A citation-based method for searching scientific literature

Milena Paneque, Carolina Lemos, Karell Escalona, Lizandra Prieto, Rubén Reynaldo, Mercedes Velázquez, Judith Quevedo, Nieves Santos, Luis Enrique Almaguer, Luis Velázquez, Alda Sousa, Manuela Fleming, Jorge Sequeiros. J Genet Couns 2007
Times Cited: 11







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



Times Cited
  Times     Co-cited
Similarity


Psychological aspects of presymptomatic diagnosis of spinocerebellar ataxia type 2 in Cuba.
H M Paneque, A L Prieto, R R Reynaldo, M T Cruz, F N Santos, M L Almaguer, P L Velázquez, B L Heredero. Community Genet 2007
18
72



Long-term outcome of presymptomatic testing in Huntington disease.
Marcela Gargiulo, Séverine Lejeune, Marie-Laure Tanguy, Khadija Lahlou-Laforêt, Anne Faudet, David Cohen, Josué Feingold, Alexandra Durr. Eur J Hum Genet 2009
63
45

Presymptomatic testing for neurogenetic diseases in Brazil: assessing who seeks and who follows through with testing.
Caroline Santa Maria Rodrigues, Viviane Ziebell de Oliveira, Gabriela Camargo, Claudio Maria da Silva Osório, Raphael Machado de Castilhos, Maria Luiza Saraiva-Pereira, Lavínia Schuler-Faccini, Laura Bannach Jardim. J Genet Couns 2012
24
45

Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.
S M Pulst, A Nechiporuk, T Nechiporuk, S Gispert, X N Chen, I Lopes-Cendes, S Pearlman, S Starkman, G Orozco-Diaz, A Lunkes,[...]. Nat Genet 1996
893
36


Predictive testing for Huntington's disease.
Aad Tibben. Brain Res Bull 2007
83
36

Molecular epidemiology of spinocerebellar ataxias in Cuba: insights into SCA2 founder effect in Holguin.
Luis Velázquez Pérez, Gilberto Sánchez Cruz, Nieves Santos Falcón, Luis Enrique Almaguer Mederos, Karel Escalona Batallan, Roberto Rodríguez Labrada, Milena Paneque Herrera, José Miguel Laffita Mesa, Julio C Rodríguez Díaz, Raúl Aguilera Rodríguez,[...]. Neurosci Lett 2009
75
36

Presymptomatic diagnosis in Huntington's disease: the Mexican experience.
Maria Elisa Alonso, Adriana Ochoa, Ana Luisa Sosa, Yaneth Rodríguez, Mireya Chávez, Catherine Boll, Petra Yescas, Rosario Macías, Astrid Rasmussen. Genet Test Mol Biomarkers 2009
16
36

Presymptomatic tests in Huntington's disease and dominant ataxias.
M Cannella, M Simonelli, C D'Alessio, F Pierelli, S Ruggieri, F Squitieri. Neurol Sci 2001
16
36

Disease knowledge and attitudes toward predictive testing and prenatal diagnosis in families with Machado-Joseph disease from the Azores Islands (Portugal).
M Lima, T Kay, J Vasconcelos, L Mota-Vieira, C Gonzalez, A Peixoto, A Abade, P MacLeod, R Graca, J Santos. Community Genet 2001
11
36

Experience over fifteen years with a protocol for predictive testing for Huntington disease.
Suzanne Dufrasne, Madeleine Roy, Maria Galvez, David S Rosenblatt. Mol Genet Metab 2011
54
36

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.
K Sanpei, H Takano, S Igarashi, T Sato, M Oyake, H Sasaki, A Wakisaka, K Tashiro, Y Ishida, T Ikeuchi,[...]. Nat Genet 1996
624
27

Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
27

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
G Imbert, F Saudou, G Yvert, D Devys, Y Trottier, J M Garnier, C Weber, J L Mandel, G Cancel, N Abbas,[...]. Nat Genet 1996
719
27

