A citation-based method for searching scientific literature

Xiuqing Ji, Qiong Pan, Yan Wang, Yun Wu, Jing Zhou, An Liu, Fengchang Qiao, Dingyuan Ma, Ping Hu, Zhengfeng Xu. Front Genet 2018
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
Hong-Dan Wang, Lin Liu, Dong Wu, Tao Li, Cun-Ying Cui, Lian-Zhong Zhang, Cheng-Zeng Wang. J Gene Med 2017
9
100


Can syndromic macrocephaly be diagnosed in utero?
G Malinger, D Lev, L Ben-Sira, C Hoffmann, M Herrera, F Viñals, H Vinkler, S Ginath, Y Biran-Gol, D Kidron,[...]. Ultrasound Obstet Gynecol 2011
5
50

Estimating fetal age: computer-assisted analysis of multiple fetal growth parameters.
F P Hadlock, R L Deter, R B Harrist, S K Park. Radiology 1984
346
50


Fetal sex and intrauterine growth patterns.
Nir Melamed, Israel Meizner, Reuven Mashiach, Arnon Wiznitzer, Marek Glezerman, Yariv Yogev. J Ultrasound Med 2013
32
50

Microcephaly: an epidemiologic analysis.
Melissa J Krauss, Adelaide E Morrissey, Hung N Winn, Erol Amon, Terry L Leet. Am J Obstet Gynecol 2003
42
50

Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
138
50

Microcephaly: general considerations and aids to nosology.
J M Opitz, M C Holt. J Craniofac Genet Dev Biol 1990
66
50

Congenital microcephaly.
Diana Alcantara, Mark O'Driscoll. Am J Med Genet C Semin Med Genet 2014
78
50

Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.
Paranchai Boonsawat, Pascal Joset, Katharina Steindl, Beatrice Oneda, Laura Gogoll, Silvia Azzarello-Burri, Frenny Sheth, Chaitanya Datar, Ishwar C Verma, Ratna Dua Puri,[...]. Genet Med 2019
19
50


Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors.
John C Herriges, Sara Brown, Maria Longhurst, Jillian Ozmore, John B Moeschler, Aura Janze, Jeanne Meck, Sarah T South, Erica F Andersen. Eur J Med Genet 2019
12
50

Genomic and phenotypic delineation of congenital microcephaly.
Ranad Shaheen, Sateesh Maddirevula, Nour Ewida, Saud Alsahli, Ghada M H Abdel-Salam, Maha S Zaki, Saeed Al Tala, Amal Alhashem, Ameen Softah, Mohammed Al-Owain,[...]. Genet Med 2019
32
50

A developmental and genetic classification for malformations of cortical development: update 2012.
A James Barkovich, Renzo Guerrini, Ruben I Kuzniecky, Graeme D Jackson, William B Dobyns. Brain 2012
490
50

Sex-specific antenatal reference growth charts for uncomplicated singleton pregnancies at 15-40 weeks of gestation.
P Schwärzler, J M Bland, D Holden, S Campbell, Y Ville. Ultrasound Obstet Gynecol 2004
79
50

Extending the phenotypic spectrum of RBFOX1 deletions: Sporadic focal epilepsy.
Dennis Lal, Katharina Pernhorst, Karl Martin Klein, Philipp Reif, Rossana Tozzi, Mohammad R Toliat, Georg Winterer, Bernd Neubauer, Peter Nürnberg, Felix Rosenow,[...]. Epilepsia 2015
21
50

Global and regional estimates of preeclampsia and eclampsia: a systematic review.
Edgardo Abalos, Cristina Cuesta, Ana L Grosso, Doris Chou, Lale Say. Eur J Obstet Gynecol Reprod Biol 2013
414
50

PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.
Julián Nevado, Jill A Rosenfeld, Rocío Mena, María Palomares-Bralo, Elena Vallespín, María Ángeles Mori, Jair A Tenorio, Karen W Gripp, Elizabeth Denenberg, Miguel Del Campo,[...]. Eur J Hum Genet 2015
16
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


The phenotype of Sotos syndrome in adulthood: A review of 44 individuals.
Alison Foster, Anna Zachariou, Chey Loveday, Tazeen Ashraf, Edward Blair, Jill Clayton-Smith, Huw Dorkins, Alan Fryer, Blanca Gener, David Goudie,[...]. Am J Med Genet C Semin Med Genet 2019
11
50

The diagnosis of fetal microcephaly.
F A Chervenak, P Jeanty, F Cantraine, U Chitkara, I Venus, R L Berkowitz, J C Hobbins. Am J Obstet Gynecol 1984
137
50

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis.
M I Srebniak, M Joosten, M F C M Knapen, L R Arends, M Polak, S van Veen, A T J I Go, D Van Opstal. Ultrasound Obstet Gynecol 2018
40
50

