W DEMYER, W ZEMAN. Confin Neurol 1963
Times Cited: 226
Times Cited: 226
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
W DEMYER, W ZEMAN, C G PALMER. Pediatrics 1964
59
Holoprosencephaly in human embryos: epidemiologic studies of 150 cases.
E Matsunaga, K Shiota. Teratology 1977
E Matsunaga, K Shiota. Teratology 1977
36
Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities.
M M Cohen. Am J Med Genet 1989
M M Cohen. Am J Med Genet 1989
30
Holoprosencephaly: epidemiologic and clinical characteristics of a California population.
L A Croen, G M Shaw, E J Lammer. Am J Med Genet 1996
L A Croen, G M Shaw, E J Lammer. Am J Med Genet 1996
28
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
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
28
Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology.
M M Cohen. Teratology 1989
M M Cohen. Teratology 1989
28
Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
26
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
24
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
M Barr, J W Hanson, K Currey, S Sharp, H Toriello, R D Schmickel, G N Wilson. J Pediatr 1983
24
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
C L Olsen, J P Hughes, L G Youngblood, M Sharpe-Stimac. Am J Med Genet 1997
23
The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
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,[...]. Hum Mol Genet 1999
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,[...]. Hum Mol Genet 1999
21
Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies.
M M Cohen, K K Sulik. J Craniofac Genet Dev Biol 1992
M M Cohen, K K Sulik. J Craniofac Genet Dev Biol 1992
21
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
20
Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
20
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
E Roach, W Demyer, P M Conneally, C Palmer, A D Merritt. Birth Defects Orig Artic Ser 1975
19
Holoprosencephaly: a paradigm for the complex genetics of brain development.
E Roessler, M Muenke. J Inherit Metab Dis 1998
E Roessler, M Muenke. J Inherit Metab Dis 1998
18
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
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
16
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
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
16
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
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
16
Towards a greater understanding of the pathogenesis of holoprosencephaly.
J A Golden. Brain Dev 1999
J A Golden. Brain Dev 1999
20
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
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
24
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
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
16
Multiple hits during early embryonic development: digenic diseases and holoprosencephaly.
Jeffrey E Ming, Maximilian Muenke. Am J Hum Genet 2002
Jeffrey E Ming, Maximilian Muenke. Am J Hum Genet 2002
15
Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
23
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
P J Bullen, J M Rankin, S C Robson. Am J Obstet Gynecol 2001
23
Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain.
L L Plawner, M R Delgado, V S Miller, E B Levey, S L Kinsman, A J Barkovich, E M Simon, N J Clegg, V T Sweet, E E Stashinko,[...]. Neurology 2002
L L Plawner, M R Delgado, V S Miller, E B Levey, S L Kinsman, A J Barkovich, E M Simon, N J Clegg, V T Sweet, E E Stashinko,[...]. Neurology 2002
21
Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
14
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
Jin S Hahn, Patrick D Barnes. Am J Med Genet C Semin Med Genet 2010
14
Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?
R L Kelley, E Roessler, R C Hennekam, G L Feldman, K Kosaki, M C Jones, J C Palumbos, M Muenke. Am J Med Genet 1996
R L Kelley, E Roessler, R C Hennekam, G L Feldman, K Kosaki, M C Jones, J C Palumbos, M Muenke. Am J Med Genet 1996
13
Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
M L Whiteford, J L Tolmie. J Med Genet 1996
32
13
Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.
A J Lewis, E M Simon, A J Barkovich, N J Clegg, M R Delgado, E Levey, J S Hahn. Neurology 2002
A J Lewis, E M Simon, A J Barkovich, N J Clegg, M R Delgado, E Levey, J S Hahn. Neurology 2002
19
Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.
M Muenke, F Gurrieri, C Bay, D H Yi, A L Collins, V P Johnson, R C Hennekam, G B Schaefer, L Weik, M S Lubinsky. Proc Natl Acad Sci U S A 1994
M Muenke, F Gurrieri, C Bay, D H Yi, A L Collins, V P Johnson, R C Hennekam, G B Schaefer, L Weik, M S Lubinsky. Proc Natl Acad Sci U S A 1994
12
Pathoarchitectonic studies of cerebral malformations. III. Arrhinencephalies (holotelencephalies).
P I YAKOVLEV. J Neuropathol Exp Neurol 1959
P I YAKOVLEV. J Neuropathol Exp Neurol 1959
12
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
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
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
12
16
Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.
S A Rasmussen, C A Moore, M J Khoury, J F Cordero. Am J Med Genet 1996
S A Rasmussen, C A Moore, M J Khoury, J F Cordero. Am J Med Genet 1996
26
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
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
11
Risk factors for cytogenetically normal holoprosencephaly in California: a population-based case-control study.
L A Croen, G M Shaw, E J Lammer. Am J Med Genet 2000
L A Croen, G M Shaw, E J Lammer. Am J Med Genet 2000
18
Arhinencephaly. The spectrum of associated malformations.
J A Kobori, M K Herrick, H Urich. Brain 1987
J A Kobori, M K Herrick, H Urich. Brain 1987
25
Evaluation and management of children with holoprosencephaly.
Jin S Hahn, Lauren L Plawner. Pediatr Neurol 2004
Jin S Hahn, Lauren L Plawner. Pediatr Neurol 2004
20
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
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
15
Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
27
Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.
K K Sulik, D B Dehart, J M Rogers, N Chernoff. Teratology 1995
K K Sulik, D B Dehart, J M Rogers, N Chernoff. Teratology 1995
9
Segregation analysis in nonsyndromic holoprosencephaly.
S Odent, B Le Marec, A Munnich, M Le Merrer, C Bonaïti-Pellié. Am J Med Genet 1998
S Odent, B Le Marec, A Munnich, M Le Merrer, C Bonaïti-Pellié. Am J Med Genet 1998
20
A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
11
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
Erich Roessler, Yang-Zhu Du, Jose L Mullor, Esther Casas, William P Allen, Gabriele Gillessen-Kaesbach, Elizabeth R Roeder, Jeffrey E Ming, Ariel Ruiz i Altaba, Maximilian Muenke. Proc Natl Acad Sci U S A 2003
9
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.