A citation-based method for searching scientific literature

J R M Ceroni, R L Dutra, R S Honjo, J C Llerena, A X Acosta, P F V Medeiros, M F Galera, É A Zanardo, F B Piazzon, A T Dias, G M Novo-Filho, M M Montenegro, F A R Madia, D R Bertola, J B de Melo, L D Kulikowski, C A Kim. Sci Rep 2018
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
79
100


Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing.
Makenzie Saoura, Christopher A Powell, Robert Kopajtich, Ahmad Alahmad, Haya H Al-Balool, Buthaina Albash, Majid Alfadhel, Charlotte L Alston, Enrico Bertini, Penelope E Bonnen,[...]. Hum Mutat 2019
10
100

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
417
100

Array-CGH analysis in patients with intellectual disability and/or congenital malformations in Brazil.
G S Vianna, P F V Medeiros, A F Alves, T O Silva, F S Jehee. Genet Mol Res 2016
7
100

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
290
100

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis.
Lisenka E L M Vissers, Bert B A de Vries, Joris A Veltman. J Med Genet 2010
107
100

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies.
Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C Rivera, María L Guzmán, Gabriela M Repetto. J Pediatr (Rio J) 2015
6
100

An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficits.
Michael J Doherty, Ian A Glass, Craig L Bennett, Phil D Cotter, Nate F Watson, Anna L Mitchell, Tom D Bird, Don F Farrell. Epilepsia 2003
35
100

Clinical and molecular characterization of duplications encompassing the human SHOX gene reveal a variable effect on stature.
N Simon Thomas, John F Harvey, David J Bunyan, Julia Rankin, Giedre Grigelioniene, Damien L Bruno, Tiong Y Tan, Susan Tomkins, Robert Hastings. Am J Med Genet A 2009
39
100

Unmasking a Case of Asymptomatic Charcot-Marie-Tooth Disease (CMT1A) With Vincristine.
Roopam Jariwal, Basel Shoua, Katayoun Sabetian, Piruthiviraj Natarajan, Everardo Cobos. J Investig Med High Impact Case Rep 2018
4
100

Analysis of a Protein Network Related to Copy Number Variations in Autism Spectrum Disorder.
Jaqueline B Schuch, Vanessa R Paixão-Côrtes, Dânae Longo, Tatiana Roman, Rudimar Dos S Riesgo, Josiane Ranzan, Michele M Becker, Mariluce Riegel, Lavinia Schuler-Faccini. J Mol Neurosci 2019
3
100

The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 Mutation.
Zarghuna M A Shinwari, Abdulrahman Almesned, Ali Alakhfash, Ahmad M Al-Rashdan, Eissa Faqeih, Zainab Al-Humaidi, Ahmed Alomrani, Malak Alghamdi, Dilek Colak, Abdullah Alwadai,[...]. Cardiology 2017
11
100

Analysis of chromosomal abnormalities by CGH-array in patients with dysmorphic and intellectual disability with normal karyotype.
Rodrigo Pratte-Santos, Katyanne Heringer Ribeiro, Thainá Altoe Santos, Terezinha Sarquis Cintra. Einstein (Sao Paulo) 2016
4
100

Cryptic chromosomal rearrangements in children with idiopathic mental retardation in the Czech population.
Katerina Hirschfeldova, Alice Baxova, Vera Kebrdlova, Roman Solc, Romana Mihalova, Petr Lnenicka, Kamila Vesela, Jitka Stekrova. Genet Test Mol Biomarkers 2011
3
100

A parallel study of different array-CGH platforms in a set of Spanish patients with developmental delay and intellectual disability.
Laia Rodríguez-Revenga, Elena Vallespín, Irene Madrigal, María Palomares, Antonio Mur, Sixto García-Miñaur, Fernando Santos, M Ángeles Mori, Pablo Lapunzina, Montserrat Mila,[...]. Gene 2013
13
100

Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID.
Silke Redler, Tim M Strom, Thomas Wieland, Kirsten Cremer, Hartmut Engels, Felix Distelmaier, Jörg Schaper, Alma Küchler, Johannes R Lemke, Stephanie Jeschke,[...]. Eur J Hum Genet 2017
16
100

When phenotype does not match genotype: importance of "real-time" refining of phenotypic information for exome data interpretation.
Lina Basel-Salmon, Noa Ruhrman-Shahar, Naama Orenstein, Yael Goldberg, Claudia Gonzaga-Jauregui, Alan R Shuldiner, Rivka Sukenik-Halevy, Idit Maya, Nurit Magal, Ofir Hagari,[...]. Genet Med 2021
3
100

16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders.
Arivudainambi Ramalingam, Xin-Gang Zhou, Stephanie D Fiedler, Sarah J Brawner, Julie M Joyce, Hong-Yu Liu, Shihui Yu. J Hum Genet 2011
71
100

A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD.
Kym M Boycott, Malcolm I Parslow, Judith L Ross, Ivan P Miller, N Torben Bech-Hansen, Patrick M MacLeod. Am J Med Genet A 2003
27
100


Charcot-Marie-Tooth hereditary neuropathy revealed after administration of docetaxel in advanced breast cancer.
Hampig Raphael Kourie, Nicolas Mavroudakis, Philippe Aftimos, Martine Piccart. World J Clin Oncol 2017
3
100

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.
David A Koolen, Rolph Pfundt, Nicole de Leeuw, Jayne Y Hehir-Kwa, Willy M Nillesen, Ineke Neefs, Ine Scheltinga, Erik Sistermans, Dominique Smeets, Han G Brunner,[...]. Hum Mutat 2009
113
100

The human clinical phenotypes of altered CHRNA7 copy number.
Madelyn A Gillentine, Christian P Schaaf. Biochem Pharmacol 2015
57
100