Short-term psychological impact of predictive testing for Machado-Joseph disease: depression and anxiety levels in individuals at risk from the Azores (Portugal).
Carlos Gonzalez, Manuela Lima, Teresa Kay, Catarina Silva, Cristina Santos, Jorge Santos. Community Genet 2004
11
27

The psychological consequences of predictive testing for Huntington's disease. Canadian Collaborative Study of Predictive Testing.
S Wiggins, P Whyte, M Huggins, S Adam, J Theilmann, M Bloch, S B Sheps, M T Schechter, M R Hayden. N Engl J Med 1992
348
27


Ethical dilemmas in genetic testing: examples from the Cuban program for predictive diagnosis of hereditary ataxias.
Tania Cruz Mariño, Rubén Reynaldo Armiñán, Humberto Jorge Cedeño, José Miguel Laffita Mesa, Yanetza González Zaldivar, Raúl Aguilera Rodríguez, Miguel Velázquez Santos, Luis Enrique Almaguer Mederos, Milena Paneque Herrera, Luis Velázquez Pérez. J Genet Couns 2011
9
33

Recommendations for the predictive genetic test in Huntington's disease.
R MacLeod, A Tibben, M Frontali, G Evers-Kiebooms, A Jones, A Martinez-Descales, R A Roos. Clin Genet 2013
120
27

Predictive testing for Huntington disease in a developing country.
M J Futter, J M Heckmann, L J Greenberg. Clin Genet 2009
14
27

Decreasing uptake of predictive testing for Huntington's disease in a German centre: 12 years' experience (1993-2004).
Christiane Bernhardt, Anne-Marie Schwan, Peter Kraus, Joerg Thomas Epplen, Erdmute Kunstmann. Eur J Hum Genet 2009
27
27

The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from.
T Cruz-Mariño, L Velázquez-Pérez, Y González-Zaldivar, R Aguilera-Rodríguez, M Velázquez-Santos, Y Vázquez-Mojena, A Estupiñán-Rodríguez, J M Laffita-Mesa, R Reynaldo-Armiñán, L E Almaguer-Mederos,[...]. Clin Genet 2013
13
27

Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
G Cancel, A Dürr, O Didierjean, G Imbert, K Bürk, A Lezin, S Belal, A Benomar, M Abada-Bendib, C Vial,[...]. Hum Mol Genet 1997
193
18

Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2.
Luis Velázquez Pérez, Gilberto Sánchez Cruz, Nalia Canales Ochoa, Roberto Rodríguez Labrada, Julio Rodríguez Díaz, Luis Almaguer Mederos, José Laffita Mesa. J Neurol Sci 2007
37
18

Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes.
Terrence F Satterfield, Leo J Pallanck. Hum Mol Genet 2006
131
18

The parkinsonian phenotype of spinocerebellar ataxia type 2.
Chin-Song Lu, Yah-Huei Wu Chou, Pei-Chi Kuo, Hsiu-Chen Chang, Yi-Hsin Weng. Arch Neurol 2004
70
18

Saccade velocity as a surrogate disease marker in spinocerebellar ataxia type 2.
C Seifried, L Velázquez-Pérez, N Santos-Falcón, M Abele, U Ziemann, L E Almaguer, E Martínez-Góngora, G Sánchez-Cruz, N Canales, R Pérez-González,[...]. Ann N Y Acad Sci 2005
17
18

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.
G Orozco, R Estrada, T L Perry, J Araña, R Fernandez, A Gonzalez-Quevedo, J Galarraga, S Hansen. J Neurol Sci 1989
148
18

Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules.
Ute Nonhoff, Markus Ralser, Franziska Welzel, Ilaria Piccini, Daniela Balzereit, Marie-Laure Yaspo, Hans Lehrach, Sylvia Krobitsch. Mol Biol Cell 2007
231
18

Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsies.
R Estrada, J Galarraga, G Orozco, A Nodarse, G Auburger. Acta Neuropathol 1999
163
18

Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
Stefan-M Pulst, Nieves Santos, Dai Wang, Huiying Yang, Duong Huynh, Luis Velazquez, K Pattie Figueroa. Brain 2005
95
18

