A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
35
33

De novo 7q36 deletion: breakpoint analysis and types of holoprosencephaly.
S G Frints, E F Schoenmakers, E Smeets, P Petit, J P Fryns. Am J Med Genet 1998
24
33

18p monosomy with midline defects and a de novo satellite identified by FISH.
L Taine, C Goizet, Z Q Wen, J F Chateil, J Battin, R Saura, D Lacombe. Ann Genet 1997
18
33

Expression survey of genes critical for tooth development in the human embryonic tooth germ.
Dahe Lin, Yide Huang, Fenglei He, Shuping Gu, Guozhong Zhang, YiPing Chen, Yanding Zhang. Dev Dyn 2007
42
33

Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
J P Fryns, A Kleczkowska, K Devriendt, H Devliegher, H Van den Berghe. Genet Couns 1993
7
33

Holoprosencephaly: the Maastricht experience.
U Moog, C E De Die-Smulders, C T Schrander-Stumpel, J J Engelen, A J Hamers, S Frints, J P Fryns. Genet Couns 2001
22
33

[Solitary upper incisor, hypopituitarism and monosomy 18p chromosome aberration].
B Boudailliez, N Morichon-Delvallez, A Goldfarb, J C Pautard, C Lenaerts, C Piussan. J Genet Hum 1983
16
33

Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
Sabina Domené, Erich Roessler, Kenia B El-Jaick, Mirit Snir, Jamie L Brown, Jorge I Vélez, Sherri Bale, Felicitas Lacbawan, Maximilian Muenke, Benjamin Feldman. Hum Mol Genet 2008
41
33

Triple-X syndrome accompanied by single maxillary central incisor: case report.
M Miura, N Kato, H Kojima, H Oguchi. Pediatr Dent 1993
13
33

The spectrum of 4q- syndrome illustrated by a case series.
Eugen-Matthias Strehle, Dariusz Gruszfeld, Daniel Schenk, Sarju G Mehta, Ingrid Simonic, Taosheng Huang. Gene 2012
18
33

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
65
33

Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome.
C P Chen, S P Lin, D S Lin, Y P Liu, L J Hsu, W Wang. Genet Couns 2012
3
33

18p - syndrome with a single central maxillary incisor.
L M Dolan, K Willson, W G Wilson. J Med Genet 1981
33
33

Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
Kenichiro Taniguchi, Anoush E Anderson, Ann E Sutherland, David Wotton. PLoS Genet 2012
57
33


Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: association with an 18p11.3 deletion.
Piranit N Kantaputra, Chanin Limwongse, Chintana Tochareontanaphol, Apiwat Mutirangura, Umnat Mevatee, Verayuth Praphanphoj. Am J Med Genet A 2006
16
33


[Mosaic trisomy 9: report of a new case with a long-term survival].
J Sánchez Zahonero, M Andrés Celma, M J López García. An Pediatr (Barc) 2008
2
50

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
33

Single maxillary central incisor in a girl with del(18p) syndrome.
D J Aughton, A A AlSaadi, D J Transue. J Med Genet 1991
37
33

SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.
L Nanni, J E Ming, Y Du, R K Hall, M Aldred, A Bankier, M Muenke. Am J Med Genet 2001
101
33

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
27
33

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
33

DiGeorge syndrome associated with solitary median maxillary central incisor.
Huai-Chih Yang, Shyh-Dar Shyur, Li-Hsin Huang, Yi-Chi Chang, Da-Chin Wen, Pei-Hsuan Liang, Mao-Tsair Lin. Asian Pac J Allergy Immunol 2005
11
33

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
52
33

A new mutation in the six-domain of SIX3 gene causes holoprosencephaly.
L Pasquier, C Dubourg, M Blayau, L Lazaro, B Le Marec, V David, S Odent. Eur J Hum Genet 2000
53
33

A child with 18p- syndrome: a case report.
Antoniella Busuttil Naudi, Diane E Fung. Spec Care Dentist 2007
3
33

Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly.
Ute Hehr, Daniel E Pineda-Alvarez, Goekhan Uyanik, Ping Hu, Nan Zhou, Andreas Hehr, Chayim Schell-Apacik, Carola Altus, Cornelia Daumer-Haas, Annechristin Meiner,[...]. Hum Genet 2010
25
33


A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndrome.
Jan Miertus, Wiktor Borozdin, Vladimir Frecer, Giorgio Tonini, Sara Bertok, Antonio Amoroso, Stanislav Miertus, Jürgen Kohlhase. Hum Genet 2006
24
33