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
149
100

High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?
Idit Maya, Lina Basel-Salmon, Ami Singer, Lena Sagi-Dain. Genet Med 2020
3
100

The genetic basis of non-syndromic intellectual disability: a review.
Liana Kaufman, Muhammad Ayub, John B Vincent. J Neurodev Disord 2010
135
100

Triplication of 16p12.1p12.3 associated with developmental and growth delay and distinctive facial features.
Graeme A M Nimmo, Andrea Guerin, Ramses Badilla-Porras, Dimitri J Stavropoulos, Grace Yoon, Melissa T Carter. Am J Med Genet A 2016
2
100

Association between the thrombophilic polymorphisms MTHFR C677T, Factor V Leiden, and prothrombin G20210A and recurrent miscarriage in Brazilian women.
R O Gonçalves, L R Fraga, W V B Santos, A F L Carvalho, B A V Veloso Cerqueira, M Sarno, M B P Toralles, M J Vieira, C G Dutra, L Schüler-Faccini,[...]. Genet Mol Res 2016
6
100

Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
M Shoukier, N Klein, B Auber, J Wickert, J Schröder, B Zoll, P Burfeind, I Bartels, E A Alsat, M Lingen,[...]. Clin Genet 2013
45
100


Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders From the South of Brazil.
Tiago Fernando Chaves, Nathacha Baretto, Luan Freitas de Oliveira, Maristela Ocampos, Ingrid Tremel Barbato, Mayara Anselmi, Gisele Rozone De Luca, Jorge Humberto Barbato Filho, Louise Lapagesse de Camargo Pinto, Pricila Bernardi,[...]. Sci Rep 2019
4
100

Screening for intellectual disability using high-resolution CMA technology in a retrospective cohort from Central Brazil.
Rodrigo Roncato Pereira, Irene Plaza Pinto, Lysa Bernardes Minasi, Aldaires Vieira de Melo, Damiana Mirian da Cruz e Cunha, Alex Silva Cruz, Cristiano Luiz Ribeiro, Cláudio Carlos da Silva, Daniela de Melo e Silva, Aparecido Divino da Cruz. PLoS One 2014
5
100

Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands.
Ron Hochstenbach, Ellen van Binsbergen, John Engelen, Aggie Nieuwint, Abeltje Polstra, Pino Poddighe, Claudia Ruivenkamp, Birgit Sikkema-Raddatz, Dominique Smeets, Martin Poot. Eur J Med Genet 2009
126
100



Variation in the influence of selected sociodemographic risk factors for mental retardation.
C D Drews, M Yeargin-Allsopp, P Decouflé, C C Murphy. Am J Public Health 1995
76
100

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
100

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
Reinhard Ullmann, Gillian Turner, Maria Kirchhoff, Wei Chen, Bruce Tonge, Carla Rosenberg, Michael Field, Angela M Vianna-Morgante, Louise Christie, Ana C Krepischi-Santos,[...]. Hum Mutat 2007
208
100

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?
Przemyslaw Szafranski, Christian P Schaaf, Richard E Person, Ian B Gibson, Zhilian Xia, Sangeetha Mahadevan, Joanna Wiszniewska, Carlos A Bacino, Seema Lalani, Lorraine Potocki,[...]. Hum Mutat 2010
97
100

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Karen S Ho, E Robert Wassman, Adrianne L Baxter, Charles H Hensel, Megan M Martin, Aparna Prasad, Hope Twede, Rena J Vanzo, Merlin G Butler. Int J Mol Sci 2016
27
100

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease.
Heather C Mefford, Gregory M Cooper, Troy Zerr, Joshua D Smith, Carl Baker, Neil Shafer, Erik C Thorland, Cindy Skinner, Charles E Schwartz, Deborah A Nickerson,[...]. Genome Res 2009
102
100

A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement.
Nadia A Akawi, Salma Ben-Salem, Jozef Hertecant, Anne John, Thachillath Pramathan, Praseetha Kizhakkedath, Bassam R Ali, Lihadh Al-Gazali. Orphanet J Rare Dis 2016
8
100

Customized high resolution CGH-array for clinical diagnosis reveals additional genomic imbalances in previous well-defined pathological samples.
Elena Vallespín, María Palomares Bralo, M Ángeles Mori, Rubén Martín, Sixto García-Miñaúr, Luis Fernández, M Luisa de Torres, Fe García-Santiago, Elena Mansilla, Fernando Santos,[...]. Am J Med Genet A 2013
23
100

A duplication encompassing the SHOX gene and the downstream evolutionarily conserved sequences.
Laura Roos, Karen Brøndum Nielsen, Zeynep Tümer. Am J Med Genet A 2009
14
100

Clinical and molecular evaluation of SHOX/PAR1 duplications in Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS).
S Benito-Sanz, E Barroso, D Heine-Suñer, A Hisado-Oliva, V Romanelli, J Rosell, A Aragones, M Caimari, J Argente, J L Ross,[...]. J Clin Endocrinol Metab 2011
52
100

Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traits.
Elisa Tassano, Andrea Accogli, Marco Pavanello, Claudio Bruno, Valeria Capra, Giorgio Gimelli, Cristina Cuoco. Eur J Med Genet 2016
9
100

[16p11.2 Microdeletion: first report in Argentina].
Agostina Tardivo, Bárbara Masotto, Lucía Espeche, Andrea P Solari, Julián Nevado, Sandra Rozental. Arch Argent Pediatr 2017
2
100


Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.
A C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, M R Passos-Bueno, J Knijnenburg, K Szuhai, W Sloos, J F Mazzeu, F Kok, C Cheroki,[...]. Cytogenet Genome Res 2006
86
100


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.