A citation-based method for searching scientific literature

Cornelia M Ulrich, Alan R Kristal, Emily White, Julie R Hunt, Sharon J Durfy, John D Potter. Community Genet 1998
Times Cited: 50







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



Times Cited
  Times     Co-cited
Similarity


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
145
44


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
263
38

Attitudes about genetic testing for breast-ovarian cancer susceptibility.
C Lerman, M Daly, A Masny, A Balshem. J Clin Oncol 1994
434
34

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
32


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
127
30

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
184
30

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
100
28

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
92
28

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
604
22

Awareness and attitudes concerning BRCA gene testing.
A Mogilner, M Otten, J D Cunningham, S T Brower. Ann Surg Oncol 1998
48
22

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
46
23



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
20

Nager acrofacial dysostosis.
M T McDonald, J L Gorski. J Med Genet 1993
50
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
833
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
173
20



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
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
385
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
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
20

Associated malformations and chromosomal defects in congenital diaphragmatic hernia.
R Bollmann, K Kalache, H Mau, R Chaoui, C Tennstedt. Fetal Diagn Ther 1995
81
20

Associated anomalies in individuals with polydactyly.
E E Castilla, R Lugarinho, M da Graça Dutra, L J Salgado. Am J Med Genet 1998
47
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
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
74
20


[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
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
40
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
96
20


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
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
696
20

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
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
44
22


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
38

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
20

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
20

Roberts syndrome: clinical and cytogenetic aspects.
N P Mann, J Fitzsimmons, E Fitzsimmons, P Cooke. J Med Genet 1982
33
30

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
20



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.