Saccade velocity is controlled by polyglutamine size in spinocerebellar ataxia 2.
Luis Velázquez-Pérez, Carola Seifried, Nieves Santos-Falcón, Michael Abele, Ulf Ziemann, Luis Enrique Almaguer, Edilberto Martínez-Góngora, Gilberto Sánchez-Cruz, Nalia Canales, Ruth Pérez-González,[...]. Ann Neurol 2004
68
18

Uncommon features in Cuban families affected with Friedreich ataxia.
Tania Cruz-Mariño, Yanetza González-Zaldivar, Jose Miguel Laffita-Mesa, Luis Almaguer-Mederos, Raul Aguilera-Rodríguez, Dennis Almaguer-Gotay, Roberto Rodríguez-Labrada, Nalia Canales-Ochoa, Patrick Macleod, Luis Velázquez-Pérez. Neurosci Lett 2010
8
25


[Type 2 spinocerebellar ataxia: acceptance of prenatal diagnosis in descendents at risk].
H M Paneque, F N Santos, C H Tamayo, A R Reynaldo, L Velázquez Pérez, L Almaguer Mederos, R Hechavarría, F T Mouriño, M T Cruz. Rev Neurol 2001
5
40

Working towards ethical management of genetic testing.
Michael Parker, Anneke Lucassen. Lancet 2002
16
18

Progression markers of Spinocerebellar ataxia 2. A twenty years neurophysiological follow up study.
Luis Velázquez-Perez, Roberto Rodríguez-Labrada, Nalia Canales-Ochoa, Gilberto Sanchez-Cruz, Juan Fernandez-Ruiz, Jacqueline Medrano Montero, Raúl Aguilera-Rodríguez, Rosalinda Diaz, Luis E Almaguer-Mederos, Agustín Palomino Truitz. J Neurol Sci 2010
34
18

[Mental disorders in patients with spinocerebellar ataxia type 2 in Cuba].
R D Reynaldo-Armiñán, R Reynaldo-Hernández, M Paneque-Herrera, L Prieto-Avila, E Pérez-Ruiz. Rev Neurol 2002
10
20

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1.
S Gispert, R Twells, G Orozco, A Brice, J Weber, L Heredero, K Scheufler, B Riley, R Allotey, C Nothers. Nat Genet 1993
293
18

Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
Elisa Alonso, Leticia Martínez-Ruano, Irene De Biase, Christopher Mader, Adriana Ochoa, Petra Yescas, Roxana Gutiérrez, Misti White, Luís Ruano, Marcela Fragoso-Benítez,[...]. Mov Disord 2007
33
18

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3.
K Bürk, C Globas, S Bösch, T Klockgether, C Zühlke, I Daum, J Dichgans. J Neurol 2003
138
18

Cognitive findings in spinocerebellar ataxia type 2: relationship to genetic and clinical variables.
Francesco Le Pira, Giuseppe Zappalà, Riccardo Saponara, Elisabetta Domina, Domenico Restivo, Ester Reggio, Alessandra Nicoletti, Salvatore Giuffrida. J Neurol Sci 2002
49
18

Pontine and cerebellar atrophy correlate with clinical disability in SCA2.
S H Ying, S I Choi, S L Perlman, R W Baloh, D S Zee, A W Toga. Neurology 2006
28
18



Five year study of prenatal testing for Huntington's disease: demand, attitudes, and psychological assessment.
S Adam, S Wiggins, P Whyte, M Bloch, M H Shokeir, H Soltan, W Meschino, A Summers, O Suchowersky, J P Welch. J Med Genet 1993
75
18

Depressive symptoms in Machado-Joseph disease (SCA3) patients and their relatives.
C R Cecchin, A P Pires, C R Rieder, T L Monte, I Silveira, T Carvalho, M L Saraiva-Pereira, J Sequeiros, L B Jardim. Community Genet 2007
37
18

Psychological consequences of predictive genetic testing: a systematic review.
M Broadstock, S Michie, T Marteau. Eur J Hum Genet 2000
242
18


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.