A citation-based method for searching scientific literature

Chung-Lin Lee, Chen-Hao Lee, Chih-Kuang Chuang, Huei-Ching Chiu, Yen-Jiun Chen, Chao-Ling Chou, Peih-Shan Wu, Chih-Ping Chen, Hsiang-Yu Lin, Shuan-Pei Lin. Pediatr Neonatol 2019
Times Cited: 2







List of co-cited articles
1 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
100

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
922
50

Chromosomal microarray analysis and prenatal diagnosis.
Jamie O Lo, Brian L Shaffer, Cori D Feist, Aaron B Caughey. Obstet Gynecol Surv 2014
14
50

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Ifaat Agmon-Fishman, Lital Cohen-Vig, Yael Goldberg, Racheli Berger,[...]. Genet Med 2018
27
50

European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities.
I Feenstra, J Fang, D A Koolen, A Siezen, C Evans, R M Winter, M M Lees, M Riegel, B B A de Vries, C M A Van Ravenswaaij,[...]. Eur J Med Genet 2006
60
50

A preliminary study of copy number variation in Tibetans.
Yong-Biao Zhang, Xin Li, Feng Zhang, Duen-Mei Wang, Jun Yu. PLoS One 2012
20
50

CircosVCF: circos visualization of whole-genome sequence variations stored in VCF files.
E Drori, D Levy, P Smirin-Yosef, O Rahimi, M Salmon-Divon. Bioinformatics 2017
9
50


dbVar structural variant cluster set for data analysis and variant comparison.
Lon Phan, Jeffrey Hsu, Le Quang Minh Tri, Michaela Willi, Tamer Mansour, Yan Kai, John Garner, John Lopez, Ben Busby. F1000Res 2016
11
50

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
920
50

Closing the gaps on human chromosome 19 revealed genes with a high density of repetitive tandemly arrayed elements.
Sun-Hee Leem, Natalay Kouprina, Jane Grimwood, Jung-Hyun Kim, Michael Mullokandov, Young-Ho Yoon, Ji-Youn Chae, Jenna Morgan, Susan Lucas, Paul Richardson,[...]. Genome Res 2004
29
50

Consanguinity in a population sample of Israeli Muslim Arabs, Christian Arabs and Druze.
R Vardi-Saliternik, Y Friedlander, T Cohen. Ann Hum Biol 2002
73
50

Copy number variations and genetic admixtures in three Xinjiang ethnic minority groups.
Haiyi Lou, Shilin Li, Wenfei Jin, Ruiqing Fu, Dongsheng Lu, Xinwei Pan, Huaigu Zhou, Yuan Ping, Li Jin, Shuhua Xu. Eur J Hum Genet 2015
16
50

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker,[...]. Prenat Diagn 2018
15
50

Marked yield of re-evaluating phenotype and exome/target sequencing data in 33 individuals with intellectual disabilities.
Bing Xiao, Wenjuan Qiu, Xing Ji, Xiaoqing Liu, Zhuo Huang, Huili Liu, Yanjie Fan, Yan Xu, Yu Liu, Hui Yie,[...]. Am J Med Genet A 2018
17
50

Characteristics and outcome of primary sclerosing cholangitis associated with inflammatory bowel disease in Asian children.
Way Seah Lee, Sivaramakrishnan Venkatesh Karthik, Ruey Terng Ng, Sik Yong Ong, Christina Ong, Fang K Chiou, Shin Yee Wong, Seng Hock Quak, Marion Margaret Aw. Pediatr Neonatol 2019
4
50

The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma.
Karen A Lapidos, Rahul Kakkar, Elizabeth M McNally. Circ Res 2004
323
50

An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder.
Leandro de Araújo Lima, Ana Cecília Feio-dos-Santos, Sintia Iole Belangero, Ary Gadelha, Rodrigo Affonseca Bressan, Giovanni Abrahão Salum, Pedro Mario Pan, Tais Silveira Moriyama, Ana Soledade Graeff-Martins, Ana Carina Tamanaha,[...]. Sci Rep 2016
10
50

A remark on copy number variation detection methods.
Shuo Li, Xialiang Dou, Ruiqi Gao, Xinzhou Ge, Minping Qian, Lin Wan. PLoS One 2018
7
50

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A Fasel, Ekaterina Batourina, Matthew G Sampson,[...]. Nat Genet 2019
46
50

Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.
Miriam Kessi, Juan Xiong, Liwen Wu, Lifen Yang, Fang He, Chen Chen, Nan Pang, Haolin Duan, Wen Zhang, Ahmed Arafat,[...]. Front Neurol 2018
10
50

