A citation-based method for searching scientific literature

G S Vianna, P F V Medeiros, A F Alves, T O Silva, F S Jehee. Genet Mol Res 2016
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
71

Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
E Di Gregorio, E Riberi, E F Belligni, E Biamino, M Spielmann, U Ala, A Calcia, I Bagnasco, D Carli, G Gai,[...]. Clin Genet 2017
24
57

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
75

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
50

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
533
42

New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Gerarda Cappuccio, Francesco Vitiello, Alberto Casertano, Paolo Fontana, Rita Genesio, Dario Bruzzese, Virginia Maria Ginocchio, Angela Mormile, Lucio Nitsch, Generoso Andria,[...]. Ital J Pediatr 2016
10
42

Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patients.
Joo Wook Ahn, Susan Bint, Anne Bergbaum, Kathy Mann, Richard P Hall, Caroline Mackie Ogilvie. Mol Cytogenet 2013
37
28

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
28


Considering specific clinical features as evidence of pathogenic copy number variants.
Egle Preiksaitiene, Alma Molytė, Jurate Kasnauskiene, Zivile Ciuladaite, Algirdas Utkus, Philippos C Patsalis, Vaidutis Kučinskas. J Appl Genet 2014
12
28

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
28


Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.
Joris R Vermeesch, Paul D Brady, Damien Sanlaville, Klaas Kok, Rosalind J Hastings. Hum Mutat 2012
54
28

The Diagnostic Yield of Array Comparative Genomic Hybridization Is High Regardless of Severity of Intellectual Disability/Developmental Delay in Children.
Stefano D'Arrigo, Francesco Gavazzi, Enrico Alfei, Orsetta Zuffardi, Cristina Montomoli, Barbara Corso, Erika Buzzi, Francesca L Sciacca, Sara Bulgheroni, Daria Riva,[...]. J Child Neurol 2016
22
28

Phenotype profiling of patients with intellectual disability and copy number variations.
Mónica Roselló, Francisco Martínez, Sandra Monfort, Sonia Mayo, Silvestre Oltra, Carmen Orellana. Eur J Paediatr Neurol 2014
10
28

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
28

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.
Magdalena Bartnik, Beata Nowakowska, Katarzyna Derwińska, Barbara Wiśniowiecka-Kowalnik, Marta Kędzior, Joanna Bernaciak, Kamila Ziemkiewicz, Tomasz Gambin, Maciej Sykulski, Natalia Bezniakow,[...]. J Appl Genet 2014
30
28

Copy number variation analysis of patients with intellectual disability from North-West Spain.
Inés Quintela, Jesús Eirís, Carmen Gómez-Lado, Laura Pérez-Gay, David Dacruz, Raquel Cruz, Manuel Castro-Gago, Luz Míguez, Ángel Carracedo, Francisco Barros. Gene 2017
11
28

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
40

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
Guylaine D'Amours, Mathieu Langlois, Géraldine Mathonnet, Raouf Fetni, Sonia Nizard, Myriam Srour, Frédérique Tihy, Michael S Phillips, Jacques L Michaud, Emmanuelle Lemyre. BMC Med Genomics 2014
11
28

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
28

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
28

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
28

Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries.
Fernanda Sarquis Jehee, Jean Tetsuo Takamori, Paula F Vasconcelos Medeiros, Ana Carolina B Pordeus, Flavia Roche M Latini, Débora Romeo Bertola, Chong Ae Kim, Maria Rita Passos-Bueno. Eur J Med Genet 2011
31
14

Developmental evaluation of aldo-keto reductase 1C3 expression in the cryptorchid testis.
Richard A Ashley, Zhongxin Yu, Kar-Ming Fung, Dominic Frimberger, Bradley P Kropp, Trevor M Penning, Hsueh-Kung Lin. Urology 2010
9
14

5p deletions: Current knowledge and future directions.
Joanne M Nguyen, Krista J Qualmann, Rebecca Okashah, AmySue Reilly, Mikhail F Alexeyev, Dennis J Campbell. Am J Med Genet C Semin Med Genet 2015
38
14

Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes.
Chih-Ping Chen, Ming-Chao Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang. Gene 2013
13
14

