A citation-based method for searching scientific literature




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
Times Cited: 158




List of shared articles



Times cited

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

Risk factors for nonsyndromic holoprosencephaly: a Manitoba case-control study.
Simone S Vaz, Bernard Chodirker, Chitra Prasad, Jamie A Seabrook, Albert E Chudley, Asuri N Prasad. Am J Med Genet A 2012
10

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

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

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


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: genetic, neuroradiological, and clinical advances.
Jin S Hahn, Joseph D Pinter. Semin Pediatr Neurol 2002
6