A citation-based method for searching scientific literature

G Evers-Kiebooms, J J Cassiman, H van den Berghe. J Med Genet 1987
Times Cited: 42







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



Times Cited
  Times     Co-cited
Similarity


Attitudes of persons at risk for Huntington disease toward predictive testing.
S Kessler, T Field, L Worth, H Mosbarger. Am J Med Genet 1987
159
54

Attitudes toward presymptomatic testing in Huntington disease.
C Mastromauro, R H Myers, B Berkman. Am J Med Genet 1987
127
47




A polymorphic DNA marker genetically linked to Huntington's disease.
J F Gusella, N S Wexler, P M Conneally, S L Naylor, M A Anderson, R E Tanzi, P C Watkins, K Ottina, M R Wallace, A Y Sakaguchi. Nature 1983
40

Predictive testing for Huntington's disease: risk perception, reasons for testing and psychological profile of test applicants.
M Decruyenaere, G Evers-Kiebooms, A Boogaerts, J J Cassiman, T Cloostermans, K Demyttenaere, R Dom, J P Fryns, H Van den Berghe. Genet Couns 1995
69
35

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
30

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
28

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
28

Attitudes about genetic testing for breast-ovarian cancer susceptibility.
C Lerman, M Daly, A Masny, A Balshem. J Clin Oncol 1994
434
28

Uptake of presymptomatic predictive testing for Huntington's disease.
D Craufurd, A Dodge, L Kerzin-Storrar, R Harris. Lancet 1989
181
28


Identification of the breast cancer susceptibility gene BRCA2.
R Wooster, G Bignell, J Lancaster, S Swift, S Seal, J Mangion, N Collins, S Gregory, C Gumbs, G Micklem. Nature 1995
26

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
26

Impact of Event Scale: a measure of subjective stress.
M Horowitz, N Wilner, W Alvarez. Psychosom Med 1979
26

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
26

A descriptive study of BRCA1 testing and reactions to disclosure of test results.
H T Lynch, S J Lemon, C Durham, S T Tinley, C Connolly, J F Lynch, J Surdam, E Orinion, S Slominski-Caster, P Watson,[...]. Cancer 1997
169
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
128
26

Predictive testing for Huntington's disease with use of a linked DNA marker.
G J Meissen, R H Myers, C A Mastromauro, W J Koroshetz, K W Klinger, L A Farrer, P A Watkins, J F Gusella, E D Bird, J B Martin. N Engl J Med 1988
156
26





Townes-Brocks syndrome: detection of a SALL1 mutation hot spot and evidence for a position effect in one patient.
S Marlin, S Blanchard, R Slim, D Lacombe, F Denoyelle, J L Alessandri, E Calzolari, V Drouin-Garraud, F G Ferraz, A Fourmaintraux,[...]. Hum Mutat 1999
55
23

Macrocephaly and dilated Virchow-Robin spaces in childhood.
J Artigas, P Poo, A Rovira, E Cardo. Pediatr Radiol 1999
29
34

Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene.
C Stolle, G Glenn, B Zbar, J S Humphrey, P Choyke, M Walther, S Pack, K Hurley, C Andrey, R Klausner,[...]. Hum Mutat 1998
331
23

Trisomy 20p due to a paternal reciprocal translocation.
S J Funderburk, R S Sparkes, M C Sparkes. Ann Genet 1983
25
40

Linkage of early-onset familial breast cancer to chromosome 17q21.
J M Hall, M K Lee, B Newman, J E Morrow, L A Anderson, B Huey, M C King. Science 1990
23


Classification of European mtDNAs from an analysis of three European populations.
A Torroni, K Huoponen, P Francalacci, M Petrozzi, L Morelli, R Scozzari, D Obinu, M L Savontaus, D C Wallace. Genetics 1996
601
23

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
B Zbar, T Kishida, F Chen, L Schmidt, E R Maher, F M Richards, P A Crossey, A R Webster, N A Affara, M A Ferguson-Smith,[...]. Hum Mutat 1996
386
23

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region.
T J Wright, D O Ricke, K Denison, S Abmayr, P D Cotter, K Hirschhorn, M Keinänen, D McDonald-McGinn, M Somer, N Spinner,[...]. Hum Mol Genet 1997
179
23

DiGeorge anomaly and chromosome 10p deletions: one or two loci?
M Dasouki, V Jurecic, J A Phillips, J A Whitlock, A Baldini. Am J Med Genet 1997
28
35

Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.
E Rossi, G Floridia, M Casali, C Danesino, G Chiumello, F Bernardi, I Magnani, L Papi, M Mura, O Zuffardi. J Med Genet 1993
78
23

Third International Meeting on von Hippel-Lindau disease.
B Zbar, W Kaelin, E Maher, S Richard. Cancer Res 1999
48
23


Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p 16.3.
S G Kant, A Van Haeringen, E Bakker, I Stec, D Donnai, P Mollevanger, G C Beverstock, M C Lindeman-Kusse, G J Van Ommen. J Med Genet 1997
33
30


Duplication 20p identified via fluorescent in situ hybridization.
K A LeChien, E McPherson, A M Estop. Am J Med Genet 1994
19
52

Evaluation in patients with Alport syndrome of knowledge of the disease and attitudes toward prenatal diagnosis.
M Levy, Y Pirson, P Simon, B Boudailliez, H Nivet, N Rancé, A Moynot, M Broyer, J P Grünfeld. Clin Nephrol 1994
28
35

Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.
S Demczuk, A Lévy, M Aubry, M F Croquette, N Philip, M Prieur, U Sauer, P Bouvagnet, G A Rouleau, G Thomas. Hum Genet 1995
50
23


Wolfram's syndrome: a clinical, diagnostic, and interpretative contribution.
C Blasi, F Pierelli, E Rispoli, M Saponara, E Vingolo, D Andreani. Diabetes Care 1986
53
23

A common molecular basis for rearrangement disorders on chromosome 22q11.
L Edelmann, R K Pandita, E Spiteri, B Funke, R Goldberg, N Palanisamy, R S Chaganti, E Magenis, R J Shprintzen, B E Morrow. Hum Mol Genet 1999
340
23

A genetic register for von Hippel-Lindau disease.
I R Maddock, A Moran, E R Maher, M D Teare, A Norman, S J Payne, R Whitehouse, C Dodd, M Lavin, N Hartley,[...]. J Med Genet 1996
172
23

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.
J Kohlhase, A Wischermann, H Reichenbach, U Froster, W Engel. Nat Genet 1998
335
23

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes.
S C Daw, C Taylor, M Kraman, K Call, J Mao, S Schuffenhauer, T Meitinger, T Lipson, J Goodship, P Scambler. Nat Genet 1996
149
23

Trisomy 7p resulting from isochromosome formation and whole-arm translocation.
I W Lurie, M F Schwartz, S Schwartz, M M Cohen. Am J Med Genet 1995
40
25

Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders.
C Carlson, D Papolos, R K Pandita, G L Faedda, S Veit, R Goldberg, R Shprintzen, R Kucherlapati, B Morrow. Am J Hum Genet 1997
122
23


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.