A citation-based method for searching scientific literature




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, R A Martin, P Meinecke, M E Pierpont, N H Robin, I D Young, E Roessler, M Muenke. Hum Mol Genet 1999
Times Cited: 258




List of shared articles



Times cited

Rare nasal cleft in a patient with holoprosencephaly due to a mutation in the ZIC2 gene.
Clarice Pagani Savastano, Pricila Bernardi, Hector N Seuánez, Miguel Ângelo Martins Moreira, Iêda Maria Orioli. Birth Defects Res A Clin Mol Teratol 2014
5

Molecular analysis of holoprosencephaly in South America.
Clarice Pagani Savastano, Kênia Balbi El-Jaick, Marcelo Aguiar Costa-Lima, Cristina Maria Batista Abath, Sebastiano Bianca, Denise Pontes Cavalcanti, Têmis Maria Félix, Gioacchino Scarano, Juan Clinton Llerena, Fernando Regla Vargas,[...]. Genet Mol Biol 2014
6

Alobar holoprosencephaly with cyclopia - autopsy-based observations from one medical center.
Jarosław Swatek, Justyna Szumiło, Franciszek Burdan. Reprod Toxicol 2013
2

Holoprosencephaly: a guide to diagnosis and clinical management.
Manu S Raam, Benjamin D Solomon, Maximilian Muenke. Indian Pediatr 2011
22

Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE.
Jill A Rosenfeld, Blake C Ballif, Donna M Martin, Arthur S Aylsworth, Bassem A Bejjani, Beth S Torchia, Lisa G Shaffer. Hum Genet 2010
49

The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.
Aimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, Matteus K M Spee, Alexander P A Stegmann, Grazia M Mancini, Alice S Brooks, Margriet Collée, Anneke Maat-Kievit, Marleen E H Simon,[...]. Eur J Hum Genet 2010
32


Lobar holoprosencephaly with a median cleft: case report.
Elzbieta Gawrych, Joanna Janiszewska-Olszowska, Anna Walecka, Maria Syryńska, Hanna Chojnacka. Cleft Palate Craniofac J 2009
7

Agnathia and associated malformations in a male rhesus monkey.
B Goldschmidt, C A Lopes, M Moura, D M Fasano, M C R Andrade, L B Cysne, M B Gonçalves, J S Bravin, T Kugelmeier, C F Viana,[...]. J Med Primatol 2008
1

Holoprosencephaly.
Jin S Hahn. Handb Clin Neurol 2008
2

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
221

Embryonic holoprosencephaly: pathology and phenotypic variability.
Shigehito Yamada. Congenit Anom (Kyoto) 2006
9

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

Phenotypic variability in human embryonic holoprosencephaly in the Kyoto Collection.
Shigehito Yamada, Chigako Uwabe, Shingo Fujii, Kohei Shiota. Birth Defects Res A Clin Mol Teratol 2004
63


Semilobar holoprosencephaly with midline 'seam': a topologic and morphogenetic model based upon MRI analysis.
T Takahashi, S Kinsman, N Makris, E Grant, C Haselgrove, S McInerney, D N Kennedy, Ta Takahashi, K Fredrickson, S Mori,[...]. Cereb Cortex 2003
18

[Genetic study of holoprosencephaly].
C Dubourg, L Lazaro, M Blayau, L Pasquier, M-R Durou, S Odent, V David. Ann Biol Clin (Paris) 2003
5

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
137

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

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

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