A citation-based method for searching scientific literature

Brenda M Finucane, David H Ledbetter, Jacob As Vorstman. Curr Opin Genet Dev 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.
A Jeremy Willsey, Montana T Morris, Sheng Wang, Helen R Willsey, Nawei Sun, Nia Teerikorpi, Tierney B Baum, Gerard Cagney, Kevin J Bender, Tejal A Desai,[...]. Cell 2018
50
100

The role of CNVs in the etiology of rare autosomal recessive disorders: the example of TRAPPC9-associated intellectual disability.
Jérémie Mortreux, Tiffany Busa, Dominique P Germain, Gwenaël Nadeau, Jacques Puechberty, Christine Coubes, Vincent Gatinois, Pierre Cacciagli, Yannis Duffourd, Jean-Marc Pinard,[...]. Eur J Hum Genet 2018
10
50

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
50

Novel Compound Heterozygous Mutations in the TRAPPC9 Gene in Two Siblings With Autism and Intellectual Disability.
Areerat Hnoonual, Potchanapond Graidist, Supika Kritsaneepaiboon, Pornprot Limprasert. Front Genet 2019
10
50

The Ensembl Variant Effect Predictor.
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
50

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban,[...]. Mol Psychiatry 2014
226
50

Mapping a shared genetic basis for neurodevelopmental disorders.
Matthew Jensen, Santhosh Girirajan. Genome Med 2017
13
50

Trappc9 deficiency in mice impairs learning and memory by causing imbalance of dopamine D1 and D2 neurons.
Yuting Ke, Meiqian Weng, Gaurav Chhetri, Muhammad Usman, Yan Li, Qing Yu, Yingzhuo Ding, Zejian Wang, Xiaolong Wang, Pinky Sultana,[...]. Sci Adv 2020
2
50

The TRAPP complex: insights into its architecture and function.
Michael Sacher, Yeon-Gil Kim, Arnon Lavie, Byung-Ha Oh, Nava Segev. Traffic 2008
92
50

Expression and function of NIK- and IKK2-binding protein (NIBP) in mouse enteric nervous system.
Y Zhang, D Bitner, A A Pontes Filho, F Li, S Liu, H Wang, F Yang, S Adhikari, J Gordon, S Srinivasan,[...]. Neurogastroenterol Motil 2014
14
50



Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications.
Xiaoyu Chen, Ole Schulz-Trieglaff, Richard Shaw, Bret Barnes, Felix Schlesinger, Morten Källberg, Anthony J Cox, Semyon Kruglyak, Christopher T Saunders. Bioinformatics 2016
462
50

An assessment of sex bias in neurodevelopmental disorders.
Andrew Polyak, Jill A Rosenfeld, Santhosh Girirajan. Genome Med 2015
40
50

TRAPPing a neurological disorder: from yeast to humans.
Zhanna Lipatova, Nicole Van Bergen, Daniela Stanga, Michael Sacher, John Christodoulou, Nava Segev. Autophagy 2020
6
50

Neurodevelopmental Disorders: From Genetics to Functional Pathways.
Ilaria Parenti, Luis G Rabaneda, Hanna Schoen, Gaia Novarino. Trends Neurosci 2020
28
50

Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010.
Harvey A Whiteford, Louisa Degenhardt, Jürgen Rehm, Amanda J Baxter, Alize J Ferrari, Holly E Erskine, Fiona J Charlson, Rosana E Norman, Abraham D Flaxman, Nicole Johns,[...]. Lancet 2013
50

Understanding Neurodevelopmental Disorders: The Promise of Regulatory Variation in the 3'UTRome.
Kai A Wanke, Paolo Devanna, Sonja C Vernes. Biol Psychiatry 2018
18
50



Genetic studies in intellectual disability and related disorders.
Lisenka E L M Vissers, Christian Gilissen, Joris A Veltman. Nat Rev Genet 2016
311
50

A structural variation reference for medical and population genetics.
Ryan L Collins, Harrison Brand, Konrad J Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C Francioli, Amit V Khera, Chelsea Lowther, Laura D Gauthier, Harold Wang,[...]. Nature 2020
106
50

Emerging role of NIK/IKK2-binding protein (NIBP)/trafficking protein particle complex 9 (TRAPPC9) in nervous system diseases.
Brittany Bodnar, Arianna DeGruttola, Yuanjun Zhu, Yuan Lin, Yonggang Zhang, Xianming Mo, Wenhui Hu. Transl Res 2020
4
50


Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in Drosophila.
Marieke Klein, Euginia L Singgih, Anne van Rens, Ditte Demontis, Anders D Børglum, Nina Roth Mota, Anna Castells-Nobau, Lambertus A Kiemeney, Han G Brunner, Alejandro Arias-Vasquez,[...]. Am J Psychiatry 2020
7
50

TRAPPC9: Novel insights into its trafficking and signaling pathways in health and disease (Review).
Thomas Mbimba, Nazar J Hussein, Ayesha Najeed, Fayez F Safadi. Int J Mol Med 2018
8
50

Spectrum of clinical heterogeneity of β-tubulin TUBB5 gene mutations.
I Madrigal, R Rabionet, M I Alvarez-Mora, A Sanchez, L Rodríguez-Revenga, X Estivill, M Mila. Gene 2019
5
50

[Diagnosis of a case with mental retardation due to novel compound heterozygous variants of TRAPPC9 gene].
Zhouxian Bai, Xiangdong Kong. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2019
4
50

