J Daugaard-Jensen, M Nodal, L T Skovgaard, I Kjaer. Int J Paediatr Dent 1997
Times Cited: 25
Times Cited: 25
Times Cited
Times Co-cited
Similarity
Aplasia, supernumerary teeth and fused teeth in the primary dentition. An epidemiologic study.
J J Ravn. Scand J Dent Res 1971
J J Ravn. Scand J Dent Res 1971
64
Supernumerary and congenitally missing primary teeth in Finnish children. An epidemiologic study.
S Järvinen, L Lehtinen. Acta Odontol Scand 1981
S Järvinen, L Lehtinen. Acta Odontol Scand 1981
60
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
H Vastardis, N Karimbux, S W Guthua, J G Seidman, C E Seidman. Nat Genet 1996
56
On the genetics of hypodontia and microdontia: synergism or allelism of major genes in a family with six affected members.
S P Lyngstadaas, H Nordbo, T Gedde-Dahl, P S Thrane. J Med Genet 1996
S P Lyngstadaas, H Nordbo, T Gedde-Dahl, P S Thrane. J Med Genet 1996
52
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
P Nieminen, S Arte, S Pirinen, L Peltonen, I Thesleff. Hum Genet 1995
52
Palatal displacement of canine is genetic and related to congenital absence of teeth.
S Pirinen, S Arte, S Apajalahti. J Dent Res 1996
S Pirinen, S Arte, S Apajalahti. J Dent Res 1996
52
Dominant inheritance of tooth malpositions and their association to hypodontia.
E Svinhufvud, S Myllärniemi, R Norio. Clin Genet 1988
E Svinhufvud, S Myllärniemi, R Norio. Clin Genet 1988
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
S Arte, P Nieminen, S Pirinen, I Thesleff, L Peltonen. J Dent Res 1996
48
Hypodontia, hyperodontia, and double formation of primary teeth in Iceland. An epidemiological study.
T E Magnússon. Acta Odontol Scand 1984
T E Magnússon. Acta Odontol Scand 1984
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
M J van den Boogaard, M Dorland, F A Beemer, H K van Amstel. Nat Genet 2000
44
Short root anomaly in families and its association with other dental anomalies.
S Apajalahti, S Arte, S Pirinen. Eur J Oral Sci 1999
S Apajalahti, S Arte, S Pirinen. Eur J Oral Sci 1999
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
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
44
The inheritance pattern of missing, peg-shaped, and strongly mesio-distally reduced upper lateral incisors.
L Alvesalo, P Portin. Acta Odontol Scand 1969
L Alvesalo, P Portin. Acta Odontol Scand 1969
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
R Döffinger, A Smahi, C Bessia, F Geissmann, J Feinberg, A Durandy, C Bodemer, S Kenwrick, S Dupuis-Girod, S Blanche,[...]. Nat Genet 2001
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
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
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
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
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
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
40
Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis.
A C Jones, J Austin, N Hansen, B Hoogendoorn, P J Oefner, J P Cheadle, M C O'Donovan. Clin Chem 1999
A C Jones, J Austin, N Hansen, B Hoogendoorn, P J Oefner, J P Cheadle, M C O'Donovan. Clin Chem 1999
40
Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.
E Hatchwell. J Med Genet 1996
E Hatchwell. J Med Genet 1996
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
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
40
A de novo 13 nt deletion, a newly identified C647W missense mutation and a deletion of exon 18 in infantile onset glycogen storage disease type II (GSDII).
M L Huie, A S Chen, S S Brooks, A Grix, R Hirschhorn. Hum Mol Genet 1994
M L Huie, A S Chen, S S Brooks, A Grix, R Hirschhorn. Hum Mol Genet 1994
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
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
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
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
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
A Kuklin, K Munson, D Gjerde, R Haefele, P Taylor. Genet Test 1997
40
Associated malformations and chromosomal defects in congenital diaphragmatic hernia.
R Bollmann, K Kalache, H Mau, R Chaoui, C Tennstedt. Fetal Diagn Ther 1995
R Bollmann, K Kalache, H Mau, R Chaoui, C Tennstedt. Fetal Diagn Ther 1995
40
Associated anomalies in individuals with polydactyly.
E E Castilla, R Lugarinho, M da Graça Dutra, L J Salgado. Am J Med Genet 1998
E E Castilla, R Lugarinho, M da Graça Dutra, L J Salgado. Am J Med Genet 1998
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
S A Miller, D D Dykes, H F Polesky. Nucleic Acids Res 1988
40
Restriction fragment length polymorphisms of apolipoprotein B gene in Chinese population with coronary heart disease.
J P Pan, A N Chiang, J J Tai, S P Wang, M S Chang. Clin Chem 1995
J P Pan, A N Chiang, J J Tai, S P Wang, M S Chang. Clin Chem 1995
40
Acro-renal-ocular syndrome: autosomal dominant thumb hypoplasia, renal ectopia, and eye defect.
F Halal, M Homsy, G Perreault. Am J Med Genet 1984
F Halal, M Homsy, G Perreault. Am J Med Genet 1984
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
D T Howe, M D Kilby, H Sirry, G M Barker, E Roberts, E V Davison, J Mchugo, M J Whittle. Prenat Diagn 1996
40
Acquisition and metastability of centromere identity and function: sequence analysis of a human neocentromere.
K A Maggert, G H Karpen. Genome Res 2000
K A Maggert, G H Karpen. Genome Res 2000
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
A Kalina, E Czeizel, L Romics, G Pados, I Reiber, A Dósa, I Hermányi, Z Lakatos, J Tarján, E Kollega-Tarsoly,[...]. Orv Hetil 1998
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
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
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
S Fanconi, J A Fischer, P Wieland, M Atares, A Fanconi, A Giedion, A Prader. J Pediatr 1986
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
Y Fuse, K Doi, T Hasegawa, A Sugii, H Hibino, T Kubo. Neuroreport 1999
40
Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.
H F Sutherland, U J Kim, P J Scambler. Genomics 1998
H F Sutherland, U J Kim, P J Scambler. Genomics 1998
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
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
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
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
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
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
R M Scarel, P C Trevilatto, O Di Hipólito, L E Camargo, S R Line. Am J Med Genet 2000
40
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
H R Slater, S Nouri, E Earle, A W Lo, L G Hale, K H Choo. J Med Genet 1999
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
D F Callen, H Eyre, M Y Yip, J Freemantle, E A Haan. Am J Med Genet 1992
40
Oligodontia, taurodontia, and sparse hair growth--a syndrome.
K T Moller, R J Gorlin, B Wedge. J Speech Hear Disord 1973
K T Moller, R J Gorlin, B Wedge. J Speech Hear Disord 1973
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
A Tybjaerg-Hansen, R Steffensen, H Meinertz, P Schnohr, B G Nordestgaard. N Engl J Med 1998
40
Roberts syndrome: clinical and cytogenetic aspects.
N P Mann, J Fitzsimmons, E Fitzsimmons, P Cooke. J Med Genet 1982
N P Mann, J Fitzsimmons, E Fitzsimmons, P Cooke. J Med Genet 1982
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
W Liu, D I Smith, K J Rechtzigel, S N Thibodeau, C D James. Nucleic Acids Res 1998
40
Familial defective apolipoprotein B-100: a mutation emerged in the mesolithic ancestors of Celtic peoples?
A R Miserez, P Y Muller. Atherosclerosis 2000
A R Miserez, P Y Muller. Atherosclerosis 2000
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
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
40
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