A citation-based method for searching scientific literature




K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke, S J Elledge. Nat Genet 2000
Times Cited: 300




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

Genetic Overlap between Holoprosencephaly and Kallmann Syndrome.
K Vaaralahti, T Raivio, R Koivu, L Valanne, E-M Laitinen, J Tommiska. Mol Syndromol 2012
12

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

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

Ethmocephaly caused by de novo translocation 18;21--prenatal diagnosis.
Israel Goldstein, Amir Weissman, Ronit Brill-Zamir, Ilana Laevsky, Arie Drugan. Prenat Diagn 2003
1

[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

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

Holoprosencephaly associated with an apparent isolated 2q37.1-->2q37.3 deletion.
N L Lehman, D H Zaleski, W G Sanger, E D Adickes. Am J Med Genet 2001
18

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