A citation-based method for searching scientific literature


List of co-cited articles
510 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Diagnosis and management of fetal holoprosencephaly.
F A Chervenak, G Isaacson, J C Hobbins, U Chitkara, M Tortora, R L Berkowitz. Obstet Gynecol 1985
52
7

Dorsal third ventricular cyst: an entity distinct from holoprosencephaly.
J N Young, W J Oakes, H P Hatten. J Neurosurg 1992
18
22


Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly--a new syndrome? Part I: clinical, causal, and pathogenetic considerations.
J G Hall, P D Pallister, S K Clarren, J B Beckwith, F W Wiglesworth, F C Fraser, S Cho, P J Benke, S D Reed. Am J Med Genet 1980
236
4

Holoprosencephaly: prenatal sonographic diagnosis.
D A Nyberg, L A Mack, A Bronstein, J Hirsch, R A Pagon. AJR Am J Roentgenol 1987
48
8

Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz syndrome.
G S Tint, M Irons, E R Elias, A K Batta, R Frieden, T S Chen, G Salen. N Engl J Med 1994
626
4

Prenatal diagnosis of lobar holoprosencephaly.
G Pilu, F Sandri, A Perolo, F Giangaspero, G Cocchi, G P Salvioli, L Bovicelli. Ultrasound Obstet Gynecol 1992
15
26


Midline signalling is required for Pax gene regulation and patterning of the eyes.
R Macdonald, K A Barth, Q Xu, N Holder, I Mikkola, S W Wilson. Development 1995
358
4


Median lip clefts of the upper lip.
D R Millard, S Williams. Plast Reconstr Surg 1968
59
6



Unusual variant of holoprosencephaly in monosomy 13q.
Pascale Marcorelles, Philippe Loget, Catherine Fallet-Bianco, Joëlle Roume, Ferechte Encha-Razavi, Anne-Lise Delezoide. Pediatr Dev Pathol 2002
22
18

9
44

How a Hedgehog might see holoprosencephaly.
Erich Roessler, Maximilian Muenke. Hum Mol Genet 2003
51
7

Median cleft of the lip: its significance and surgical repair.
J Apesos, G M Anigian. Cleft Palate Craniofac J 1993
27
14

Hedgehog signaling is required for pituitary gland development.
M Treier, S O'Connell, A Gleiberman, J Price, D P Szeto, R Burgess, P T Chuang, A P McMahon, M G Rosenfeld. Development 2001
208
4

Neuropathologic research strategies in holoprosencephaly.
H B Sarnat, L Flores-Sarnat. J Child Neurol 2001
60
6



The Carter Neurocognitive Assessment for children with severely compromised expressive language and motor skills.
Hilary J Leevers, Cynthia P Roesler, Judy Flax, April A Benasich. J Child Psychol Psychiatry 2005
10
40

Cerebral midline developmental anomalies: spectrum and associated features.
A L Delezoide, F Narcy, J C Larroche. Genet Couns 1990
12
33


Holoprosencephaly.
D M Peebles. Prenat Diagn 1998
36
11

Prenatal MR findings of the middle interhemispheric variant of holoprosencephaly.
Steven B Pulitzer, Erin M Simon, Timothy M Crombleholme, Jeffrey A Golden. AJNR Am J Neuroradiol 2004
25
16

Differential diagnosis in fetuses with absent septum pellucidum.
G Malinger, D Lev, D Kidron, F Heredia, R Hershkovitz, T Lerman-Sagie. Ultrasound Obstet Gynecol 2005
63
6

Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.
Erich Roessler, Yong Ma, Maia V Ouspenskaia, Felicitas Lacbawan, Claude Bendavid, Christèle Dubourg, Philip A Beachy, Maximilian Muenke. Hum Genet 2009
50
8

Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
Erich Roessler, Maia V Ouspenskaia, Jayaprakash D Karkera, Jorge I Vélez, Amy Kantipong, Felicitas Lacbawan, Peter Bowers, John W Belmont, Jeffrey A Towbin, Elizabeth Goldmuntz,[...]. Am J Hum Genet 2008
101
4

What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
10

Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother.
M Urioste, E Valcarcel, M A Gomez, I Pinel, R Garcia de León, A Diaz de Bustamante, R Tebar, M L Martinez-Frias. Am J Med Genet 1988
29
13

Disorders of prosencephalic development.
P Volpe, G Campobasso, V De Robertis, G Rembouskos. Prenat Diagn 2009
49
8

Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.
Claude Bendavid, Lucie Rochard, Christèle Dubourg, Jonathan Seguin, Isabelle Gicquel, Laurent Pasquier, Jaqueline Vigneron, Annie Laquerrière, Pascale Marcorelles, Corinne Jeanne-Pasquier,[...]. Hum Mutat 2009
35
11

Pathogenesis of holoprosencephaly.
Xin Geng, Guillermo Oliver. J Clin Invest 2009
59
6

Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients.
Daniel E Pineda-Alvarez, Christèle Dubourg, Véronique David, Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
46
8

New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, Boris Campillo-Gimenez, Isabelle Gicquel, Marion Belleguic, Leslie Ratié, Laurent Pasquier, Philippe Loget, Claude Bendavid,[...]. J Med Genet 2011
76
5


Holoprosencephaly and related entities.
C R Fitz. Neuroradiology 1983
62
4


Gli1 is a target of Sonic hedgehog that induces ventral neural tube development.
J Lee, K A Platt, P Censullo, A Ruiz i Altaba. Development 1997
473
3


Determination of the zebrafish forebrain: induction and patterning.
Y Grinblat, J Gamse, M Patel, H Sive. Development 1998
107
3

Six3 overexpression initiates the formation of ectopic retina.
F Loosli, S Winkler, J Wittbrodt. Genes Dev 1999
182
3

Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome.
B U Fitzky, M Witsch-Baumgartner, M Erdel, J N Lee, Y K Paik, H Glossmann, G Utermann, F F Moebius. Proc Natl Acad Sci U S A 1998
296
3


GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.
S Kang, J M Graham, A H Olney, L G Biesecker. Nat Genet 1997
358
3

Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction.
A Glinka, W Wu, H Delius, A P Monaghan, C Blumenstock, C Niehrs. Nature 1998
3

Control of cell pattern in the neural tube by the zinc finger transcription factor and oncogene Gli-1.
M Hynes, D M Stone, M Dowd, S Pitts-Meek, A Goddard, A Gurney, A Rosenthal. Neuron 1997
227
3

The Shh signalling pathway in tooth development: defects in Gli2 and Gli3 mutants.
Z Hardcastle, R Mo, C C Hui, P T Sharpe. Development 1998
272
3



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.