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases.
Sang-Jin Park, Eun Hye Jung, Ran-Suk Ryu, Hyun Woong Kang, Jung-Min Ko, Hyon J Kim, Chong Kun Cheon, Sang-Hyun Hwang, Ho-Young Kang. Mol Cytogenet 2011
60
14

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
Lina Shao, Chad A Shaw, Xin-Yan Lu, Trilochan Sahoo, Carlos A Bacino, Seema R Lalani, Pawel Stankiewicz, Svetlana A Yatsenko, Yinfeng Li, Sarah Neill,[...]. Am J Med Genet A 2008
89
14

Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe.
Diana Wellesley, Helen Dolk, Patricia A Boyd, Ruth Greenlees, Martin Haeusler, Vera Nelen, Ester Garne, Babak Khoshnood, Berenice Doray, Anke Rissmann,[...]. Eur J Hum Genet 2012
81
14

Cytogenetic and molecular characterization of a three-generation family with chromosome 5p terminal deletion.
J-S Fang, K-F Lee, C-T Huang, C-L Syu, K-J Yang, L-H Wang, D-L Liao, C-H Chen. Clin Genet 2008
10
14

Genetic Approach to Diagnosis of Intellectual Disability.
Ratna Dua Puri, Moni Tuteja, I C Verma. Indian J Pediatr 2016
7
14


Chromosome analysis: what and when to request.
F H Sharkey, E Maher, D R FitzPatrick. Arch Dis Child 2005
4
25


Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p.
Pankaj Sharma, Neerja Gupta, Madhumita R Chowdhury, Savita Sapra, Rashmi Shukla, Meena Lall, Madhulika Kabra. J Pediatr Genet 2013
3
33

A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome.
Amira Elmakky, Diana Carli, Licia Lugli, Paola Torelli, Battista Guidi, Cristina Falcinelli, Sergio Fini, Fabrizio Ferrari, Antonio Percesepe. Eur J Med Genet 2014
17
14

Reciprocal Translocation Carrier Diagnosis in Preimplantation Human Embryos.
Liang Hu, Dehua Cheng, Fei Gong, Changfu Lu, Yueqiu Tan, Keli Luo, Xianhong Wu, Wenbing He, Pingyuan Xie, Tao Feng,[...]. EBioMedicine 2016
26
14

Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies.
Daniel L Di Bartolo, Mohamed El Naggar, Renius Owen, Trilochan Sahoo, Fred Gilbert, Venkat R Pulijaal, Susan Mathew. Mol Cytogenet 2012
8
14



Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.
Ivan Y Iourov, Svetlana G Vorsanova, Oxana S Kurinnaia, Maria A Zelenova, Alexandra P Silvanovich, Yuri B Yurov. Mol Cytogenet 2012
39
14

Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter.
Daisuke Fukushi, Kenji Kurosawa, Yasuyo Suzuki, Kaoru Suzuki, Kenichiro Yamada, Seiji Watanabe, Kenji Yokochi, Nobuaki Wakamatsu. Am J Med Genet A 2017
1
100

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
18
14

Two novel familial balanced translocations t(8;11)(p23;q21) and t(6;16)(q26;p12) implicated in recurrent spontaneous abortion.
Fatemeh Keify, Narges Zhiyan, Farzaneh Mirzaei, Semiramis Tootian, Saeedeh Ghazaey, Mohammad R Abbaszadegan. Arch Iran Med 2012
6
16

De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age.
N Simon Thomas, Joan K Morris, Julia Baptista, Bee Ling Ng, John A Crolla, Patricia A Jacobs. J Med Genet 2010
30
14


Mapping 22q11.2 Gene Dosage Effects on Brain Morphometry.
Amy Lin, Christopher R K Ching, Ariana Vajdi, Daqiang Sun, Rachel K Jonas, Maria Jalbrzikowski, Leila Kushan-Wells, Laura Pacheco Hansen, Emma Krikorian, Boris Gutman,[...]. J Neurosci 2017
37
14

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.
Karin R Engelhardt, Sean McGhee, Sabine Winkler, Atfa Sassi, Cristina Woellner, Gabriela Lopez-Herrera, Andrew Chen, Hong Sook Kim, Maria Garcia Lloret, Ilka Schulze,[...]. J Allergy Clin Immunol 2009
321
14

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
14


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.