A citation-based method for searching scientific literature

L Nanni, J E Ming, Y Du, R K Hall, M Aldred, A Bankier, M Muenke. Am J Med Genet 2001
Times Cited: 102







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



Times Cited
  Times     Co-cited
Similarity


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
265
32

Solitary median maxillary central incisor, short stature, choanal atresia/midnasal stenosis (SMMCI) syndrome.
R K Hall, A Bankier, M J Aldred, K Kan, J O Lucas, A G Perks. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1997
54
50

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
859
25

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
304
21

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
20

Solitary median maxillary central incisor syndrome: clinical case with a novel mutation of sonic hedgehog.
Livia Garavelli, C Zanacca, G Caselli, G Banchini, C Dubourg, V David, S Odent, F Gurrieri, G Neri. Am J Med Genet A 2004
30
66


Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation.
Ute Hehr, Claudia Gross, Uta Diebold, Dagmar Wahl, Ulrike Beudt, Peter Heidemann, Andreas Hehr, Dietmar Mueller. Eur J Pediatr 2004
46
36


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
161
15

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
286
15

Previously undescribed nonsense mutation in SHH caused autosomal dominant holoprosencephaly with wide intrafamilial variability.
Monica Marini, Roberto Cusano, Pierangela De Biasio, Francesco Caroli, Margherita Lerone, Margherita Silengo, Roberto Ravazzolo, Marco Seri, Gianni Camera. Am J Med Genet A 2003
27
55

Single median maxillary central incisor: new data and mutation review.
Kênia B El-Jaick, Renata F Fonseca, Miguel A Moreira, Márcia G Ribeiro, Ana M Bolognese, Sânia O Dias, Eliane T Pereira, Eduardo E Castilla, Iêda M Orioli. Birth Defects Res A Clin Mol Teratol 2007
28
53

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, F Vargas, S W Scherer, L C Tsui, M Muenke. Hum Mol Genet 1997
134
14

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
496
14

Two unrelated cases of single maxillary central incisor with 7q terminal deletion.
M Masuno, Y Fukushima, Y Sugio, M Ikeda, Y Kuroki. Jinrui Idengaku Zasshi 1990
36
38

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
Christèle Dubourg, Leïla Lazaro, Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, Marie-Renée Durou, Sylvie Odent, Véronique David. Hum Mutat 2004
116
14

Single maxillary central incisor in a girl with del(18p) syndrome.
D J Aughton, A A AlSaadi, D J Transue. J Med Genet 1991
38
36

Face, palate, and craniofacial morphology in patients with a solitary median maxillary central incisor.
I Kjaer, K B Becktor, J Lisson, C Gormsen, B G Russell. Eur J Orthod 2001
45
31

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
238
13

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
233
13

Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly.
I M Orioli, E E Castilla, J E Ming, J Nazer, M J Burle de Aguiar, J C Llerena, M Muenke. Hum Genet 2001
41
29


Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephaly.
S Odent, T Atti-Bitach, M Blayau, M Mathieu, J Aug, A L Delezo de, J Y Gall, B Le Marec, A Munnich, V David,[...]. Hum Mol Genet 1999
110
11

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
370
11

Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
F Lacbawan, B D Solomon, E Roessler, K El-Jaick, S Domené, J I Vélez, N Zhou, D Hadley, J Z Balog, R Long,[...]. J Med Genet 2009
67
16

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
280
10



Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
17

Solitary maxillary central incisor and congenital nasal pyriform aperture stenosis.
F S Lo, Y J Lee, S P Lin, E Y Shen, J K Huang, K S Lee. Eur J Pediatr 1998
55
18

18p - syndrome with a single central maxillary incisor.
L M Dolan, K Willson, W G Wilson. J Med Genet 1981
34
29

Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
138
9


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
107
9

Congenital nasal pyriform aperture stenosis.
O E Brown, C M Myer, S C Manning. Laryngoscope 1989
135
9

Strong variable clinical presentation in 3 patients with 7q terminal deletion.
S G Frints, C T Schrander-Stumpel, E F Schoenmakers, J J Engelen, A B Reekers, A M Van den Neucker, E Smeets, H Devlieger, J P Fryns. Genet Couns 1998
33
27



Velocardiofacial syndrome with single central incisor.
Snehlata Oberoi, Karin Vargervik. Am J Med Genet A 2005
24
37

Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
139
9

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
133
8

Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia.
Lisa A Schimmenti, June de la Cruz, Richard Alan Lewis, J D Karkera, Glenda S Manligas, Erich Roessler, Maximilian Muenke. Am J Med Genet A 2003
112
8


Solitary maxillary central incisor and short stature.
E B Rappaport, R A Ulstrom, R J Gorlin, A W Lucky, E Colle, J Miser. J Pediatr 1977
72
11


Nasal pyriform aperture stenosis and the holoprosencephaly spectrum.
E Tavin, E Stecker, R Marion. Int J Pediatr Otorhinolaryngol 1994
59
13

Sonic hedgehog regulates growth and morphogenesis of the tooth.
H R Dassule, P Lewis, M Bei, R Maas, A P McMahon. Development 2000
543
8


Solitary maxillary central incisor and normal stature.
R K Wesley, W H Hoffman, J Perrin, J R Delaney. Oral Surg Oral Med Oral Pathol 1978
34
23


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.