G Evers-Kiebooms, J J Cassiman, H van den Berghe. J Med Genet 1987
Times Cited: 42
Times Cited: 42
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
S Kessler, T Field, L Worth, H Mosbarger. Am J Med Genet 1987
54
Attitudes toward presymptomatic testing in Huntington disease.
C Mastromauro, R H Myers, B Berkman. Am J Med Genet 1987
C Mastromauro, R H Myers, B Berkman. Am J Med Genet 1987
47
Intended use of predictive testing by those at risk for Huntington disease.
G J Meissen, R L Berchek. Am J Med Genet 1987
G J Meissen, R L Berchek. Am J Med Genet 1987
42
Predictive testing for Huntington disease: II. Demographic characteristics, life-style patterns, attitudes, and psychosocial assessments of the first fifty-one test candidates.
M Bloch, M Fahy, S Fox, M R Hayden. Am J Med Genet 1989
M Bloch, M Fahy, S Fox, M R Hayden. Am J Med Genet 1989
42
At-risk persons' attitudes toward presymptomatic and prenatal testing of Huntington disease in Michigan.
D S Markel, A B Young, J B Penney. Am J Med Genet 1987
D S Markel, A B Young, J B Penney. Am J Med Genet 1987
40
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
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
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
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
C Lerman, J Seay, A Balshem, J Audrain. Am J Med Genet 1995
30
BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes.
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C Lerman, S Narod, K Schulman, C Hughes, A Gomez-Caminero, G Bonney, K Gold, B Trock, D Main, J Lynch,[...]. JAMA 1996
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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
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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
28
Uptake of presymptomatic predictive testing for Huntington's disease.
D Craufurd, A Dodge, L Kerzin-Storrar, R Harris. Lancet 1989
D Craufurd, A Dodge, L Kerzin-Storrar, R Harris. Lancet 1989
28
Interest in genetic testing for colon cancer susceptibility: cognitive and emotional correlates.
R T Croyle, C Lerman. Prev Med 1993
R T Croyle, C Lerman. Prev Med 1993
26
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
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
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
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
P B Jacobsen, H B Valdimarsdottier, K L Brown, K Offit. Psychosom Med 1997
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
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
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
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
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
26
A new case of "complete" trisomy 5p with isochromosome 5p associated with a de novo translocation t(5;8)(q11;p23).
M Fujita, E Flori, F Lemaire, R Casanova, D Astruc. Clin Genet 1994
M Fujita, E Flori, F Lemaire, R Casanova, D Astruc. Clin Genet 1994
47
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
Y Goto, I Nonaka, S Horai. Nature 1990
Y Goto, I Nonaka, S Horai. Nature 1990
23
Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region.
W P Robinson, M Lalande. Hum Mol Genet 1995
W P Robinson, M Lalande. Hum Mol Genet 1995
23
On two patients with and without the classical Wolf-Hirschhorn syndrome (WHS) sharing the same chromosome 4p16.3 specific probe deletion: evidence of a contiguous gene deletion syndrome.
P Petit, J Schmit, H Van den Berghe, J P Fryns. Clin Genet 1996
P Petit, J Schmit, H Van den Berghe, J P Fryns. Clin Genet 1996
40
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
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
23
Macrocephaly and dilated Virchow-Robin spaces in childhood.
J Artigas, P Poo, A Rovira, E Cardo. Pediatr Radiol 1999
J Artigas, P Poo, A Rovira, E Cardo. Pediatr Radiol 1999
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
C Stolle, G Glenn, B Zbar, J S Humphrey, P Choyke, M Walther, S Pack, K Hurley, C Andrey, R Klausner,[...]. Hum Mutat 1998
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Trisomy 20p due to a paternal reciprocal translocation.
S J Funderburk, R S Sparkes, M C Sparkes. Ann Genet 1983
S J Funderburk, R S Sparkes, M C Sparkes. Ann Genet 1983
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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
J M Hall, M K Lee, B Newman, J E Morrow, L A Anderson, B Huey, M C King. Science 1990
23
Whole mitochondrial genome amplification reveals basal level multiple deletions in mtDNA of patients with dilated cardiomyopathy.
Y Y Li, C Hengstenberg, B Maisch. Biochem Biophys Res Commun 1995
Y Y Li, C Hengstenberg, B Maisch. Biochem Biophys Res Commun 1995
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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
A Torroni, K Huoponen, P Francalacci, M Petrozzi, L Morelli, R Scozzari, D Obinu, M L Savontaus, D C Wallace. Genetics 1996
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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
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
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
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
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
M Dasouki, V Jurecic, J A Phillips, J A Whitlock, A Baldini. Am J Med Genet 1997
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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
E Rossi, G Floridia, M Casali, C Danesino, G Chiumello, F Bernardi, I Magnani, L Papi, M Mura, O Zuffardi. J Med Genet 1993
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Third International Meeting on von Hippel-Lindau disease.
B Zbar, W Kaelin, E Maher, S Richard. Cancer Res 1999
B Zbar, W Kaelin, E Maher, S Richard. Cancer Res 1999
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Retinal angiomatosis: the ocular manifestations of von Hippel-Lindau disease.
M Ridley, J Green, G Johnson. Can J Ophthalmol 1986
M Ridley, J Green, G Johnson. Can J Ophthalmol 1986
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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
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
30
The psychosocial impact of mass screening for cardiovascular risk factors.
T Tymstra, B Bieleman. Fam Pract 1987
T Tymstra, B Bieleman. Fam Pract 1987
23
Duplication 20p identified via fluorescent in situ hybridization.
K A LeChien, E McPherson, A M Estop. Am J Med Genet 1994
K A LeChien, E McPherson, A M Estop. Am J Med Genet 1994
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
M Levy, Y Pirson, P Simon, B Boudailliez, H Nivet, N Rancé, A Moynot, M Broyer, J P Grünfeld. Clin Nephrol 1994
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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
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
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Immunological and neuropathological significance of the Virchow-Robin space.
M M Esiri, D Gay. J Neurol Sci 1990
M M Esiri, D Gay. J Neurol Sci 1990
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Wolfram's syndrome: a clinical, diagnostic, and interpretative contribution.
C Blasi, F Pierelli, E Rispoli, M Saponara, E Vingolo, D Andreani. Diabetes Care 1986
C Blasi, F Pierelli, E Rispoli, M Saponara, E Vingolo, D Andreani. Diabetes Care 1986
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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
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
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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
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
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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
J Kohlhase, A Wischermann, H Reichenbach, U Froster, W Engel. Nat Genet 1998
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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
S C Daw, C Taylor, M Kraman, K Call, J Mao, S Schuffenhauer, T Meitinger, T Lipson, J Goodship, P Scambler. Nat Genet 1996
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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
I W Lurie, M F Schwartz, S Schwartz, M M Cohen. Am J Med Genet 1995
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
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
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.