Snyder, Raphael A Bernier, Robin P Goin-Kochel, Ellen Hanson,[...]. Transl Psychiatry 2019
Maria Niarchou, Samuel J R A Chawner, Joanne L Doherty, Anne M Maillard, Sébastien Jacquemont, Wendy K Chung, LeeAnne Green-Snyder, Raphael A Bernier, Robin P Goin-Kochel, Ellen Hanson,[...]. Transl Psychiatry 2019
12
The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
12
Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndrome.
Axel Weber, Angelika Köhler, Andreas Hahn, Bernd Neubauer, Ulrich Müller. Neurogenetics 2013
Axel Weber, Angelika Köhler, Andreas Hahn, Bernd Neubauer, Ulrich Müller. Neurogenetics 2013
12
Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
Russell C Dale, Padraic Grattan-Smith, Michelle Nicholson, Greg B Peters. Dev Med Child Neurol 2012
Russell C Dale, Padraic Grattan-Smith, Michelle Nicholson, Greg B Peters. Dev Med Child Neurol 2012
12
Clinical features of 78 adults with 22q11 Deletion Syndrome.
Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
12
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
12
Relationship between parent-reported gastrointestinal symptoms, sleep problems, autism spectrum disorder symptoms, and behavior problems in children and adolescents with 22q11.2 deletion syndrome.
Geraldine Leader, Maeve Murray, Páraic S O'Súilleabháin, Leanne Maher, Katie Naughton, Sophia Arndt, Keeley White, Ivan Traina, Arlene Mannion. Res Dev Disabil 2020
Geraldine Leader, Maeve Murray, Páraic S O'Súilleabháin, Leanne Maher, Katie Naughton, Sophia Arndt, Keeley White, Ivan Traina, Arlene Mannion. Res Dev Disabil 2020
40
Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
12
Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
12
Complex Oscillatory Waves Emerging from Cortical Organoids Model Early Human Brain Network Development.
Cleber A Trujillo, Richard Gao, Priscilla D Negraes, Jing Gu, Justin Buchanan, Sebastian Preissl, Allen Wang, Wei Wu, Gabriel G Haddad, Isaac A Chaim,[...]. Cell Stem Cell 2019
Cleber A Trujillo, Richard Gao, Priscilla D Negraes, Jing Gu, Justin Buchanan, Sebastian Preissl, Allen Wang, Wei Wu, Gabriel G Haddad, Isaac A Chaim,[...]. Cell Stem Cell 2019
6
The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.
Mary Kusenda, Vladimir Vacic, Dheeraj Malhotra, Linda Rodgers, Kevin Pavon, Jennifer Meth, Ravinesh A Kumar, Susan L Christian, Hilde Peeters, Shawn S Cho,[...]. J Child Neurol 2015
Mary Kusenda, Vladimir Vacic, Dheeraj Malhotra, Linda Rodgers, Kevin Pavon, Jennifer Meth, Ravinesh A Kumar, Susan L Christian, Hilde Peeters, Shawn S Cho,[...]. J Child Neurol 2015
20
Pharmacological Inhibition of ERK Signaling Rescues Pathophysiology and Behavioral Phenotype Associated with 16p11.2 Chromosomal Deletion in Mice.
Joanna Pucilowska, Joseph Vithayathil, Marco Pagani, Caitlin Kelly, J Colleen Karlo, Camilla Robol, Ilaria Morella, Alessandro Gozzi, Riccardo Brambilla, Gary E Landreth. J Neurosci 2018
Joanna Pucilowska, Joseph Vithayathil, Marco Pagani, Caitlin Kelly, J Colleen Karlo, Camilla Robol, Ilaria Morella, Alessandro Gozzi, Riccardo Brambilla, Gary E Landreth. J Neurosci 2018
6
Genome engineering using the CRISPR-Cas9 system.
F Ann Ran, Patrick D Hsu, Jason Wright, Vineeta Agarwala, David A Scott, Feng Zhang. Nat Protoc 2013
F Ann Ran, Patrick D Hsu, Jason Wright, Vineeta Agarwala, David A Scott, Feng Zhang. Nat Protoc 2013
6
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication.
Megan Y Dennis, Xander Nuttle, Peter H Sudmant, Francesca Antonacci, Tina A Graves, Mikhail Nefedov, Jill A Rosenfeld, Saba Sajjadian, Maika Malig, Holland Kotkiewicz,[...]. Cell 2012
Megan Y Dennis, Xander Nuttle, Peter H Sudmant, Francesca Antonacci, Tina A Graves, Mikhail Nefedov, Jill A Rosenfeld, Saba Sajjadian, Maika Malig, Holland Kotkiewicz,[...]. Cell 2012
6
Model mice for 15q11-13 duplication syndrome exhibit late-onset obesity and altered lipid metabolism.
Rui Kishimoto, Kota Tamada, Xiaoxi Liu, Hiroko Okubo, Satoko Ise, Hisashi Ohta, Sandra Ruf, Jin Nakatani, Nobuoki Kohno, François Spitz,[...]. Hum Mol Genet 2015
Rui Kishimoto, Kota Tamada, Xiaoxi Liu, Hiroko Okubo, Satoko Ise, Hisashi Ohta, Sandra Ruf, Jin Nakatani, Nobuoki Kohno, François Spitz,[...]. Hum Mol Genet 2015
9
STRING v11: protein-protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets.
