A citation-based method for searching scientific literature

Christopher W Fell, Vanja Nagy. Trends Mol Med 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


The Use of Next-Generation Sequencing for Research and Diagnostics for Intellectual Disability.
Ricardo Harripaul, Abdul Noor, Muhammad Ayub, John B Vincent. Cold Spring Harb Perspect Med 2017
27
75

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
75

Genetic studies in intellectual disability and related disorders.
Lisenka E L M Vissers, Christian Gilissen, Joris A Veltman. Nat Rev Genet 2016
367
50

Genetics of intellectual disability.
H Hilger Ropers. Curr Opin Genet Dev 2008
118
50

Genetic testing in children and adolescents with intellectual disability.
Nick Bass, David Skuse. Curr Opin Psychiatry 2018
11
50

Human Models Are Needed for Studying Human Neurodevelopmental Disorders.
Xinyu Zhao, Anita Bhattacharyya. Am J Hum Genet 2018
50
50

Next-generation sequencing approaches and challenges in the diagnosis of developmental anomalies and intellectual disability.
Ange-Line Bruel, Antonio Vitobello, Frédéric Tran Mau-Them, Sophie Nambot, Arthur Sorlin, Anne-Sophie Denommé-Pichon, Julian Delanne, Sébastien Moutton, Patrick Callier, Yannis Duffourd,[...]. Clin Genet 2020
8
50

Genetics of early onset cognitive impairment.
Hans Hilger Ropers. Annu Rev Genomics Hum Genet 2010
236
50

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
175
50

Discontinuity in the genetic and environmental causes of the intellectual disability spectrum.
Abraham Reichenberg, Martin Cederlöf, Andrew McMillan, Maciej Trzaskowski, Ori Kapra, Eyal Fruchter, Karen Ginat, Michael Davidson, Mark Weiser, Henrik Larsson,[...]. Proc Natl Acad Sci U S A 2016
49
50

A clinical primer on intellectual disability.
Dilip R Patel, Maria Demma Cabral, Arlene Ho, Joav Merrick. Transl Pediatr 2020
18
50

Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.
Korinna Kochinke, Christiane Zweier, Bonnie Nijhof, Michaela Fenckova, Pavel Cizek, Frank Honti, Shivakumar Keerthikumar, Merel A W Oortveld, Tjitske Kleefstra, Jamie M Kramer,[...]. Am J Hum Genet 2016
139
50



Phenotypic and genotypic characterization of families with complex intellectual disability identified pathogenic genetic variations in known and novel disease genes.
Hossein Darvish, Luis J Azcona, Abbas Tafakhori, Roxana Mesias, Azadeh Ahmadifard, Elena Sanchez, Arman Habibi, Elham Alehabib, Amir Hossein Johari, Babak Emamalizadeh,[...]. Sci Rep 2020
6
50

Advances in understanding - genetic basis of intellectual disability.
Pietro Chiurazzi, Filomena Pirozzi. F1000Res 2016
60
50


Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders.
Caroline F Wright, Jeremy F McRae, Stephen Clayton, Giuseppe Gallone, Stuart Aitken, Tomas W FitzGerald, Philip Jones, Elena Prigmore, Diana Rajan, Jenny Lord,[...]. Genet Med 2018
152
50

Genomic diagnosis for children with intellectual disability and/or developmental delay.
Kevin M Bowling, Michelle L Thompson, Michelle D Amaral, Candice R Finnila, Susan M Hiatt, Krysta L Engel, J Nicholas Cochran, Kyle B Brothers, Kelly M East, David E Gray,[...]. Genome Med 2017
113
50

Genome sequencing identifies major causes of severe intellectual disability.
Christian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W M van Bon, Marjolein H Willemsen, Michael Kwint, Irene M Janssen, Alexander Hoischen, Annette Schenck,[...]. Nature 2014
691
50

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
50

15q13.3 duplication in two patients with childhood-onset schizophrenia.
Dale Zhou, Peter Gochman, Diane D Broadnax, Judith L Rapoport, Kwangmi Ahn. Am J Med Genet B Neuropsychiatr Genet 2016
19
25


Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
186
25

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.
Dinka Smajlagić, Ksenia Lavrichenko, Siren Berland, Øyvind Helgeland, Gun Peggy Knudsen, Marc Vaudel, Jan Haavik, Per Morten Knappskog, Pål Rasmus Njølstad, Gunnar Houge,[...]. Eur J Hum Genet 2021
10
25

Clinical study and PLA2G6 mutation screening analysis in Chinese patients with infantile neuroaxonal dystrophy.
Y Wu, Y Jiang, Z Gao, J Wang, Y Yuan, H Xiong, X Chang, X Bao, Y Zhang, J Xiao,[...]. Eur J Neurol 2009
41
25

19q13.32 microdeletion syndrome: three new cases.
Angela Castillo, Nancy Kramer, Charles E Schwartz, Judith H Miles, Barbara R DuPont, Jill A Rosenfeld, John M Graham. Eur J Med Genet 2014
14
25

Comprehensive genomic analysis of patients with disorders of cerebral cortical development.
Wojciech Wiszniewski, Pawel Gawlinski, Tomasz Gambin, Monika Bekiesinska-Figatowska, Ewa Obersztyn, Dorota Antczak-Marach, Zeynep Hande Coban Akdemir, Tamar Harel, Ender Karaca, Marta Jurek,[...]. Eur J Hum Genet 2018
17
25


