A citation-based method for searching scientific literature

Fei Chen, Haiming Yuan, Wenyong Wu, Shaoke Chen, Qi Yang, Jin Wang, Qiang Zhang, Baohen Gui, Xin Fan, Ruimin Chen, Yiping Shen. Am J Med Genet C Semin Med Genet 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


De novo mutations in the genome organizer CTCF cause intellectual disability.
Anne Gregor, Martin Oti, Evelyn N Kouwenhoven, Juliane Hoyer, Heinrich Sticht, Arif B Ekici, Susanne Kjaergaard, Anita Rauch, Hendrik G Stunnenberg, Steffen Uebe,[...]. Am J Hum Genet 2013
82
57

Identification of a novel CTCF mutation responsible for syndromic intellectual disability - a case report.
Fatma Bastaki, Pratibha Nair, Madiha Mohamed, Ethar Mustafa Malik, Mustafa Helmi, Mahmoud Taleb Al-Ali, Abdul Rezzak Hamzeh. BMC Med Genet 2017
19
57

CTCF deletion syndrome: clinical features and epigenetic delineation.
Ikumi Hori, Rie Kawamura, Kazuhiko Nakabayashi, Hidetaka Watanabe, Ken Higashimoto, Junko Tomikawa, Daisuke Ieda, Kei Ohashi, Yutaka Negishi, Ayako Hattori,[...]. J Med Genet 2017
11
42

CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum.
Enrico D H Konrad, Niels Nardini, Almuth Caliebe, Inga Nagel, Dana Young, Gabriella Horvath, Stephanie L Santoro, Christine Shuss, Alban Ziegler, Dominique Bonneau,[...]. Genet Med 2019
11
42

Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
Linyan Meng, Mohan Pammi, Anirudh Saronwala, Pilar Magoulas, Andrew Ray Ghazi, Francesco Vetrini, Jing Zhang, Weimin He, Avinash V Dharmadhikari, Chunjing Qu,[...]. JAMA Pediatr 2017
174
28

CTCF, a conserved nuclear factor required for optimal transcriptional activity of the chicken c-myc gene, is an 11-Zn-finger protein differentially expressed in multiple forms.
E M Klenova, R H Nicolas, H F Paterson, A F Carne, C M Heath, G H Goodwin, P E Neiman, V V Lobanenkov. Mol Cell Biol 1993
213
28

CTCF is required for neural development and stochastic expression of clustered Pcdh genes in neurons.
Teruyoshi Hirayama, Etsuko Tarusawa, Yumiko Yoshimura, Niels Galjart, Takeshi Yagi. Cell Rep 2012
106
28

De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
A Jeremy Willsey, Thomas V Fernandez, Dongmei Yu, Robert A King, Andrea Dietrich, Jinchuan Xing, Stephan J Sanders, Jeffrey D Mandell, Alden Y Huang, Petra Richer,[...]. Neuron 2017
67
28

Dual effect of CTCF loss on neuroprogenitor differentiation and survival.
L Ashley Watson, Xu Wang, Adrienne Elbert, Kristin D Kernohan, Niels Galjart, Nathalie G Bérubé. J Neurosci 2014
39
28


Clinical application of whole-exome sequencing across clinical indications.
Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan,[...]. Genet Med 2016
433
28

ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
815
28

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.
Sarah B Ng, Abigail W Bigham, Kati J Buckingham, Mark C Hannibal, Margaret J McMillin, Heidi I Gildersleeve, Anita E Beck, Holly K Tabor, Gregory M Cooper, Heather C Mefford,[...]. Nat Genet 2010
832
28

Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome.
Nancy Mizue Kokitsu-Nakata, Aline Lourenço Petrin, Jason Paul Heard, Siulan Vendramini-Pittoli, Laura E Henkle, Daniela Vera Cruz dos Santos, Jeffrey Clark Murray, Antonio Richieri-Costa. Am J Med Genet A 2012
15
28

Training in clinical genetics and genetic counseling in Asia.
Eva Maria Cutiongco-de la Paz, Brian Hon-Yin Chung, Sultana M H Faradz, Meow-Keong Thong, Carmencita David-Padilla, Poh San Lai, Shuan-Pei Lin, Yin-Hsiu Chen, Thanyachai Sura, Mercy Laurino. Am J Med Genet C Semin Med Genet 2019
2
50

Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
304
14

The different facets of "culture" in genetic counseling: A situated analysis of genetic counseling in Hong Kong.
Olga Zayts, Hannah Shipman, Jasmine L-F Fung, Anthony P-Y Liu, Sit-Yee Kwok, Anne C-H Tsai, Tak-Cheung Yung, Brian H-Y Chung. Am J Med Genet C Semin Med Genet 2019
1
100

Genetic studies on systemic lupus erythematosus in East Asia point to population differences in disease susceptibility.
Yong-Fei Wang, Yu Lung Lau, Wanling Yang. Am J Med Genet C Semin Med Genet 2019
5
20

Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia.
Pornswan Wasant, Carmencita Padilla, Stephen Lam, Meow-Keong Thong, Poh-San Lai. Am J Med Genet C Semin Med Genet 2019
1
100


Precision medicine in Thailand.
Vorasuk Shotelersuk, Sissades Tongsima, Manop Pithukpakorn, Jakris Eu-Ahsunthornwattana, Surakameth Mahasirimongkol. Am J Med Genet C Semin Med Genet 2019
7
14

