R Benawra, H H Mangurten, D R Duffell. J Pediatr 1980
Times Cited: 47
Times Cited: 47
Times Cited
Times Co-cited
Similarity
Otocephaly-midline malformation association.
J H Hersh, R H McChane, E M Rosenberg, W H Powers, C Corrigan, L Pancratz. Am J Med Genet 1989
J H Hersh, R H McChane, E M Rosenberg, W H Powers, C Corrigan, L Pancratz. Am J Med Genet 1989
12
Familial inheritance of mandibular arch malformations affecting three individuals in one family.
O A Rust, J A Bofill, H G Boch, W E Roberts. South Med J 1999
O A Rust, J A Bofill, H G Boch, W E Roberts. South Med J 1999
60
Monozygotic twin aborted fetuses discordant for holoprosencephaly/synotia.
G A Machin, G H Sperber, J Wootliffe. Teratology 1985
G A Machin, G H Sperber, J Wootliffe. Teratology 1985
18
Embryonic origin of holoprosencephaly: interrelationship of the developing brain and face.
K K Sulik, M C Johnston. Scan Electron Microsc 1982
K K Sulik, M C Johnston. Scan Electron Microsc 1982
6
[Two cases of cyclopia].
Y Castel, D Riviere, L Toudic, Y Nouaille, J L'Henoret, H Duparcmeur, J P Leroy, G Balouet. Ann Pediatr (Paris) 1976
Y Castel, D Riviere, L Toudic, Y Nouaille, J L'Henoret, H Duparcmeur, J P Leroy, G Balouet. Ann Pediatr (Paris) 1976
50
Alcohol embryopathy: some facts and speculations about pathogenesis.
F Majewski. Neurobehav Toxicol Teratol 1981
F Majewski. Neurobehav Toxicol Teratol 1981
6
Cyclopia with trisomy D.
E Z Zimmer, M Y Divon, M Halperin, B A Peretz. Eur J Obstet Gynecol Reprod Biol 1982
E Z Zimmer, M Y Divon, M Halperin, B A Peretz. Eur J Obstet Gynecol Reprod Biol 1982
50
Holoprosencephaly: An update on cytogenetic abnormalities.
Claude Bendavid, Valérie Dupé, Lucie Rochard, Isabelle Gicquel, Christèle Dubourg, Véronique David. Am J Med Genet C Semin Med Genet 2010
Claude Bendavid, Valérie Dupé, Lucie Rochard, Isabelle Gicquel, Christèle Dubourg, Véronique David. Am J Med Genet C Semin Med Genet 2010
8
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
6
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
8
Occurrence of cyclopia, myelomeningocele, deafness, and abducens paralysis in siblings.
U Burck, K R Held, H J Kitschke. Am J Med Genet 1982
U Burck, K R Held, H J Kitschke. Am J Med Genet 1982
18
A case of holoprosencephaly and cebocephaly associated to torch infection.
Nizamettin Kilic, Zeynep Yazici. Int J Pediatr Otorhinolaryngol 2005
Nizamettin Kilic, Zeynep Yazici. Int J Pediatr Otorhinolaryngol 2005
42
The dup(3)(p25 leads to pter) syndrome: a case with holoprosencephaly.
N J Martin, B G Steinberg. Am J Med Genet 1983
N J Martin, B G Steinberg. Am J Med Genet 1983
8
Mediobasal prosencephalic defects, including holoprosencephaly and cyclopia, in relation to the development of the human forebrain.
F Müller, R O'Rahilly. Am J Anat 1989
F Müller, R O'Rahilly. Am J Anat 1989
6
Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly.
M Münke. Am J Med Genet 1989
M Münke. Am J Med Genet 1989
6
Chance vs. causality in the association of Down syndrome and holoprosencephaly.
C J Epstein, S Seto, M Golabi. Am J Med Genet 1988
C J Epstein, S Seto, M Golabi. Am J Med Genet 1988
20
16
Synophthalmia and cyclopia: a histopathologic, radiographic, and organogenetic analysis.
E Torczynski, F A Jacobiec, M C Johnston, R L Font, J A Madewell. Doc Ophthalmol 1977
E Torczynski, F A Jacobiec, M C Johnston, R L Font, J A Madewell. Doc Ophthalmol 1977
6
Cyclopia as a result of an unbalanced familial translocation, rcp(7;18)(q34;q21)
R D Smart, J Ross, G Amann, M M Nelson. Am J Med Genet 1986
R D Smart, J Ross, G Amann, M M Nelson. Am J Med Genet 1986
16
An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly.
A O Martin, J C Perrin, W A Muir, E Ruch, I A Schafer. Clin Genet 1977
A O Martin, J C Perrin, W A Muir, E Ruch, I A Schafer. Clin Genet 1977
15
A further case of cyclopia due to unbalanced segregation of a previously reported rcp(1;7)(q32;q34) familial translocation.
A Schinzel. Am J Med Genet 1986
A Schinzel. Am J Med Genet 1986
9
Holoprosencephaly with median cleft lip. Clinical, pathological, and echoencephalographic study.
H Patel, C L Dolman, M A Byrne. Am J Dis Child 1972
H Patel, C L Dolman, M A Byrne. Am J Dis Child 1972
8
The spectrum of the DiGeorge syndrome.
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
6
Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.
V Váradi, L Szabó, Z Papp. J Med Genet 1980
V Váradi, L Szabó, Z Papp. J Med Genet 1980
6
Descriptive neuropathology of chromosomal disorders in man.