Sex differences in fetal growth and immediate birth outcomes in a low-risk Caucasian population.
Sander Galjaard, Lieveke Ameye, Christoph C Lees, Anne Pexsters, Tom Bourne, Dirk Timmerman, Roland Devlieger. Biol Sex Differ 2019
12
50


Quantitative phenotypic and network analysis of 1q44 microdeletion for microcephaly.
Nicholas Raun, Janette Mailo, Egidio Spinelli, Xu He, Sarah McAvena, Logan Brand, Julia O'Sullivan, John Andersen, Lawrence Richer, Richard Tang-Wai,[...]. Am J Med Genet A 2017
11
50

Diagnostic approach to microcephaly in childhood: a two-center study and review of the literature.
Maja von der Hagen, Mark Pivarcsi, Juliane Liebe, Horst von Bernuth, Nataliya Didonato, Julia B Hennermann, Christoph Bührer, Dagmar Wieczorek, Angela M Kaindl. Dev Med Child Neurol 2014
96
50


Prenatally diagnosed microcephaly: a review of etiologies.
L Dahlgren, R D Wilson. Fetal Diagn Ther 2001
15
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

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
389
50

Prenatal diagnosis of an atypical 1q21.1 microdeletion and duplication associated with foetal urogenital abnormalities.
Can Liao, Fang Fu, Cui-Xing Yi, Ru Li, Xin Yang, Qin Xu, Dong-Zhi Li. Gene 2012
6
50

Application of array-comparative genomic hybridization in tetralogy of Fallot.
Lin Liu, Hong-Dan Wang, Cun-Ying Cui, Dong Wu, Tao Li, Tai-Bing Fan, Bang-Tian Peng, Lian-Zhong Zhang, Cheng-Zeng Wang. Medicine (Baltimore) 2016
5
50

Expanding the phenotype of reciprocal 1q21.1 deletions and duplications: a case series.
Martina Busè, Helenia C Cuttaia, Daniela Palazzo, Marcella V Mazara, Salvatrice A Lauricella, Michela Malacarne, Mauro Pierluigi, Simona Cavani, Maria Piccione. Ital J Pediatr 2017
15
50

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
50

Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.
Antonio Benítez-Burraco, Montserrat Barcos-Martínez, Isabel Espejo-Portero, Maite Fernández-Urquiza, Raúl Torres-Ruiz, Sandra Rodríguez-Perales, Ma Salud Jiménez-Romero. Front Pediatr 2018
5
50

1q21.1 Microduplication expression in adults.
Alessia Dolcetti, Candice K Silversides, Christian R Marshall, Anath C Lionel, Dimitri J Stavropoulos, Stephen W Scherer, Anne S Bassett. Genet Med 2013
58
50

Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Candice K Silversides, Anath C Lionel, Gregory Costain, Daniele Merico, Ohsuke Migita, Ben Liu, Tracy Yuen, Jessica Rickaby, Bhooma Thiruvahindrapuram, Christian R Marshall,[...]. PLoS Genet 2012
106
50

1q21.1 Duplication syndrome and epilepsy: Case report and review.
Ioulia Gourari, Romaine Schubert, Aparna Prasad. Neurol Genet 2018
5
50


Phenotypic variability and genetic susceptibility to genomic disorders.
Santhosh Girirajan, Evan E Eichler. Hum Mol Genet 2010
185
50

1q21.1 microduplication: large verbal-nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number.
Jean Xavier, Bo Zhou, Frédéric Bilan, Xianglong Zhang, Brigitte Gilbert-Dussardier, Sylvie Viaux-Savelon, Reenal Pattni, Steve S Ho, David Cohen, Douglas F Levinson,[...]. NPJ Genom Med 2018
4
50

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
50

Regulation of human heart contractility by essential myosin light chain isoforms.
M Morano, U Zacharzowski, M Maier, P E Lange, V Alexi-Meskishvili, H Haase, I Morano. J Clin Invest 1996
97
50

New microdeletion and microduplication syndromes: A comprehensive review.
Julián Nevado, Rafaella Mergener, María Palomares-Bralo, Karen Regina Souza, Elena Vallespín, Rocío Mena, Víctor Martínez-Glez, María Ángeles Mori, Fernando Santos, Sixto García-Miñaur,[...]. Genet Mol Biol 2014
54
50


Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients.
Sarah Vergult, A Jeannette M Hoogeboom, Emilia K Bijlsma, Tom Sante, Eva Klopocki, Bram De Wilde, Marjolijn Jongmans, Christian Thiel, Joke B G M Verheij, Antonio Perez-Aytes,[...]. Genet Med 2013
9
50

An estimation of the prevalence of genomic disorders using chromosomal microarray data.
Madelyn A Gillentine, Philip J Lupo, Pawel Stankiewicz, Christian P Schaaf. J Hum Genet 2018
15
50

Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family.
Judith M A Verhagen, Nicole de Leeuw, Dimitri N M Papatsonis, Els W M Grijseels, Ronald R de Krijger, Marja W Wessels. Mol Syndromol 2015
11
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.