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Times Cited: 225
Times Cited: 225
Times Cited
Times Co-cited
Similarity
THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY).
W DEMYER, W ZEMAN, C G PALMER. Pediatrics 1964
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Holoprosencephaly in human embryos: epidemiologic studies of 150 cases.
E Matsunaga, K Shiota. Teratology 1977
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Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities.
M M Cohen. Am J Med Genet 1989
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L A Croen, G M Shaw, E J Lammer. Am J Med Genet 1996
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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
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M M Cohen. Teratology 1989
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Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
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Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
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Holoprosencephaly in infants of diabetic mothers.
M Barr, J W Hanson, K Currey, S Sharp, H Toriello, R D Schmickel, G N Wilson. J Pediatr 1983
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Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989.
C L Olsen, J P Hughes, L G Youngblood, M Sharpe-Stimac. Am J Med Genet 1997
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Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies.
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The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
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Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
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Holoprosencephaly: birth data, benetic and demographic analyses of 30 families.
E Roach, W Demyer, P M Conneally, C Palmer, A D Merritt. Birth Defects Orig Artic Ser 1975
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Holoprosencephaly: a paradigm for the complex genetics of brain development.
E Roessler, M Muenke. J Inherit Metab Dis 1998
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Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
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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
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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
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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
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Towards a greater understanding of the pathogenesis of holoprosencephaly.
J A Golden. Brain Dev 1999
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Assessment of the deep gray nuclei in holoprosencephaly.
E M Simon, R Hevner, J D Pinter, N J Clegg, V S Miller, S L Kinsman, J S Hahn, A J Barkovich. AJNR Am J Neuroradiol 2000
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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
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Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.
Jeffrey E Ming, Maximilian Muenke. Am J Hum Genet 2002
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Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?
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Pathoarchitectonic studies of cerebral malformations. III. Arrhinencephalies (holotelencephalies).
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Investigation of the epidemiology and prenatal diagnosis of holoprosencephaly in the North of England.
P J Bullen, J M Rankin, S C Robson. Am J Obstet Gynecol 2001
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Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain.
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M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
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Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
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Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.
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Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.
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Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation.
Jin S Hahn, Patrick D Barnes. Am J Med Genet C Semin Med Genet 2010
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Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
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Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.
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Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
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Risk factors for cytogenetically normal holoprosencephaly in California: a population-based case-control study.
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Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.
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Evaluation and management of children with holoprosencephaly.
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Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases.
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Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
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Physical mapping of the holoprosencephaly critical region on chromosome 7q36.
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Segregation analysis in nonsyndromic holoprosencephaly.
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A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
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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.