Duplication of 10q24 locus: broadening the clinical and radiological spectrum.
Muriel Holder-Espinasse, Aleksander Jamsheer, Fabienne Escande, Joris Andrieux, Florence Petit, Anna Sowinska-Seidler, Magdalena Socha, Anna Jakubiuk-Tomaszuk, Marion Gerard, Michèle Mathieu-Dramard,[...]. Eur J Hum Genet 2019
4
25

Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders.
Wei-Hsien Chien, Susan Shur-Fen Gau, Hsiao-Mei Liao, Yen-Nan Chiu, Yu-Yu Wu, Yu-Shu Huang, Wen-Che Tsai, Ho-Min Tsai, Chia-Hsiang Chen. Mol Autism 2013
34
25

A novel 5q35.3 subtelomeric deletion syndrome.
Anita Rauch, Maike Beese, Ertan Mayatepek, Helmut-Günther Dörr, Dieter Wenzel, André Reis, Udo Trautmann. Am J Med Genet A 2003
22
25

CNV profiles of Chinese pediatric patients with developmental disorders.
Haiming Yuan, Shaofang Shangguan, Zhengchang Li, Jingsi Luo, Jiasun Su, Ruen Yao, Shun Zhang, Chen Liang, Qian Chen, Zhijie Gao,[...]. Genet Med 2021
8
25

Chromosome 7q22-q31 duplication: report of a new case and review.
A Mégarbané, P Gosset, N Souraty, J M Lapierre, C Turleau, M Vekemans, J Loiselet, M Prieur. Am J Med Genet 2000
11
25

Diagnostic yield of array comparative genomic hybridization in adults with autism spectrum disorders.
Gary Stobbe, Yajuan Liu, Rebecca Wu, Laura Heath Hudgings, Owen Thompson, Fuki M Hisama. Genet Med 2014
14
25

Copy-number variants in neurodevelopmental disorders: promises and challenges.
Alison K Merikangas, Aiden P Corvin, Louise Gallagher. Trends Genet 2009
89
25

Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH).
Jennifer R Toone, Derek A Applegarth, Harvey L Levy, Marion B Coulter-Mackie, Gary Lee. Mol Genet Metab 2003
10
25

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.
Gurdeep S Sagoo, Adam S Butterworth, Simon Sanderson, Charles Shaw-Smith, Julian P T Higgins, Hilary Burton. Genet Med 2009
150
25

A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia.
S Kure, T Shinka, Y Sakata, N Osamu, M Takayanagi, K Tada, Y Matsubara, K Narisawa. J Hum Genet 1998
17
25

Molecular analysis in 23 Hunter disease families.
W Lissens, S Seneca, I Liebaers. J Inherit Metab Dis 1997
23
25

Clinical description of a patient carrying the smallest reported deletion involving 10p14 region.
Daniela Melis, Rita Genesio, Pasquale Boemio, Ennio Del Giudice, Gerarda Cappuccio, Angela Mormile, Valentina Ronga, Anna Conti, Floriana Imperati, Lucio Nitsch,[...]. Am J Med Genet A 2012
19
25

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H Al Turki, Bernard Thienpont, Jeremy McRae, Tomas W Fitzgerald, Tarjinder Singh, Ganesh Jawahar Swaminathan,[...]. Nat Genet 2016
198
25

De novo 8p23.1 deletion in a patient with absence epilepsy.
Nihan Hande Akcakaya, Özlem Yalcin Capan, Herbert Schulz, Thomas Sander, Server Hande Caglayan, Zuhal Yapıcı. Epileptic Disord 2017
4
25

An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis.
Liangjing Chen, Andrew Hadd, Sachin Sah, Stela Filipovic-Sadic, Julie Krosting, Edward Sekinger, Ruiqin Pan, Paul J Hagerman, Timothy T Stenzel, Flora Tassone,[...]. J Mol Diagn 2010
133
25

Karyotype versus genomic hybridization for the prenatal diagnosis of chromosomal abnormalities: a metaanalysis.
Wilmar Saldarriaga, Herney Andrés García-Perdomo, Johanna Arango-Pineda, Javier Fonseca. Am J Obstet Gynecol 2015
23
25

9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression.
Maria Teresa Bonati, Chiara Castronovo, Alessandra Sironi, Dario Zimbalatti, Ilaria Bestetti, Milena Crippa, Antonio Novelli, Sara Loddo, Maria Lisa Dentici, Juliet Taylor,[...]. Neurogenetics 2019
7
25


2q31.1 microdeletion syndrome: redefining the associated clinical phenotype.
Boyan Dimitrov, Irina Balikova, Thomy de Ravel, Hilde Van Esch, Maryse De Smedt, Emiel Baten, Joris Robert Vermeesch, Irena Bradinova, Emil Simeonov, Koen Devriendt,[...]. J Med Genet 2011
21
25

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
25

Duplication of the distal long arm of chromosome 15: report of three new patients and review of the literature.
Jennifer A Roggenbuck, Nancy J Mendelsohn, Beverly Tenenholz, Roger L Ladda, James M Fink. Am J Med Genet A 2004
22
25


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.