A Mogilner, M Otten, J D Cunningham, S T Brower. Ann Surg Oncol 1998
Times Cited: 48
Times Cited: 48
Times Cited
Times Co-cited
Similarity
Genetic testing for breast cancer susceptibility: awareness and interest among women in the general population.
E S Tambor, B K Rimer, T S Strigo. Am J Med Genet 1997
E S Tambor, B K Rimer, T S Strigo. Am J Med Genet 1997
62
Interest in genetic testing among first-degree relatives of breast cancer patients.
C Lerman, J Seay, A Balshem, J Audrain. Am J Med Genet 1995
C Lerman, J Seay, A Balshem, J Audrain. Am J Med Genet 1995
52
Attitudes and interest in genetic testing for breast and ovarian cancer susceptibility in diverse groups of women in western Washington.
S J Durfy, D J Bowen, A McTiernan, J Sporleder, W Burke. Cancer Epidemiol Biomarkers Prev 1999
S J Durfy, D J Bowen, A McTiernan, J Sporleder, W Burke. Cancer Epidemiol Biomarkers Prev 1999
47
Interest in learning of personal genetic risk for cancer: a general population survey.
M A Andrykowski, R K Munn, J L Studts. Prev Med 1996
M A Andrykowski, R K Munn, J L Studts. Prev Med 1996
47
Attitudes about genetic testing for breast-ovarian cancer susceptibility.
C Lerman, M Daly, A Masny, A Balshem. J Clin Oncol 1994
C Lerman, M Daly, A Masny, A Balshem. J Clin Oncol 1994
47
Anticipated uptake and impact of genetic testing in hereditary breast and ovarian cancer families.
J P Struewing, C Lerman, R G Kase, T R Giambarresi, M A Tucker. Cancer Epidemiol Biomarkers Prev 1995
J P Struewing, C Lerman, R G Kase, T R Giambarresi, M A Tucker. Cancer Epidemiol Biomarkers Prev 1995
45
Decision-making about genetic testing among women at familial risk for breast cancer.
P B Jacobsen, H B Valdimarsdottier, K L Brown, K Offit. Psychosom Med 1997
P B Jacobsen, H B Valdimarsdottier, K L Brown, K Offit. Psychosom Med 1997
39
Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.
M Cappelli, L Surh, L Humphreys, S Verma, D Logan, A Hunter, J Allanson. Clin Genet 1999
M Cappelli, L Surh, L Humphreys, S Verma, D Logan, A Hunter, J Allanson. Clin Genet 1999
37
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
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Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium.
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29
Attitudes towards cancer predictive testing and transmission of information to the family.
C Julian-Reynier, F Eisinger, P Vennin, F Chabal, Y Aurran, C Noguès, Y J Bignon, M Machelard-Roumagnac, C Maugard-Louboutin, D Serin,[...]. J Med Genet 1996
C Julian-Reynier, F Eisinger, P Vennin, F Chabal, Y Aurran, C Noguès, Y J Bignon, M Machelard-Roumagnac, C Maugard-Louboutin, D Serin,[...]. J Med Genet 1996
29
BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.
C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, G Bonney, K Gold, B Trock, D Main, J Lynch,[...]. JAMA 1996
C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, G Bonney, K Gold, B Trock, D Main, J Lynch,[...]. JAMA 1996
27
Ethnic differences in knowledge and attitudes about BRCA1 testing in women at increased risk.
C Hughes, A Gomez-Caminero, J Benkendorf, J Kerner, C Isaacs, J Barter, C Lerman. Patient Educ Couns 1997
C Hughes, A Gomez-Caminero, J Benkendorf, J Kerner, C Isaacs, J Barter, C Lerman. Patient Educ Couns 1997
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Attitudes to genetic testing for breast cancer susceptibility in women at increased risk developing hereditary breast cancer.
B Meiser, P Butow, A Barratt, G Suthers, M Smith, A Colley, E Thompson, K Tucker. J Med Genet 2000
B Meiser, P Butow, A Barratt, G Suthers, M Smith, A Colley, E Thompson, K Tucker. J Med Genet 2000
26
Women's receptivity to testing for a genetic susceptibility to breast cancer.
H Chaliki, S Loader, J C Levenkron, W Logan-Young, W J Hall, P T Rowley. Am J Public Health 1995
H Chaliki, S Loader, J C Levenkron, W Logan-Young, W J Hall, P T Rowley. Am J Public Health 1995
22
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
22
Genetic testing for cancer risk: a population survey on attitudes and intention.
Cornelia M Ulrich, Alan R Kristal, Emily White, Julie R Hunt, Sharon J Durfy, John D Potter. Community Genet 1998
Cornelia M Ulrich, Alan R Kristal, Emily White, Julie R Hunt, Sharon J Durfy, John D Potter. Community Genet 1998
22
Comparison of the pattern of agenesis in the primary and permanent dentitions in a population characterized by agenesis in the primary dentition.
J Daugaard-Jensen, M Nodal, L T Skovgaard, I Kjaer. Int J Paediatr Dent 1997
J Daugaard-Jensen, M Nodal, L T Skovgaard, I Kjaer. Int J Paediatr Dent 1997
40
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
30
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
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20
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
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20
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
20
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
20
Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.
E Hatchwell. J Med Genet 1996
E Hatchwell. J Med Genet 1996
27
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
20
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
20
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
20
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
20
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
21
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
20
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
22
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
20
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
20
Acquisition and metastability of centromere identity and function: sequence analysis of a human neocentromere.
K A Maggert, G H Karpen. Genome Res 2000
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[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
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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
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20
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
25
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
20
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
31
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
20
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
20
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
22
BRCA1 and BRCA2 testing: weighing the demand against the benefits.
P Devilee. Am J Hum Genet 1999
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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
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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
20
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
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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
30
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.