Based on a cohort of 52,879 microarrays, recurrent intragenic FBN2 deletion encompassing exons 1-8 does not cause Beals syndrome.
Idit Maya, Sarit Kahana, Ifaat Agmon-Fishman, Cochava Klein, Reut Matar, Racheli Berger, Mordechai Shohat, Lina Basel-Salmon, Reuven Sharony, Lena Sagi-Dain. Eur J Med Genet 2020
2
50

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17.
P F Chance, N Abbas, M W Lensch, L Pentao, B B Roa, P I Patel, J R Lupski. Hum Mol Genet 1994
259
50

Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.
Jordi Soler, Lourdes Fañanás, Mara Parellada, Marie-Odile Krebs, Guy A Rouleau, Mar Fatjó-Vilas. J Psychiatry Neurosci 2018
20
50

Genetics and genomic medicine in Israel.
Joël Zlotogora. Mol Genet Genomic Med 2014
31
50

Drug resistance characteristics of Mycobacterium tuberculosis isolates between 2014 and 2017 in Sichuan, China: A retrospective study.
Mi Zhou, Shan Liu, Qingfeng Li, Qiming Wang, Ma Zhu, Ling Cao, Dongmei Wang, Yuanhong Xu, Tianli Zheng, Qian Ye,[...]. PLoS One 2018
6
50

CNV biology in neurodevelopmental disorders.
Toru Takumi, Kota Tamada. Curr Opin Neurobiol 2018
38
50

Counting the founders: the matrilineal genetic ancestry of the Jewish Diaspora.
Doron M Behar, Ene Metspalu, Toomas Kivisild, Saharon Rosset, Shay Tzur, Yarin Hadid, Guennady Yudkovsky, Dror Rosengarten, Luisa Pereira, Antonio Amorim,[...]. PLoS One 2008
64
50

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Lena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifat Agmon-Fishman, Cochava Klein, Reut Matar, Lina Basel-Salmon, Idit Maya. Genet Med 2019
31
50

Gene expression differences in Longissimus muscle of Nelore steers genetically divergent for residual feed intake.
Polyana C Tizioto, Luiz L Coutinho, Priscila S N Oliveira, Aline S M Cesar, Wellison J S Diniz, Andressa O Lima, Marina I Rocha, Jared E Decker, Robert D Schnabel, Gerson B Mourão,[...]. Sci Rep 2016
31
50

Ashkenazi Jewish centenarians do not demonstrate enrichment in mitochondrial haplogroup J.
Liran I Shlush, Gil Atzmon, Roni Weisshof, Doron Behar, Guenady Yudkovsky, Nir Barzilai, Karl Skorecki. PLoS One 2008
16
50

Diagnostic and Severity-Tracking Biomarkers for Autism Spectrum Disorder.
Geir Bjørklund, Nagwa A Meguid, Afaf El-Ansary, Mona A El-Bana, Maryam Dadar, Jan Aaseth, Maha Hemimi, Joško Osredkar, Salvatore Chirumbolo. J Mol Neurosci 2018
17
50


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
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
513
50

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
323
50

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
632
50

DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders.
Ganesh J Swaminathan, Eugene Bragin, Eleni A Chatzimichali, Manuel Corpas, A Paul Bevan, Caroline F Wright, Nigel P Carter, Matthew E Hurles, Helen V Firth. Hum Mol Genet 2012
41
50

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
136
50

INTER-ETHNIC MIXTURE AMONG THE COMMUNITIES OF ISRAEL.
E GOLDSCHMIDT, T COHEN. Cold Spring Harb Symp Quant Biol 1964
12
50

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
50

Array CGH in molecular diagnosis of mental retardation - A study of 150 Finnish patients.
Linda Siggberg, Sirpa Ala-Mello, Elisa Jaakkola, Esa Kuusinen, Robert Schuit, Jürgen Kohlhase, Detlef Böhm, Jaakko Ignatius, Sakari Knuutila. Am J Med Genet A 2010
29
50


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
124
50

Genetic causes of intellectual disability in a birth cohort: a population-based study.
Simone M Karam, Mariluce Riegel, Sandra L Segal, Têmis M Félix, Aluísio J D Barros, Iná S Santos, Alicia Matijasevich, Roberto Giugliani, Maureen Black. Am J Med Genet A 2015
16
50


Multiplex ligation-dependent probe amplification to subtelomeric rearrangements in idiopathic intellectual disability in Colombia.
Adalbeis Medina, Lorena Piñeros, Clara Arteaga, Harvy Velasco, Alvaro Izquierdo, Alejandro Giraldo, Eugenia Espinosa. Pediatr Neurol 2014
3
50


Prevalence and characteristics of children with mild intellectual disability in a French county.
M David, K Dieterich, A Billette de Villemeur, P-S Jouk, J Counillon, B Larroque, J Bloch, C Cans. J Intellect Disabil Res 2014
12
50

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
146
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.