A citation-based method for searching scientific literature

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
Times Cited: 45







List of co-cited articles
365 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
37


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
26

Cri du Chat syndrome.
Paola Cerruti Mainardi. Orphanet J Rare Dis 2006
97
26

The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita.
T Vulliamy, A Marrone, F Goldman, A Dearlove, M Bessler, P J Mason, I Dokal. Nature 2001
681
24


Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
Tom Vulliamy, Anna Marrone, Richard Szydlo, Amanda Walne, Philip J Mason, Inderjeet Dokal. Nat Genet 2004
322
22

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
20

[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
17

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
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
19


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
17

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
30

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
15

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
17

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
16


Specific association of human telomerase activity with immortal cells and cancer.
N W Kim, M A Piatyszek, K R Prowse, C B Harley, M D West, P L Ho, G M Coviello, W E Wright, S L Weinrich, J W Shay. Science 1994
15

Telomere shortening and tumor formation by mouse cells lacking telomerase RNA.
M A Blasco, H W Lee, M P Hande, E Samper, P M Lansdorp, R A DePinho, C W Greider. Cell 1997
15

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
N S Heiss, S W Knight, T J Vulliamy, S M Klauck, S Wiemann, P J Mason, A Poustka, I Dokal. Nat Genet 1998
631
13

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
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
40

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
27

Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA.
Patrick F Fogarty, Hiroki Yamaguchi, Adrian Wiestner, Gabriela M Baerlocher, Elaine Sloand, Weihua S Zeng, Elizabeth J Read, Peter M Lansdorp, Neal S Young. Lancet 2003
190
13

Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome.
Hiroki Yamaguchi, Gabriela M Baerlocher, Peter M Lansdorp, Stephen J Chanock, Olga Nunez, Elaine Sloand, Neal S Young. Blood 2003
215
13

Association between aplastic anaemia and mutations in telomerase RNA.
Tom Vulliamy, Anna Marrone, Inderjeet Dokal, Philip J Mason. Lancet 2002
211
13

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
24

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
13

Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia.
Hiroki Yamaguchi, Rodrigo T Calado, Hinh Ly, Sachiko Kajigaya, Gabriela M Baerlocher, Stephen J Chanock, Peter M Lansdorp, Neal S Young. N Engl J Med 2005
485
13

Preferential maintenance of critically short telomeres in mammalian cells heterozygous for mTert.
Yie Liu, Hue Kha, Mark Ungrin, Murray O Robinson, Lea Harrington. Proc Natl Acad Sci U S A 2002
84
11

Haploinsufficiency of mTR results in defects in telomere elongation.
Karen S Hathcock, Michael T Hemann, Kay Keyer Opperman, Margaret A Strong, Carol W Greider, Richard J Hodes. Proc Natl Acad Sci U S A 2002
87
11


Mouse dyskerin mutations affect accumulation of telomerase RNA and small nucleolar RNA, telomerase activity, and ribosomal RNA processing.
Yuko Mochizuki, Jun He, Shashikant Kulkarni, Monica Bessler, Philip J Mason. Proc Natl Acad Sci U S A 2004
134
11

The telomerase reverse transcriptase is limiting and necessary for telomerase function in vivo.
Y Liu, B E Snow, M P Hande, D Yeung, N J Erdmann, A Wakeham, A Itie, D P Siderovski, P M Lansdorp, M O Robinson,[...]. Curr Biol 2000
183
11

Longevity, stress response, and cancer in aging telomerase-deficient mice.
K L Rudolph, S Chang, H W Lee, M Blasco, G J Gottlieb, C Greider, R A DePinho. Cell 1999
986
11


Essential role of mouse telomerase in highly proliferative organs.
H W Lee, M A Blasco, G J Gottlieb, J W Horner, C W Greider, R A DePinho. Nature 1998
999
11

Telomerase catalytic subunit homologs from fission yeast and human.
T M Nakamura, G B Morin, K B Chapman, S L Weinrich, W H Andrews, J Lingner, C B Harley, T R Cech. Science 1997
11

Telomeres shorten during ageing of human fibroblasts.
C B Harley, A B Futcher, C W Greider. Nature 1990
11

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
11

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
11

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
29

Systematic analysis of telomere length and somatic alterations in 31 cancer types.
Floris P Barthel, Wei Wei, Ming Tang, Emmanuel Martinez-Ledesma, Xin Hu, Samirkumar B Amin, Kadir C Akdemir, Sahil Seth, Xingzhi Song, Qianghu Wang,[...]. Nat Genet 2017
222
11

Telomerase maintains telomere structure in normal human cells.
Kenkichi Masutomi, Evan Y Yu, Shilagardy Khurts, Ittai Ben-Porath, Jennifer L Currier, Geoffrey B Metz, Mary W Brooks, Shuichi Kaneko, Seishi Murakami, James A DeCaprio,[...]. Cell 2003
576
8

Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice.
S E Artandi, S Chang, S L Lee, S Alson, G J Gottlieb, L Chin, R A DePinho. Nature 2000
838
8


Antenatal sonographic features of cri-du-chat syndrome.
S Aoki, T Hata, K Hata, K Miyazaki. Ultrasound Obstet Gynecol 1999
16
25

Frequent amplification of the telomerase reverse transcriptase gene in human tumors.
A Zhang, C Zheng, C Lindvall, M Hou, J Ekedahl, R Lewensohn, Z Yan, X Yang, M Henriksson, E Blennow,[...]. Cancer Res 2000
118
8



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.