A citation-based method for searching scientific literature

Lin Li, Linhuan Huang, Shaobin Lin, Yanmin Luo, Qun Fang. Am J Med Genet A 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma.
Joe Rainger, Kathleen A Williamson, Dinesh C Soares, Julia Truch, Dominic Kurian, Gabriele Gillessen-Kaesbach, Anne Seawright, James Prendergast, Mihail Halachev, Ann Wheeler,[...]. Hum Mutat 2017
12
25

Neural epidermal growth factor-like like protein 2 (NELL2) promotes aggregation of embryonic carcinoma P19 cells by inducing N-cadherin expression.
Dong Hee Kim, Han Rae Kim, Eun Jung Choi, Dong Yeol Kim, Kwang Kon Kim, Byung Sam Kim, Jeong Woo Park, Byung Ju Lee. PLoS One 2014
9
25

CNV biology in neurodevelopmental disorders.
Toru Takumi, Kota Tamada. Curr Opin Neurobiol 2018
39
25

Phenotype-genotype correlation in two patients with 12q proximal deletion.
Noriko Miyake, Hidefumi Tonoki, Marta Gallego, Naoki Harada, Osamu Shimokawa, Koh-ichiro Yoshiura, Tohru Ohta, Tatsuya Kishino, Norio Niikawa, Naomichi Matsumoto. J Hum Genet 2004
15
25

Mutations in ARID2 are associated with intellectual disabilities.
Linshan Shang, Megan T Cho, Kyle Retterer, Leandra Folk, Jennifer Humberson, Luis Rohena, Alpa Sidhu, Sheila Saliganan, Alejandro Iglesias, Patrik Vitazka,[...]. Neurogenetics 2015
29
25


A Role of Central NELL2 in the Regulation of Feeding Behavior in Rats.
Jin Kwon Jeong, Jae Geun Kim, Han Rae Kim, Tae Hwan Lee, Jeong Woo Park, Byung Ju Lee. Mol Cells 2017
3
33

A novel transmembrane protein defines the endoplasmic reticulum stress-induced cell death pathway.
Tomoya Tamaki, Kenta Kamatsuka, Taku Sato, Shuntaro Morooka, Kosuke Otsuka, Masahiro Hattori, Tomoyasu Sugiyama. Biochem Biophys Res Commun 2017
4
25

Haploinsufficiency of ANO6, NELL2 and DBX2 in a boy with intellectual disability and growth delay.
Ellen Ø Carlsen, Eirik Frengen, Madeleine Fannemel, Doriana Misceo. Am J Med Genet A 2015
8
25

Diagnosis and clinical management of duplications and deletions.
Antonio Capalbo, Laura Rienzi, Filippo Maria Ubaldi. Fertil Steril 2017
12
25

A novel deletion of IGF1 in a patient with idiopathic short stature provides insight Into IGF1 haploinsufficiency.
Lara Batey, Jennifer E Moon, Yongguo Yu, Bingbing Wu, Joel N Hirschhorn, Yiping Shen, Andrew Dauber. J Clin Endocrinol Metab 2014
24
25


Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
Chelsea Lowther, Gregory Costain, Danielle A Baribeau, Anne S Bassett. Curr Psychiatry Rep 2017
18
25

12q12 deletion: a new patient contributing to genotype-phenotype correlation.
Pinella Failla, Corrado Romano, Santina Reitano, Daniela Di Benedetto, Lucia Grillo, Marco Fichera, Lucia Castiglia. Am J Med Genet A 2008
8
25

A family with a 1.17 Mb deletion of 12q12: refining genotype-phenotype correlation.
Margaret P Adam, Ami Mehta, Linda Knight, David E Hall, Michael R Rossi. Am J Med Genet A 2010
7
25

Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis.
M Cristina Digilio, Laura Bernardini, Federica Consoli, Francesca R Lepri, M Grazia Giuffrida, Anwar Baban, Cecilia Surace, Rosangela Ferese, Adriano Angioni, Antonio Novelli,[...]. Eur J Med Genet 2013
24
25

Identical but not the same: the value of discordant monozygotic twins in genetic research.
Petra J G Zwijnenburg, Hanne Meijers-Heijboer, Dorret I Boomsma. Am J Med Genet B Neuropsychiatr Genet 2010
70
25

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck,[...]. Genet Med 2019
55
25

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
355
25

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
390
25

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
297
25

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
515
25

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Cornelis A Albers, Dirk S Paul, Harald Schulze, Kathleen Freson, Jonathan C Stephens, Peter A Smethurst, Jennifer D Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone,[...]. Nat Genet 2012
254
25