Damian Szklarczyk, Annika L Gable, David Lyon, Alexander Junge, Stefan Wyder, Jaime Huerta-Cepas, Milan Simonovic, Nadezhda T Doncheva, John H Morris, Peer Bork,[...]. Nucleic Acids Res 2019
Damian Szklarczyk, Annika L Gable, David Lyon, Alexander Junge, Stefan Wyder, Jaime Huerta-Cepas, Milan Simonovic, Nadezhda T Doncheva, John H Morris, Peer Bork,[...]. Nucleic Acids Res 2019
6
Mutations causing syndromic autism define an axis of synaptic pathophysiology.
Benjamin D Auerbach, Emily K Osterweil, Mark F Bear. Nature 2011
Benjamin D Auerbach, Emily K Osterweil, Mark F Bear. Nature 2011
6
Metascape provides a biologist-oriented resource for the analysis of systems-level datasets.
Yingyao Zhou, Bin Zhou, Lars Pache, Max Chang, Alireza Hadj Khodabakhshi, Olga Tanaseichuk, Christopher Benner, Sumit K Chanda. Nat Commun 2019
Yingyao Zhou, Bin Zhou, Lars Pache, Max Chang, Alireza Hadj Khodabakhshi, Olga Tanaseichuk, Christopher Benner, Sumit K Chanda. Nat Commun 2019
6
16p11.2 microdeletion imparts transcriptional alterations in human iPSC-derived models of early neural development.
Julien G Roth, Kristin L Muench, Aditya Asokan, Victoria M Mallett, Hui Gai, Yogendra Verma, Stephen Weber, Carol Charlton, Jonas L Fowler, Kyle M Loh,[...]. Elife 2020
Julien G Roth, Kristin L Muench, Aditya Asokan, Victoria M Mallett, Hui Gai, Yogendra Verma, Stephen Weber, Carol Charlton, Jonas L Fowler, Kyle M Loh,[...]. Elife 2020
25
The pathophysiology of fragile X (and what it teaches us about synapses).
Asha L Bhakar, Gül Dölen, Mark F Bear. Annu Rev Neurosci 2012
Asha L Bhakar, Gül Dölen, Mark F Bear. Annu Rev Neurosci 2012
6
TrkB regulates hippocampal neurogenesis and governs sensitivity to antidepressive treatment.
Yun Li, Bryan W Luikart, Shari Birnbaum, Jian Chen, Chang-Hyuk Kwon, Steven G Kernie, Rhonda Bassel-Duby, Luis F Parada. Neuron 2008
Yun Li, Bryan W Luikart, Shari Birnbaum, Jian Chen, Chang-Hyuk Kwon, Steven G Kernie, Rhonda Bassel-Duby, Luis F Parada. Neuron 2008
6
Trk signaling regulates neural precursor cell proliferation and differentiation during cortical development.
Katarzyna Bartkowska, Annie Paquin, Andrée S Gauthier, David R Kaplan, Freda D Miller. Development 2007
Katarzyna Bartkowska, Annie Paquin, Andrée S Gauthier, David R Kaplan, Freda D Miller. Development 2007
6
GDNF and GFRalpha1 promote formation of neuronal synapses by ligand-induced cell adhesion.
Fernanda Ledda, Gustavo Paratcha, Tatiana Sandoval-Guzmán, Carlos F Ibáñez. Nat Neurosci 2007
Fernanda Ledda, Gustavo Paratcha, Tatiana Sandoval-Guzmán, Carlos F Ibáñez. Nat Neurosci 2007
6
Biology of GDNF and its receptors - Relevance for disorders of the central nervous system.
Carlos F Ibáñez, Jaan-Olle Andressoo. Neurobiol Dis 2017
Carlos F Ibáñez, Jaan-Olle Andressoo. Neurobiol Dis 2017
6
Development and evolution of the human neocortex.
Jan H Lui, David V Hansen, Arnold R Kriegstein. Cell 2011
Jan H Lui, David V Hansen, Arnold R Kriegstein. Cell 2011
6
The Changing Epidemiology of Autism Spectrum Disorders.
Kristen Lyall, Lisa Croen, Julie Daniels, M Daniele Fallin, Christine Ladd-Acosta, Brian K Lee, Bo Y Park, Nathaniel W Snyder, Diana Schendel, Heather Volk,[...]. Annu Rev Public Health 2017
Kristen Lyall, Lisa Croen, Julie Daniels, M Daniele Fallin, Christine Ladd-Acosta, Brian K Lee, Bo Y Park, Nathaniel W Snyder, Diana Schendel, Heather Volk,[...]. Annu Rev Public Health 2017
6
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
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
6
The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses.
Gil Stelzer, Naomi Rosen, Inbar Plaschkes, Shahar Zimmerman, Michal Twik, Simon Fishilevich, Tsippi Iny Stein, Ron Nudel, Iris Lieder, Yaron Mazor,[...]. Curr Protoc Bioinformatics 2016
Gil Stelzer, Naomi Rosen, Inbar Plaschkes, Shahar Zimmerman, Michal Twik, Simon Fishilevich, Tsippi Iny Stein, Ron Nudel, Iris Lieder, Yaron Mazor,[...]. Curr Protoc Bioinformatics 2016
6
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
G Bradley Schaefer, Nancy J Mendelsohn. Genet Med 2013
G Bradley Schaefer, Nancy J Mendelsohn. Genet Med 2013
6
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.