A citation-based method for searching scientific literature

L Y Brown, S Odent, V David, M Blayau, C Dubourg, C Apacik, M A Delgado, B D Hall, J F Reynolds, A Sommer, D Wieczorek, S A Brown, M Muenke. Hum Mol Genet 2001
Times Cited: 138







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



Times Cited
  Times     Co-cited
Similarity


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
49

Zic2 regulates the kinetics of neurulation.
T Nagai, J Aruga, O Minowa, T Sugimoto, Y Ohno, T Noda, K Mikoshiba. Proc Natl Acad Sci U S A 2000
179
37

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
843
30

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
283
25

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
301
25

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
259
23


The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation.
T Nagai, J Aruga, S Takada, T Günther, R Spörle, K Schughart, K Mikoshiba. Dev Biol 1997
267
20

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
18

Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
110
18

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
17

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
17

Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.
Nicholas Warr, Nicola Powles-Glover, Anna Chappell, Joan Robson, Dominic Norris, Ruth M Arkell. Hum Mol Genet 2008
68
25

Physical and functional interactions between Zic and Gli proteins.
Y Koyabu, K Nakata, K Mizugishi, J Aruga, K Mikoshiba. J Biol Chem 2001
148
15

Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly.
I M Orioli, E E Castilla, J E Ming, J Nazer, M J Burle de Aguiar, J C Llerena, M Muenke. Hum Genet 2001
41
36


The middle interhemispheric variant of holoprosencephaly.
Erin M Simon, Robert F Hevner, Joseph D Pinter, Nancy J Clegg, Mauricio Delgado, Stephen L Kinsman, Jin S Hahn, A James Barkovich. AJNR Am J Neuroradiol 2002
96
15

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.
B Brais, J P Bouchard, Y G Xie, D L Rochefort, N Chrétien, F M Tomé, R G Lafrenière, J M Rommens, E Uyama, O Nohira,[...]. Nat Genet 1998
559
14


Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
159
14

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
237
14

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
487
14

Central roles of the roof plate in telencephalic development and holoprosencephaly.
Xun Cheng, Ching-mei Hsu, D Spencer Currle, Jia Sheng Hu, A James Barkovich, Edwin S Monuki. J Neurosci 2006
80
17

The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
Erich Roessler, Felicitas Lacbawan, Christèle Dubourg, Aimee Paulussen, Jos Herbergs, Ute Hehr, Claude Bendavid, Nan Zhou, Maia Ouspenskaia, Sherri Bale,[...]. Hum Mutat 2009
49
28

Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency.
Frédéric Laumonnier, Nathalie Ronce, Ben C J Hamel, Paul Thomas, James Lespinasse, Martine Raynaud, Christine Paringaux, Hans Van Bokhoven, Vera Kalscheuer, Jean-Pierre Fryns,[...]. Am J Hum Genet 2002
205
13

Zic2 is required for neural crest formation and hindbrain patterning during mouse development.
Paul Elms, Pam Siggers, Diane Napper, Andy Greenfield, Ruth Arkell. Dev Biol 2003
82
15

Overlapping and distinct expression domains of Zic2 and Zic3 during mouse gastrulation.
Paul Elms, Andrew Scurry, Jennifer Davies, Catherine Willoughby, Terry Hacker, Debora Bogani, Ruth Arkell. Gene Expr Patterns 2004
50
26

Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
139
13

Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Benjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, Nancy J Clegg, Mauricio R Delgado, Kenneth Rosenbaum, Christèle Dubourg, Veronique David, Ann Haskins Olney, Lars-Erik Wehner,[...]. J Med Genet 2010
57
22

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
S Mundlos, F Otto, C Mundlos, J B Mulliken, A S Aylsworth, S Albright, D Lindhout, W G Cole, W Henn, J H Knoll,[...]. Cell 1997
12

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.
Petter Strømme, Marie E Mangelsdorf, Marie A Shaw, Karen M Lower, Suzanne M E Lewis, Helene Bruyere, Viggo Lütcherath, Agi K Gedeon, Robyn H Wallace, Ingrid E Scheffer,[...]. Nat Genet 2002
322
12

The role of Zic genes in neural development.
Jun Aruga. Mol Cell Neurosci 2004
188
12

The mouse zic gene family. Homologues of the Drosophila pair-rule gene odd-paired.
J Aruga, T Nagai, T Tokuyama, Y Hayashizaki, Y Okazaki, V M Chapman, K Mikoshiba. J Biol Chem 1996
170
12


Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
12

Possible association of NTDs with a polyhistidine tract polymorphism in the ZIC2 gene.
Lúcia Y Brown, Susan E Hodge, William G Johnson, Sandra G Guy, Jeffrey S Nye, Stephen Brown. Am J Med Genet 2002
26
42

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.
Jeanne Amiel, Béatrice Laudier, Tania Attié-Bitach, Ha Trang, Loïc de Pontual, Blanca Gener, Delphine Trochet, Heather Etchevers, Pierre Ray, Michel Simonneau,[...]. Nat Genet 2003
558
11

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
80
13

Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.
A J Lewis, E M Simon, A J Barkovich, N J Clegg, M R Delgado, E Levey, J S Hahn. Neurology 2002
64
17


Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
199
11

The ZIC gene family in development and disease.
I Grinberg, K J Millen. Clin Genet 2005
107
11

Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.
F R Goodman, C Bacchelli, A F Brady, L A Brueton, J P Fryns, D P Mortlock, J W Innis, L B Holmes, A E Donnenfeld, M Feingold,[...]. Am J Hum Genet 2000
165
10

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
10


Zic1 promotes the expansion of dorsal neural progenitors in spinal cord by inhibiting neuronal differentiation.
Jun Aruga, Takahide Tohmonda, Shunsaku Homma, Katsuhiko Mikoshiba. Dev Biol 2002
103
10

Zic2 controls cerebellar development in cooperation with Zic1.
Jun Aruga, Takashi Inoue, Jun Hoshino, Katsuhiko Mikoshiba. J Neurosci 2002
103
10

Mouse Zic5 deficiency results in neural tube defects and hypoplasia of cephalic neural crest derivatives.
Takashi Inoue, Minoru Hatayama, Takahide Tohmonda, Shigeyoshi Itohara, Jun Aruga, Katsuhiko Mikoshiba. Dev Biol 2004
76
13




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.