Phenotypes in siblings with homozygous mutations of TRAPPC9 and/or MCPH1 support a bifunctional model of MCPH1.
Sarah Duerinckx, Marije Meuwissen, Camille Perazzolo, Laurence Desmyter, Isabelle Pirson, Marc Abramowicz. Mol Genet Genomic Med 2018
7
50

Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data.
Valentina Boeva, Tatiana Popova, Kevin Bleakley, Pierre Chiche, Julie Cappo, Gudrun Schleiermacher, Isabelle Janoueix-Lerosey, Olivier Delattre, Emmanuel Barillot. Bioinformatics 2012
444
50

High Incidence of Copy Number Variants in Adults with Intellectual Disability and Co-morbid Psychiatric Disorders.
Marina Viñas-Jornet, Susanna Esteba-Castillo, Neus Baena, Núria Ribas-Vidal, Anna Ruiz, David Torrents-Rodas, Elisabeth Gabau, Elisabet Vilella, Lourdes Martorell, Lluís Armengol,[...]. Behav Genet 2018
7
50

Molecular diagnostic experience of whole-exome sequencing in adult patients.
Jennifer E Posey, Jill A Rosenfeld, Regis A James, Matthew Bainbridge, Zhiyv Niu, Xia Wang, Shweta Dhar, Wojciech Wiszniewski, Zeynep H C Akdemir, Tomasz Gambin,[...]. Genet Med 2016
115
50

Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability.
Felippe Borlot, Bruno Ivo de Almeida, Shari L Combe, Danielle M Andrade, Francis M Filloux, Kenneth A Myers. Epilepsia 2019
14
50


Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.
Alice Poisson, Nicolas Chatron, Audrey Labalme, Pierre Fourneret, Dorothée Ville, Marie Laure Mathieu, Damien Sanlaville, Caroline Demily, Gaëtan Lesca. BMC Med Genet 2020
1
100

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock,[...]. Genet Med 2019
98
50

Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.
S Anazi, S Maddirevula, E Faqeih, H Alsedairy, F Alzahrani, H E Shamseldin, N Patel, M Hashem, N Ibrahim, F Abdulwahab,[...]. Mol Psychiatry 2017
105
50

Prevalence of co-occurring psychiatric disorders in adults and adolescents with intellectual disability: A systematic review and meta-analysis.
Mario G Mazza, Aurora Rossetti, Giovanna Crespi, Massimo Clerici. J Appl Res Intellect Disabil 2020
7
50

Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia.
Boris Chaumette, Vladimir Ferrafiat, Amirthagowri Ambalavanan, Alice Goldenberg, Alexandre Dionne-Laporte, Dan Spiegelman, Patrick A Dion, Priscille Gerardin, Claudine Laurent, David Cohen,[...]. Mol Psychiatry 2020
17
50

14-3-3ε and ζ regulate neurogenesis and differentiation of neuronal progenitor cells in the developing brain.
Kazuhito Toyo-oka, Tomoka Wachi, Robert F Hunt, Scott C Baraban, Shinichiro Taya, Hayley Ramshaw, Kozo Kaibuchi, Quenten P Schwarz, Angel F Lopez, Anthony Wynshaw-Boris. J Neurosci 2014
65
50

Characterization of intellectual disability and autism comorbidity through gene panel sequencing.
Maria C Aspromonte, Mariagrazia Bellini, Alessandra Gasparini, Marco Carraro, Elisa Bettella, Roberta Polli, Federica Cesca, Stefania Bigoni, Stefania Boni, Ombretta Carlet,[...]. Hum Mutat 2019
17
50

Ablation of the 14-3-3gamma Protein Results in Neuronal Migration Delay and Morphological Defects in the Developing Cerebral Cortex.
Tomoka Wachi, Brett Cornell, Courtney Marshall, Vladimir Zhukarev, Peter W Baas, Kazuhito Toyo-oka. Dev Neurobiol 2016
14
50

Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.
Johan H Thygesen, Kate Wolfe, Andrew McQuillin, Marina Viñas-Jornet, Neus Baena, Nathalie Brison, Greet D'Haenens, Susanna Esteba-Castillo, Elisabeth Gabau, Núria Ribas-Vidal,[...]. Br J Psychiatry 2018
11
50

Psychiatric Comorbidity in Older Adults with Intellectual Disability.
Agnieszka Bratek, Krzysztof Krysta, Krzysztof Kucia. Psychiatr Danub 2017
6
50

Copy Number Variation in Syndromic Forms of Psychiatric Illness: The Emerging Value of Clinical Genetic Testing in Psychiatry.
Christian G Bouwkamp, Anneke J A Kievit, Sander Markx, Joseph I Friedman, Laura van Zutven, Rick van Minkelen, Terry Vrijenhoek, Bin Xu, Ineke Sterrenburg-van de Nieuwegiessen, Joris A Veltman,[...]. Am J Psychiatry 2017
9
50


Psychiatric manifestations revealing inborn errors of metabolism in adolescents and adults.
F Sedel, N Baumann, J-C Turpin, O Lyon-Caen, J-M Saudubray, D Cohen. J Inherit Metab Dis 2007
97
50

[Editorial: Medical ethics in medical care services].
P Kassab. AMB Rev Assoc Med Bras 1973
64
50

Mental ill-health in adults with intellectual disabilities: prevalence and associated factors.
Sally-Ann Cooper, Elita Smiley, Jillian Morrison, Andrew Williamson, Linda Allan. Br J Psychiatry 2007
459
50



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.