A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity




A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
H Vastardis, N Karimbux, S W Guthua, J G Seidman, C E Seidman. Nat Genet 1996
506
56


Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.
P Nieminen, S Arte, S Pirinen, L Peltonen, I Thesleff. Hum Genet 1995
79
52


Dominant inheritance of tooth malpositions and their association to hypodontia.
E Svinhufvud, S Myllärniemi, R Norio. Clin Genet 1988
68
48

Gene defect in hypodontia: exclusion of EGF, EGFR, and FGF-3 as candidate genes.
S Arte, P Nieminen, S Pirinen, I Thesleff, L Peltonen. J Dent Res 1996
63
48


MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.
M J van den Boogaard, M Dorland, F A Beemer, H K van Amstel. Nat Genet 2000
418
44


A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.
W Ahmad, V Brancolini, M F ul Faiyaz, H Lam, S ul Haque, M Haider, A Maimon, V M Aita, J Owen, D Brown,[...]. Am J Hum Genet 1998
53
44


X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.
R Döffinger, A Smahi, C Bessia, F Geissmann, J Feinberg, A Durandy, C Bodemer, S Kenwrick, S Dupuis-Girod, S Blanche,[...]. Nat Genet 2001
591
44

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.
N Galili, H S Baldwin, J Lund, R Reeves, W Gong, Z Wang, B A Roe, B S Emanuel, S Nayak, C Mickanin,[...]. Genome Res 1997
73
40

Nager acrofacial dysostosis.
M T McDonald, J L Gorski. J Med Genet 1993
50
40

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
833
40

CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.
G Zhou, Y Chen, L Zhou, K Thirunavukkarasu, J Hecht, D Chitayat, B D Gelb, S Pirinen, S A Berry, C R Greenberg,[...]. Hum Mol Genet 1999
173
40



Perception of breast cancer risk among women in breast center and primary care settings: correlation with age and family history of breast cancer.
B L Smith, M A Gadd, C Lawler, D J MacDonald, S C Grudberg, F S Chi, K Carlson, A Comegno, W W Souba. Surgery 1996
65
40


Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.
P M Kelley, D J Harris, B C Comer, J W Askew, T Fowler, S D Smith, W J Kimberling. Am J Hum Genet 1998
385
40

Congenital macular colobomas and short-limb skeletal dysplasia.
R D Smith, R M Fineman, D O Sillence, P D Lester, G W Nixon, D L Rimoin, R S Lachman. Am J Med Genet 1980
15
66

Detection of single-nucleotide polymorphisms with the WAVE DNA fragment analysis system.
A Kuklin, K Munson, D Gjerde, R Haefele, P Taylor. Genet Test 1997
131
40

Associated malformations and chromosomal defects in congenital diaphragmatic hernia.
R Bollmann, K Kalache, H Mau, R Chaoui, C Tennstedt. Fetal Diagn Ther 1995
81
40

Associated anomalies in individuals with polydactyly.
E E Castilla, R Lugarinho, M da Graça Dutra, L J Salgado. Am J Med Genet 1998
47
40

A simple salting out procedure for extracting DNA from human nucleated cells.
S A Miller, D D Dykes, H F Polesky. Nucleic Acids Res 1988
40



Structural chromosome anomalies in congenital diaphragmatic hernia.
D T Howe, M D Kilby, H Sirry, G M Barker, E Roberts, E V Davison, J Mchugo, M J Whittle. Prenat Diagn 1996
74
40


[Incidence of familial defective apolipoprotein B-100 in cases of patients diagnosed with familial hypercholesterolemia].
A Kalina, E Czeizel, L Romics, G Pados, I Reiber, A Dósa, I Hermányi, Z Lakatos, J Tarján, E Kollega-Tarsoly,[...]. Orv Hetil 1998
11
90

Report from the workshop on Pallister-Hall syndrome and related phenotypes.
L G Biesecker, M Abbott, J Allen, C Clericuzio, P Feuillan, J M Graham, J Hall, S Kang, A H Olney, D Lefton,[...]. Am J Med Genet 1996
57
40

Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one.
S Fanconi, J A Fischer, P Wieland, M Atares, A Fanconi, A Giedion, A Prader. J Pediatr 1986
40
40

Three novel connexin26 gene mutations in autosomal recessive non-syndromic deafness.
Y Fuse, K Doi, T Hasegawa, A Sugii, H Hibino, T Kubo. Neuroreport 1999
96
40


Turkish Heart Study: lipids, lipoproteins, and apolipoproteins.
R W Mahley, K E Palaoğlu, Z Atak, J Dawson-Pepin, A M Langlois, V Cheung, H Onat, P Fulks, L L Mahley, F Vakar. J Lipid Res 1995
213
40

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
696
40

Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.
D Ford, D F Easton, M Stratton, S Narod, D Goldgar, P Devilee, D T Bishop, B Weber, G Lenoir, J Chang-Claude,[...]. Am J Hum Genet 1998
40

Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia.
R M Scarel, P C Trevilatto, O Di Hipólito, L E Camargo, S R Line. Am J Med Genet 2000
44
40


Neocentromere formation in a stable ring 1p32-p36.1 chromosome.
H R Slater, S Nouri, E Earle, A W Lo, L G Hale, K H Choo. J Med Genet 1999
26
40

Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.
D F Callen, H Eyre, M Y Yip, J Freemantle, E A Haan. Am J Med Genet 1992
127
40

Oligodontia, taurodontia, and sparse hair growth--a syndrome.
K T Moller, R J Gorlin, B Wedge. J Speech Hear Disord 1973
21
47

Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease.
A Tybjaerg-Hansen, R Steffensen, H Meinertz, P Schnohr, B G Nordestgaard. N Engl J Med 1998
159
40

Roberts syndrome: clinical and cytogenetic aspects.
N P Mann, J Fitzsimmons, E Fitzsimmons, P Cooke. J Med Genet 1982
33
40

Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations.
W Liu, D I Smith, K J Rechtzigel, S N Thibodeau, C D James. Nucleic Acids Res 1998
215
40


Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.
T W Depinet, J L Zackowski, W C Earnshaw, S Kaffe, G S Sekhon, R Stallard, B A Sullivan, G H Vance, D L Van Dyke, H F Willard,[...]. Hum Mol Genet 1997
154
40


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.