Familial short stature due to a 5q22.1-q23.2 duplication refines the 5q duplication spectrum.
Diana Zahnleiter, Udo Trautmann, Arif B Ekici, Ina Goehring, André Reis, Helmuth-Günther Dörr, Anita Rauch, Christian T Thiel. Eur J Med Genet 2011
5
33

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
32
33

Nasal pyriform aperture stenosis and the holoprosencephaly spectrum.
E Tavin, E Stecker, R Marion. Int J Pediatr Otorhinolaryngol 1994
57
33

Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes.
Deepak Kamnasaran, Chih-Ping Chen, Koenraad Devriendt, Lakshmi Mehta, Diane W Cox. Genomics 2005
31
33

Discordant phenotypes in a mother and daughter with mosaic supernumerary ring chromosome 19 explained by a de novo 7q36.2 deletion and 7p22.1 duplication.
Bob Argiropoulos, Melissa Carter, Kathy Brierley, Heather Hare, Amélie Bouchard, Walla Al-Hertani, Shannon R Ryan, Judith Reid, Mark Basik, Jean McGowan-Jordan,[...]. Am J Med Genet A 2011
5
33

Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
Janneke H M Schuurs-Hoeijmakers, Anneke T Vulto-van Silfhout, Lisenka E L M Vissers, Ilse I G M van de Vondervoort, Bregje W M van Bon, Joep de Ligt, Christian Gilissen, Jayne Y Hehir-Kwa, Kornelia Neveling, Marisol del Rosario,[...]. J Med Genet 2013
59
33

Clinical significance of de novo and inherited copy-number variation.
Anneke T Vulto-van Silfhout, Jayne Y Hehir-Kwa, Bregje W M van Bon, Janneke H M Schuurs-Hoeijmakers, Stephen Meader, Claudia J M Hellebrekers, Ilse J M Thoonen, Arjan P M de Brouwer, Han G Brunner, Caleb Webber,[...]. Hum Mutat 2013
79
33

Partial tandem duplication of GRIA3 in a male with mental retardation.
Tomohiro Chiyonobu, Shin Hayashi, Kazuhiro Kobayashi, Masafumi Morimoto, Yuri Miyanomae, Akira Nishimura, Akemi Nishimoto, Chiyomi Ito, Issei Imoto, Tohru Sugimoto,[...]. Am J Med Genet A 2007
22
33

Support for calcium channel gene defects in autism spectrum disorders.
Ake Tzu-Hui Lu, Xiaoxian Dai, Julian A Martinez-Agosto, Rita M Cantor. Mol Autism 2012
44
33

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
417
33

Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches.
Masashi Ikeda, Yasuyuki Tomita, Akihiro Mouri, Minori Koga, Tomo Okochi, Reiji Yoshimura, Yoshio Yamanouchi, Yoko Kinoshita, Ryota Hashimoto, Hywel J Williams,[...]. Biol Psychiatry 2010
68
33

Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.
Mark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, Jefferson J Doyle, Elena Gallo, Justyna Fert-Bober, Marlies J E Kempers, Elliot K Fishman, Yichun Chen, Loretha Myers,[...]. Nat Genet 2012
269
33


Decreased expression of mineralocorticoid receptor mRNA in the prefrontal cortex in schizophrenia and bipolar disorder.
Guo-Qiang Xing, Shani Russell, Maree J Webster, Robert M Post. Int J Neuropsychopharmacol 2004
57
33

Genetics of early onset cognitive impairment.
Hans Hilger Ropers. Annu Rev Genomics Hum Genet 2010
228
33


Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.
M-L Jacquemont, D Sanlaville, R Redon, O Raoul, V Cormier-Daire, S Lyonnet, J Amiel, M Le Merrer, D Heron, M-C de Blois,[...]. J Med Genet 2006
206
33

Loeys-Dietz syndrome type 4, caused by chromothripsis, involving the TGFB2 gene.
Paolo Fontana, Rita Genesio, Alberto Casertano, Gerarda Cappuccio, Angela Mormile, Lucio Nitsch, Achille Iolascon, Generoso Andria, Daniela Melis. Gene 2014
15
33

A new human MR splice variant is a ligand-independent transactivator modulating corticosteroid action.
M C Zennaro, A Souque, S Viengchareun, E Poisson, M Lombès. Mol Endocrinol 2001
73
33


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.