A citation-based method for searching scientific literature

Qingfa Wu, Erik Niebuhr, Huanming Yang, Lars Hansen. Eur J Hum Genet 2005
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity



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
43

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
41


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
35

Cri du Chat syndrome.
Paola Cerruti Mainardi. Orphanet J Rare Dis 2006
97
35


[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
323
30

Cognitive functioning in children with typical cri du chat (5p-) syndrome.
K M Cornish, D Bramble, F Munir, J Pigram. Dev Med Child Neurol 1999
34
35

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
28



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
25

Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features.
D M Church, U Bengtsson, K V Nielsen, J J Wasmuth, E Niebuhr. Am J Hum Genet 1995
74
23

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
41
23



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
50

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
52

5p deletions: Current knowledge and future directions.
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
38
23

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
20

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
45
20

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
20

A neuropsychological-genetic profile of atypical cri du chat syndrome: implications for prognosis.
K M Cornish, G Cross, A Green, L Willatt, J M Bradshaw. J Med Genet 1999
25
28

A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5p.
D M Church, J Yang, M Bocian, R Shiang, J J Wasmuth. Genome Res 1997
37
18


Cri du Chat: report of a case.
S Sparks, B Hutchinson. J Commun Disord 1980
11
63

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

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
15

Clinical heterogeneity in 80 home-reared children with cri du chat syndrome.
L E Wilkins, J A Brown, W E Nance, B Wolf. J Pediatr 1983
60
15

8.5 Mb deletion at distal 5p in a male ascertained for azoospermia.
Elena Rossi, Manuela de Gregori, Maria Grazia Patricelli, Tiziano Pramparo, Luisa Argentiero, Sabrina Giglio, Katiuscia Sosta, Giovanni Foresti, Orsetta Zuffardi. Am J Med Genet A 2005
8
75

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
60

Speech and language development in cri du chat syndrome: a critical review.
Kristian Emil Kristoffersen. Clin Linguist Phon 2008
12
50

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
22
27

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
21

Terminal deletion of the short arm of chromosome 5.
C Baccichetti, E Lenzini, L Artifoni, D Caufin, P Marangoni. Clin Genet 1988
31
16


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
33

Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.
Izabela Laczmanska, Agnieszka Stembalska, Justyna Gil, Halina Czemarmazowicz, Maria Sasiadek. Eur J Med Genet 2006
9
55

Growth charts for cri-du-chat syndrome: an international collaborative study.
R C Marinescu, P C Mainardi, M R Collins, M Kouahou, G Coucourde, G Pastore, J Eaton-Evans, J Overhauser. Am J Med Genet 2000
18
22

Consonants in Cri du chat syndrome: a case study.
Kristian Emil Kristoffersen. J Commun Disord 2008
8
50

Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome.
Fernando Jose Martinez, Jeong Ho Lee, Ji Eun Lee, Sandra Blanco, Elizabeth Nickerson, Stacey Gabriel, Michaela Frye, Lihadh Al-Gazali, Joseph G Gleeson. J Med Genet 2012
130
10

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
10



FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome.
R C Marinescu, E I Johnson, D Grady, X N Chen, J Overhauser. Clin Genet 1999
15
20

Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype.
J Overhauser, M S Golbus, S A Schonberg, J J Wasmuth. Am J Hum Genet 1986
113
7


Cri-du-chat syndrome: clinical profile and prenatal diagnosis.
M S Tullu, M N Muranjan, S V Sharma, D R Sahu, S R Swami, C T Deshmukh, B A Bharucha. J Postgrad Med 1998
13
23

Familial 5p- syndrome.
T Kushnick, K W Rao, A N Lamb. Clin Genet 1984
20
15


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.