A citation-based method for searching scientific literature




M Barr, J W Hanson, K Currey, S Sharp, H Toriello, R D Schmickel, G N Wilson. J Pediatr 1983
Times Cited: 158




List of shared articles



Times cited

Disorders of Ventral Induction/Spectrum of Holoprosencephaly.
Sonia Francesca Calloni, Luca Caschera, Fabio Maria Triulzi. Neuroimaging Clin N Am 2019
2

Rare Disease: Lobar Holoprosencephaly With a Median Cleft Lip-Case Report.
Julija Radojicic, Tatjana Tanic, Zoran Pesic, Nebojsa Jovic, Tatjana Cutovic, Gordana Filipovic. Cleft Palate Craniofac J 2016
1

Holoprosencephaly: antenatal and postnatal diagnosis and outcome.
Chandrasekaran Kaliaperumal, Sam Ndoro, Tafadzwa Mandiwanza, F Reidy, F McAuliffe, John Caird, Darach Crimmins. Childs Nerv Syst 2016
8

Ethmocephaly: A rare cephalic disorder.
Pooja Dewan, Smriti Rohatgi, Shambhawi Roy, Prerna Batra. J Pediatr Neurosci 2016
1

Cyclopia: a rare condition with unusual presentation - a case report.
Ghassan Sa Salama, Mahmoud Af Kaabneh, Mohamed K Al-Raqad, Ibrahim Mh Al-Abdallah, Ayoub Ga Shakkoury, Ruba Aa Halaseh. Clin Med Insights Pediatr 2015
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

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

Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects.
Jennifer F Dennis, Hiroshi Kurosaka, Angelo Iulianella, Jennifer Pace, Nancy Thomas, Sharon Beckham, Trevor Williams, Paul A Trainor. PLoS Genet 2012
40


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

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


[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

Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases.
H G K Blaas, A G Eriksson, K A Salvesen, C V Isaksen, B Christensen, G Møllerløkken, S H Eik-Nes. Ultrasound Obstet Gynecol 2002
63

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

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



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

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

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