A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.
Valentina Guida, Rosangela Ferese, Marcella Rocchetti, Monica Bonetti, Anna Sarkozy, Serena Cecchetti, Vania Gelmetti, Francesca Lepri, Massimiliano Copetti, Giuseppe Lamorte,[...]. Eur J Hum Genet 2013
24
25

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen,[...]. Taiwan J Obstet Gynecol 2018
3
33

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
150
25

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Rachel Soemedi, Ana Topf, Ian J Wilson, Rebecca Darlay, Thahira Rahman, Elise Glen, Darroch Hall, Ni Huang, Jamie Bentham, Shoumo Bhattacharya,[...]. Hum Mol Genet 2012
72
25

High incidence of cardiac malformations in connexin40-deficient mice.
Hong Gu, Frank C Smith, Steven M Taffet, Mario Delmar. Circ Res 2003
91
25

Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.
Jill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, Elizabeth W McPherson, Blake C Ballif, Eva Klopocki, Stefan Mundlos, Lisa G Shaffer, Arthur S Aylsworth. Eur J Hum Genet 2012
62
25

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
154
25

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
25

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations.
C Hernando, A Plaja, M A Rigola, M M Pérez, T Vendrell, J Egocue, C Fuster. J Med Genet 2002
31
25

Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis.
Lijuan Sun, Qingqing Wu, Shi-Wen Jiang, Yani Yan, Xin Wang, Juan Zhang, Yan Liu, Ling Yao, Yuqing Ma, Li Wang. Biomed Res Int 2015
25
25

Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study.
C Ferencz, C A Neill, J A Boughman, J D Rubin, J I Brenner, L W Perry. J Pediatr 1989
196
25

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel,[...]. Prenat Diagn 2012
74
25


Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications.
Jill A Rosenfeld, Justine Coppinger, Bassem A Bejjani, Santhosh Girirajan, Evan E Eichler, Lisa G Shaffer, Blake C Ballif. J Neurodev Disord 2010
107
25

Congenital malformations of the central nervous system: clinical approach.
Feriha Hadzagić-Catibusić, Hajrija Maksić, Sajra Uzicanin, Suada Heljić, Smail Zubcević, Zulejha Merhemić, Adisa Cengić, Edina Kulenović. Bosn J Basic Med Sci 2008
14
25

Evaluation of Fetal Central Nervous System Anomalies by Ultrasound and Its Anatomical Co-relation.
Deepali Onkar, Prashant Onkar, Kajal Mitra. J Clin Diagn Res 2014
18
25

Karyotype versus microarray testing for genetic abnormalities after stillbirth.
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
140
25

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
128
25

A new microduplication syndrome encompassing the region of the Miller-Dieker (17p13 deletion) syndrome.
L Roos, A E Jønch, S Kjaergaard, K Taudorf, H Simonsen, B Hamborg-Petersen, K Brøndum-Nielsen, M Kirchhoff. J Med Genet 2009
52
25

Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
Kathleen E Sullivan. Immunol Allergy Clin North Am 2008
60
25

Molecular genetics in fetal neurology.
Jin Huang, Isabella Y M Wah, Ritsuko K Pooh, Kwong Wai Choy. Semin Fetal Neonatal Med 2012
13
25


Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Trilochan Sahoo, Natasa Dzidic, Michelle N Strecker, Sara Commander, Mary K Travis, Charles Doherty, R Weslie Tyson, Arturo E Mendoza, Mary Stephenson, Craig A Dise,[...]. Genet Med 2017
61
25

Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs.
Madita Schumann, Andrea Hofmann, Sophia K Krutzke, Alina C Hilger, Florian Marsch, Dietlinde Stienen, Ulrich Gembruch, Michael Ludwig, Waltraut M Merz, Heiko Reutter. J Neurodev Disord 2016
8
25

Changing clinical presentations and survival pattern in trisomy 18.
Chien-Chou Hsiao, Lon-Yen Tsao, Hsiao-Neng Chen, Han-Yao Chiu, Weng-Cheng Chang. Pediatr Neonatol 2009
24
25

Copy number variations associated with fetal congenital kidney malformations.
Meiying Cai, Na Lin, Linjuan Su, Xiaoqing Wu, Xiaorui Xie, Ying Li, Xuemei Chen, Yuan Lin, Hailong Huang, Liangpu Xu. Mol Cytogenet 2020
2
50

Microarrays in prenatal diagnosis.
Beatrice Oneda, Anita Rauch. Best Pract Res Clin Obstet Gynaecol 2017
20
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.