A citation-based method for searching scientific literature

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
Times Cited: 38







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



Times Cited
  Times     Co-cited
Similarity


Cri du Chat syndrome.
Paola Cerruti Mainardi. Orphanet J Rare Dis 2006
99
52


Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation.
P C Mainardi, C Perfumo, A Calì, G Coucourde, G Pastore, S Cavani, F Zara, J Overhauser, M Pierluigi, F D Bricarelli. J Med Genet 2001
105
42

High-resolution mapping of genotype-phenotype relationships in cri du chat syndrome using array comparative genomic hybridization.
Xiaoxiao Zhang, Antoine Snijders, Richard Segraves, Xiuqing Zhang, Anita Niebuhr, Donna Albertson, Huanming Yang, Joe Gray, Erik Niebuhr, Lars Bolund,[...]. Am J Hum Genet 2005
96
26


The natural history of Cri du Chat Syndrome. A report from the Italian Register.
Paola Cerruti Mainardi, Guido Pastore, Chiara Castronovo, Michela Godi, Andrea Guala, Stefania Tamiazzo, Sandro Provera, Mauro Pierluigi, Franca Dagna Bricarelli. Eur J Med Genet 2006
44
23

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
61

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
47


[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
J LEJEUNE, J LAFOURCADE, R BERGER, J VIALATTE, M BOESWILLWALD, P SERINGE, R TURPIN. C R Hebd Seances Acad Sci 1963
322
18

Cri-Du-Chat Syndrome: Clinical Profile and Chromosomal Microarray Analysis in Six Patients.
Layla Damasceno Espirito Santo, Lília Maria Azevedo Moreira, Mariluce Riegel. Biomed Res Int 2016
10
70

Genotype-phenotype correlation of 5p-syndrome: pitfall of diagnosis.
Tatsuro Kondoh, Osamu Shimokawa, Naoki Harada, Tomoki Doi, Chyuns Yun, Yuji Gohda, Fumiko Kinoshita, Tadashi Matsumoto, Hiroyuki Moriuchi. J Hum Genet 2005
18
38

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndrome.
J Overhauser, X Huang, M Gersh, W Wilson, J McMahon, U Bengtsson, K Rojas, M Meyer, J J Wasmuth. Hum Mol Genet 1994
128
15

Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.
Chih-Ping Chen, Chen-Chi Lee, Tung-Yao Chang, Dai-Dyi Town, Wayseen Wang. Prenat Diagn 2004
22
22

Livebirth prevalence and follow-up of malformation syndromes in 27,472 newborns.
M Higurashi, M Oda, K Iijima, S Iijima, T Takeshita, N Watanabe, K Yoneyama. Brain Dev 1990
68
13


Prenatal diagnosis of cri-du-chat syndrome: importance of ultrasonographical markers.
X H Teoh, T Y Tan, K K Chow, I W Lee. Singapore Med J 2009
16
31

Prenatal diagnosis of 5p deletion syndrome: Report of five cases.
Annisa S L Mak, Teresa W L Ma, Kelvin Y K Chan, Anita S Y Kan, Mary H Y Tang, Kwok Y Leung. J Obstet Gynaecol Res 2019
7
71

Integrated analysis of the critical region 5p15.3-p15.2 associated with cri-du-chat syndrome.
Thiago Corrêa, Bruno César Feltes, Mariluce Riegel. Genet Mol Biol 2019
9
55

A familial Cri-du-Chat/5p deletion syndrome resulted from rare maternal complex chromosomal rearrangements (CCRs) and/or possible chromosome 5p chromothripsis.
Heng Gu, Jian-hui Jiang, Jian-ying Li, Ya-nan Zhang, Xing-sheng Dong, Yang-yu Huang, Xin-ming Son, Xinyan Lu, Zheng Chen. PLoS One 2013
23
17

Deletion of the telomerase reverse transcriptase gene and haploinsufficiency of telomere maintenance in Cri du chat syndrome.
Anju Zhang, Chengyun Zheng, Mi Hou, Charlotta Lindvall, Ke-Jun Li, Fredrik Erlandsson, Magnus Björkholm, Astrid Gruber, Elisabeth Blennow, Dawei Xu. Am J Hum Genet 2003
46
10

Five novel genes from the cri-du-chat critical region isolated by direct selection.
A D Simmons, S A Goodart, T D Gallardo, J Overhauser, M Lovett. Hum Mol Genet 1995
42
10

The first three mosaic cri du chat syndrome patients with two rearranged cell lines.
C Perfumo, P Cerruti Mainardi, A Calí, G Coucourde, F Zara, S Cavani, J Overhauser, F D Bricarelli, M Pierluigi. J Med Genet 2000
23
17

Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate interval.
A D Simmons, A W Püschel, J D McPherson, J Overhauser, M Lovett. Biochem Biophys Res Commun 1998
42
7

Cri du chat syndrome: a critical review.
Angela Rodríguez-Caballero, Daniel Torres-Lagares, Antonio Rodríguez-Pérez, María-Angeles Serrera-Figallo, José-María Hernández-Guisado, Guillermo Machuca-Portillo. Med Oral Patol Oral Cir Bucal 2010
20
15

Multigenerational autosomal dominant inheritance of 5p chromosomal deletions.
Bin Zhang, Marcia Willing, Dorothy K Grange, Marwan Shinawi, Linda Manwaring, Marisa Vineyard, Shashikant Kulkarni, Catherine E Cottrell. Am J Med Genet A 2016
9
33


Cri du chat syndrome: changing phenotype in older patients.
G J Van Buggenhout, E Pijkels, M Holvoet, C Schaap, B C Hamel, J P Fryns. Am J Med Genet 2000
42
7


Dandy-Walker syndrome and corpus callosum agenesis in 5p deletion.
F Vialard, R Robyr, Y Hillion, D Molina Gomes, J Selva, Y Ville. Prenat Diagn 2005
19
15

Parental origin of chromosome 5 deletions in the cri-du-chat syndrome.
J Overhauser, J McMahon, S Oberlender, M E Carlin, E Niebuhr, J J Wasmuth, J Lee-Chen. Am J Med Genet 1990
47
7

Prenatal diagnosis of cri du chat syndrome with encephalocele.
Jamie N Bakkum, William J Watson, Keith L Johansen, Brian C Brost. Am J Perinatol 2005
8
37

Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis.
M M Gil, V Accurti, B Santacruz, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2017
261
7

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
7


Evidence for a distinct region causing a cat-like cry in patients with 5p deletions.
M Gersh, S A Goodart, L M Pasztor, D J Harris, L Weiss, J Overhauser. Am J Hum Genet 1995
71
7

No relationship between the size of the deletion and the level of developmental delay in cri-du-chat syndrome.
R C Marinescu, E I Johnson, E M Dykens, R M Hodapp, J Overhauser. Am J Med Genet 1999
15
20

Brain stem hypoplasia associated with Cri-du-Chat syndrome.
Jin Ho Hong, Ha Young Lee, Myung Kwan Lim, Mi Young Kim, Young Hye Kang, Kyung Hee Lee, Soon Gu Cho. Korean J Radiol 2013
6
50

Prenatal sonographic diagnosis of isolated fetal ascites in cri-du-chat (5p-) syndrome: A case report.
Mariana C Cardoso, Maria Inês Raposo, Mariana Ormonde, Rita Monteiro, André Sampaio, Pedro Cosme, Luisa Mota-Vieira. J Clin Ultrasound 2019
3
100

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
7

Cri du Chat syndrome: Characteristics of 73 Brazilian patients.
R S Honjo, C B Mello, L S E Pimenta, E C Nuñes-Vaca, L M Benedetto, R B F Khoury, D M Befi-Lopes, C A Kim. J Intellect Disabil Res 2018
4
75

1p36 deletion syndrome: an update.
Valerie K Jordan, Hitisha P Zaveri, Daryl A Scott. Appl Clin Genet 2015
74
5

The clinical significance of small copy number variants in neurodevelopmental disorders.
Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger,[...]. J Med Genet 2014
57
5

Mosaic cri-du-chat syndrome in a girl with a mild phenotype.
Lilia Maria de Azevedo Moreira, Acácia Fernandes Lacerda de Carvalho, Ana Lúcia Vieira de Freitas Borja, Paula Sanders Pereira Pinto, Adriana Silveira, Lucy Magalhães de Freitas, Maria de Lourdes Lima Falcão. J Appl Genet 2008
5
40

Delta-catenin regulates spine and synapse morphogenesis and function in hippocampal neurons during development.
Jyothi Arikkath, I-Feng Peng, Yu Gie Ng, Inbal Israely, Xin Liu, Erik M Ullian, Louis F Reichardt. J Neurosci 2009
58
5

Psychomotor development in Cri du Chat Syndrome.
P Cerruti Mainardi, A Guala, G Pastore, G Pozzo, F Dagna Bricarelli, M Pierluigi. Clin Genet 2000
10
20

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
180
5

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
5

Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterization.
Maja Hempel, Nuria Rivera Brugués, Janine Wagenstaller, Gaby Lederer, Andrea Weitensteiner, Heide Seidel, Thomas Meitinger, Tim M Strom. Am J Med Genet A 2009
24
8

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
66


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.