F Gullotta, H Rehder, A Gropp. Hum Genet 1981
F Gullotta, H Rehder, A Gropp. Hum Genet 1981
7
Microcephaly in familial holoprosencephaly.
H H Ardinger, J A Bartley. J Craniofac Genet Dev Biol 1988
H H Ardinger, J A Bartley. J Craniofac Genet Dev Biol 1988
16
Interference with gastrulation during the third week of pregnancy as a cause of some facial abnormalities and CNS defects.
W S Webster, A H Lipson, K K Sulik. Am J Med Genet 1988
W S Webster, A H Lipson, K K Sulik. Am J Med Genet 1988
14
Campomelic dysplasia. Further elucidation of a distinct entity.
B D Hall, J W Spranger. Am J Dis Child 1980
B D Hall, J W Spranger. Am J Dis Child 1980
6
Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
I W Lurie, M K Nedzved, G I Lazjuk, I A Kirillova, E D Cherstvoy. Am J Med Genet 1979
I W Lurie, M K Nedzved, G I Lazjuk, I A Kirillova, E D Cherstvoy. Am J Med Genet 1979
8
The syndrome associated with the partial D-monosomy. Case report and review.
D J Orbeli, I W Lurie, J L Goroshenko. Humangenetik 1971
D J Orbeli, I W Lurie, J L Goroshenko. Humangenetik 1971
8
Are 1q plus chromosomes harmless?
R J Gardner, H R McCreanor, M I Parslow, A M Veale. Clin Genet 1974
R J Gardner, H R McCreanor, M I Parslow, A M Veale. Clin Genet 1974
8
The facial features of holoprosencephaly in anencephalic human specimens. I. Historical review and associated malformations.
R J Lemire, M M Cohen, J B Beckwith, V G Kokich, J R Siebert. Teratology 1981
R J Lemire, M M Cohen, J B Beckwith, V G Kokich, J R Siebert. Teratology 1981
6
Absent left hemidiaphragm, arhinencephaly, and cardiac malformations.
N Fitch, H Srolovitz, Y Robitaille, F Guttman. J Med Genet 1978
N Fitch, H Srolovitz, Y Robitaille, F Guttman. J Med Genet 1978
6
Cytogenetic variants in holoprosencephaly. Report of a case and review of the literature.
P M Ming, D M Goodner, T S Park. Am J Dis Child 1976
P M Ming, D M Goodner, T S Park. Am J Dis Child 1976
13
Detecting and treating retinopathy in patients with type I diabetes mellitus. A health policy model.
J C Javitt, J K Canner, R G Frank, D M Steinwachs, A Sommer. Ophthalmology 1990
J C Javitt, J K Canner, R G Frank, D M Steinwachs, A Sommer. Ophthalmology 1990
6
Effects on the fetal rat eye of maternal benomyl exposure and protein malnutrition.
E R Hoogenboom, J F Ransdell, W G Ellis, R J Kavlock, F J Zeman. Curr Eye Res 1991
E R Hoogenboom, J F Ransdell, W G Ellis, R J Kavlock, F J Zeman. Curr Eye Res 1991
13
Automatic detection of diabetic retinopathy using an artificial neural network: a screening tool.
G G Gardner, D Keating, T H Williamson, A T Elliott. Br J Ophthalmol 1996
G G Gardner, D Keating, T H Williamson, A T Elliott. Br J Ophthalmol 1996
6
Cost effectiveness of current approaches to the control of retinopathy in type I diabetics.
J C Javitt, J K Canner, A Sommer. Ophthalmology 1989
J C Javitt, J K Canner, A Sommer. Ophthalmology 1989
6
Cost-effectiveness of alternative methods for diabetic retinopathy screening.
D R Lairson, J A Pugh, A S Kapadia, R J Lorimor, J Jacobson, R Velez. Diabetes Care 1992
D R Lairson, J A Pugh, A S Kapadia, R J Lorimor, J Jacobson, R Velez. Diabetes Care 1992
6
Medical image processing utilizing neural networks trained on a massively parallel computer.
J P Kerr, E B Bartlett. Comput Biol Med 1995
J P Kerr, E B Bartlett. Comput Biol Med 1995
17
Neural network feature detector for real-time video signal processing.
D Naylor, S Jones, D Myers, J Vincent. Int J Neural Syst 1993
D Naylor, S Jones, D Myers, J Vincent. Int J Neural Syst 1993
100
A relative cost-effectiveness analysis of different methods of screening for diabetic retinopathy.
M J Sculpher, M J Buxton, B A Ferguson, J E Humphreys, J F Altman, D J Spiegelhalter, A J Kirby, J S Jacob, H Bacon, S B Dudbridge. Diabet Med 1991
M J Sculpher, M J Buxton, B A Ferguson, J E Humphreys, J F Altman, D J Spiegelhalter, A J Kirby, J S Jacob, H Bacon, S B Dudbridge. Diabet Med 1991
7
Sonographic findings in otocephaly (synotia).
P D Cayea, F R Bieber, M J Ross, A Davidoff, R Osathanondh, T B Jones. J Ultrasound Med 1985
P D Cayea, F R Bieber, M J Ross, A Davidoff, R Osathanondh, T B Jones. J Ultrasound Med 1985
20
Birth defects monitoring in California: a resource for epidemiological research.
L A Croen, G M Shaw, N G Jensvold, J A Harris. Paediatr Perinat Epidemiol 1991
L A Croen, G M Shaw, N G Jensvold, J A Harris. Paediatr Perinat Epidemiol 1991
4
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
4
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.