A citation-based method for searching scientific literature

C Dubourg, L Lazaro, M Blayau, L Pasquier, M-R Durou, S Odent, V David. Ann Biol Clin (Paris) 2003
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
L Y Brown, S Odent, V David, M Blayau, C Dubourg, C Apacik, M A Delgado, B D Hall, J F Reynolds, A Sommer,[...]. Hum Mol Genet 2001
138
40

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
365
40

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
Christèle Dubourg, Leïla Lazaro, Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, Marie-Renée Durou, Sylvie Odent, Véronique David. Hum Mutat 2004
115
40

Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
137
40

Segregation analysis in nonsyndromic holoprosencephaly.
S Odent, B Le Marec, A Munnich, M Le Merrer, C Bonaïti-Pellié. Am J Med Genet 1998
43
40


[Lethal polymalformative syndrome with 13q deletion secondary to a maternal X; 13 translocation].
G Vittu, M F Croquette, A Donney, F R Duminy, J Couturier, J Cousin. J Genet Hum 1989
9
20

High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes.
I Chudoba, A Plesch, T Lörch, J Lemke, U Claussen, G Senger. Cytogenet Cell Genet 1999
166
20



The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32.
S Brown, J Russo, D Chitayat, D Warburton. Am J Hum Genet 1995
146
20

Molecular mechanisms of holoprosencephaly.
D E Wallis, M Muenke. Mol Genet Metab 1999
99
20


Recombinant chromosome 13 with a duplication of a short arm. Repository identification No. GM-1570.
M Seabright, N Gregson, M M Aronson, A E Greene, L L Coriell. Cytogenet Cell Genet 1979
3
33

An integrated mBAND and submegabase resolution tiling set (SMRT) CGH array analysis of focal amplification, microdeletions, and ladder structures consistent with breakage-fusion-bridge cycle events in osteosarcoma.
Gloria Lim, Jana Karaskova, Ben Beheshti, Bisera Vukovic, Jane Bayani, Shamini Selvarajah, Spencer K Watson, Wan L Lam, Maria Zielenska, Jeremy A Squire. Genes Chromosomes Cancer 2005
44
20



Purkinje cell inclusions and 'atelencephaly' in 13q-chromosomal syndrome.
J Towfighi, R L Ladda, F E Sharkey. Arch Pathol Lab Med 1987
28
20

Dicentric chromosome 13 and centromere inactivation.
S Schwartz, C G Palmer, D D Weaver, J Priest. Hum Genet 1983
27
20

When, where and how the bridge breaks: anaphase bridge breakage plays a crucial role in gene amplification and HSR generation.
Noriaki Shimizu, Kenta Shingaki, Yukiko Kaneko-Sasaguri, Toshihiko Hashizume, Teru Kanda. Exp Cell Res 2005
114
20

High frequency of centromere inactivation resulting in stable dicentric chromosomes of maize.
Fangpu Han, Jonathan C Lamb, James A Birchler. Proc Natl Acad Sci U S A 2006
181
20


13q- syndrome. Family study.
A Carmichael, D P Addy, W R Shortland-Webb, A H Cameron, I C Davies. Arch Dis Child 1977
15
20


Molecular genetics of holoprosencephaly.
L Nanni, R L Schelper, M T Muenke. Front Biosci 2000
24
20

Interstitial deletion of long arm of chromosome 13.
A Carnevale, S Frias, R Alcantar. Ann Genet 1984
15
20

The 13q-deletion syndrome.
P W Allderdice, J G Davis, O J Miller, H P Klinger, D Warburton, D A Miller, F H Allen, C A Abrams, E McGilvray. Am J Hum Genet 1969
155
20



Partial monosomy and partial trisomy for different segments of chromosome 13 in several individuals of the same family.
R S Wilroy, R L Summitt, P Martens, W M Gooch, C Hood, W Wiser. Birth Defects Orig Artic Ser 1976
4
25

Segregation of digital number with partial monosomy or trisomy of 13q in familial 5;13 translocation.
M Rodríguez de Alba, R Sanz, I Lorda-Sanchez, J M Fernández-Moya, C Ayuso, J Díaz-Recasens, C Ramos. Prenat Diagn 1999
12
20

Identification of MYCN Copy Number Heterogeneity by Direct FISH Analysis of Neuroblastoma Preparations.
Squire, Thorner, Marrano, Parkinson, Ng, Gerrie, Chilton-Macneill, Zielenska. Mol Diagn 1996
25
20

Penoscrotal transposition: a case report and review.
J MacKenzie, D Chitayat, G McLorie, J W Balfe, P B Pandit, S R Blecher. Am J Med Genet 1994
15
20

Peno-scrotal transposition and the caudal regression syndrome.
R R Turnock, R J Brereton. Eur J Pediatr Surg 1991
5
20


The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats.
Aikaterini Barbouti, Pawel Stankiewicz, Chad Nusbaum, Christina Cuomo, April Cook, Mattias Höglund, Bertil Johansson, Anne Hagemeijer, Sung-Sup Park, Felix Mitelman,[...]. Am J Hum Genet 2004
92
20

Double mosaic aneuploidy: 45,X/47,XY,+8 in a male infant.
B Schofield, A Babu, D Punales-Morejon, S Popescu, E Leiter, B Franklin, V B Penchaszadeh. Am J Med Genet 1992
15
20



Holoprosencephaly: from Homer to Hedgehog.
J E Ming, M Muenke. Clin Genet 1998
98
20

Small molecule modulation of Smoothened activity.
James K Chen, Jussi Taipale, Keith E Young, Tapan Maiti, Philip A Beachy. Proc Natl Acad Sci U S A 2002
745
20

Holoprosencephaly: a family showing dominant inheritance and variable expression.
A L Collins, P W Lunt, C Garrett, N R Dennis. J Med Genet 1993
25
20

Inhibition of Hedgehog signaling by direct binding of cyclopamine to Smoothened.
James K Chen, Jussi Taipale, Michael K Cooper, Philip A Beachy. Genes Dev 2002
20


Holoprosencephaly in a bovine calf.
D Y Cho, D H Zeman, J E Miller. Acta Neuropathol 1985
9
20

Early eye development in vertebrates.
R L Chow, R A Lang. Annu Rev Cell Dev Biol 2001
443
20






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.