Genetic landscape of RASopathies in Chinese: Three decades' experience in Hong Kong.
Kris P T Yu, Ho-Ming Luk, Gordon K C Leung, Christopher C Y Mak, Shirley S W Cheng, Edgar W L Hau, David K H Chan, Stephen T S Lam, Tony M F Tong, Brian H Y Chung,[...]. Am J Med Genet C Semin Med Genet 2019
3
33

The rise of the genetic counseling profession in China.
Liya Sun, Bo Liang, Liping Zhu, Yiping Shen, Lin He. Am J Med Genet C Semin Med Genet 2019
7
14

A review of aromatic l-amino acid decarboxylase (AADC) deficiency in Taiwan.
Ni-Chung Lee, Yin-Hsiu Chien, Wuh-Liang Hwu. Am J Med Genet C Semin Med Genet 2019
4
25

Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.
Shirley S W Cheng, Kelvin Y K Chan, Kelphen K P Leung, Patrick K C Au, Wai-Keung Tam, Samuel K M Li, Ho-Ming Luk, Anita S Y Kan, Brian H Y Chung, Ivan F M Lo,[...]. Am J Med Genet C Semin Med Genet 2019
12
14

Mutational spectrum of dystrophinopathies in Singapore: Insights for genetic diagnosis and precision therapy.
Swati Tomar, Vikaesh Moorthy, Raman Sethi, Josiah Chai, Poh Sim Low, Stacey Tay Kiat Hong, Poh San Lai. Am J Med Genet C Semin Med Genet 2019
6
16

Noonan syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Yonit A Addissie, Angélica Moresco, Sofia Medrano, Gary T K Mok, Gordon K C Leung, Cedrik Tekendo-Ngongang, Annette Uwineza, Meow-Keong Thong,[...]. Am J Med Genet A 2017
40
14

Medical genetics and genomic medicine in Japan.
Hisato Suzuki, Tomoko Watanabe, Tomoko Uehara, Kenjiro Kosaki. Am J Med Genet C Semin Med Genet 2019
3
33

STAR: ultrafast universal RNA-seq aligner.
Alexander Dobin, Carrie A Davis, Felix Schlesinger, Jorg Drenkow, Chris Zaleski, Sonali Jha, Philippe Batut, Mark Chaisson, Thomas R Gingeras. Bioinformatics 2013
14

Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila.
Jonas Straub, Enrico D H Konrad, Johanna Grüner, Annick Toutain, Levinus A Bok, Megan T Cho, Heather P Crawford, Holly Dubbs, Ganka Douglas, Rebekah Jobling,[...]. Am J Hum Genet 2018
27
14

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
14

CTCF is conserved from Drosophila to humans and confers enhancer blocking of the Fab-8 insulator.
Hanlim Moon, Galina Filippova, Dmitry Loukinov, Elena Pugacheva, Qi Chen, Sheryl T Smith, Adam Munhall, Britta Grewe, Marek Bartkuhn, Rüdiger Arnold,[...]. EMBO Rep 2005
182
14




3D Chromosome Regulatory Landscape of Human Pluripotent Cells.
Xiong Ji, Daniel B Dadon, Benjamin E Powell, Zi Peng Fan, Diego Borges-Rivera, Sigal Shachar, Abraham S Weintraub, Denes Hnisz, Gianluca Pegoraro, Tong Ihn Lee,[...]. Cell Stem Cell 2016
206
14

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Nara Sobreira, François Schiettecatte, David Valle, Ada Hamosh. Hum Mutat 2015
589
14

A versatile platform for creating a comprehensive UAS-ORFeome library in Drosophila.
Johannes Bischof, Mikael Björklund, Edy Furger, Claus Schertel, Jussi Taipale, Konrad Basler. Development 2013
152
14


Modifications of seizure susceptibility in Drosophila.
D Kuebler, M A Tanouye. J Neurophysiol 2000
79
14

CTCF, a candidate trans-acting factor for X-inactivation choice.
Wendy Chao, Khanh D Huynh, Rebecca J Spencer, Lance S Davidow, Jeannie T Lee. Science 2002
207
14



A chromatin insulator determines the nuclear localization of DNA.
T I Gerasimova, K Byrd, V G Corces. Mol Cell 2000
260
14

Loss of maternal CTCF is associated with peri-implantation lethality of Ctcf null embryos.
James M Moore, Natalia A Rabaia, Leslie E Smith, Sara Fagerlie, Kay Gurley, Dmitry Loukinov, Christine M Disteche, Steven J Collins, Christopher J Kemp, Victor V Lobanenkov,[...]. PLoS One 2012
57
14

Conditioned responses in courtship behavior of normal and mutant Drosophila.
R W Siegel, J C Hall. Proc Natl Acad Sci U S A 1979
299
14

PANTHER version 11: expanded annotation data from Gene Ontology and Reactome pathways, and data analysis tool enhancements.
Huaiyu Mi, Xiaosong Huang, Anushya Muruganujan, Haiming Tang, Caitlin Mills, Diane Kang, Paul D Thomas. Nucleic Acids Res 2017
14

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.
Michael I Love, Wolfgang Huber, Simon Anders. Genome Biol 2014
14

Nature and function of insulator protein binding sites in the Drosophila genome.
Yuri B Schwartz, Daniela Linder-Basso, Peter V Kharchenko, Michael Y Tolstorukov, Maria Kim, Hua-Bing Li, Andrey A Gorchakov, Aki Minoda, Gregory Shanower, Artyom A Alekseyenko,[...]. Genome Res 2012
121
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.