A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity



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
115
42


Genetic counseling globally: Where are we now?
Kelly E Ormond, Mercy Ygoña Laurino, Kristine Barlow-Stewart, Tina-Marié Wessels, Shelley Macaulay, Jehannine Austin, Anna Middleton. Am J Med Genet C Semin Med Genet 2018
52
42

Genetic counselor perceptions of genetic counseling session goals: a validation study of the reciprocal-engagement model.
Julianne E Hartmann, Patricia McCarthy Veach, Ian M MacFarlane, Bonnie S LeRoy. J Genet Couns 2015
28
42




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
28

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
28

Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy.
Teresa Coelho, Luis F Maia, Ana Martins da Silva, Márcia W Cruz, Violaine Planté-Bordeneuve, Ole B Suhr, Isabel Conceiçao, Hartmut H-J Schmidt, Pedro Trigo, Jeffery W Kelly,[...]. J Neurol 2013
212
28

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
28


Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors.
Jill S Goldman, Susan E Hahn, Jennifer Williamson Catania, Susan LaRusse-Eckert, Melissa Barber Butson, Malia Rumbaugh, Michelle N Strecker, J Scott Roberts, Wylie Burke, Richard Mayeux,[...]. Genet Med 2011
171
28

Genetic Counseling in Portugal: Education, Practice and a Developing Profession.
Milena Paneque, Álvaro Mendes, Jorge Saraiva, Jorge Sequeiros. J Genet Couns 2015
8
28

Operationalizing the Reciprocal Engagement Model of Genetic Counseling Practice: a Framework for the Scalable Delivery of Genomic Counseling and Testing.
Tara Schmidlen, Amy C Sturm, Shelly Hovick, Laura Scheinfeldt, J Scott Roberts, Lindsey Morr, Joseph McElroy, Amanda E Toland, Michael Christman, Julianne M O'Daniel,[...]. J Genet Couns 2018
15
28

Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
140
28

Defining Our Clinical Practice: The Identification of Genetic Counseling Outcomes Utilizing the Reciprocal Engagement Model.
Krista Redlinger-Grosse, Patricia McCarthy Veach, Stephanie Cohen, Bonnie S LeRoy, Ian M MacFarlane, Heather Zierhut. J Genet Couns 2016
24
28

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
375
28

Quality issues concerning genetic counselling for presymptomatic testing: a European Delphi study.
Milena Paneque, Jorge Sequeiros, Heather Skirton. Eur J Hum Genet 2015
8
28

Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.
Maria do Carmo Costa, Paula Magalhães, Fátima Ferreirinha, Laura Guimarães, Cristina Januário, Isabel Gaspar, Leal Loureiro, José Vale, Carolina Garrett, Fernando Regateiro,[...]. Eur J Hum Genet 2003
17
14

A profile of the genetic counsellor and genetic nurse profession in European countries.
Cristophe Cordier, Debby Lambert, Marie-Antoinette Voelckel, Ulrika Hosterey-Ugander, Heather Skirton. J Community Genet 2012
28
14

Hereditary ataxia and spastic paraplegia in Portugal: a population-based prevalence study.
Paula Coutinho, Luis Ruano, José L Loureiro, Vitor T Cruz, José Barros, Assunção Tuna, Clara Barbot, João Guimarães, Isabel Alonso, Isabel Silveira,[...]. JAMA Neurol 2013
66
14



Using a community of practice to develop standards of practice and education for genetic counsellors in Europe.
Heather Skirton, Christine Patch, Marie-Antoinette Voelckel. J Community Genet 2010
20
14

Non-syndromic sensorineural prelingual deafness: the importance of genetic counseling in demystifying parents' beliefs about the cause of their children's deafness.
Fidjy Rodrigues, Milena Paneque, Cláudia Reis, Margarida Venâncio, Jorge Sequeiros, Jorge Saraiva. J Genet Couns 2013
5
20


Indications for genetic referral: a guide for healthcare providers.
Beth A Pletcher, Helga V Toriello, Sarah J Noblin, Laurie H Seaver, Deborah A Driscoll, Robin L Bennett, Susan J Gross. Genet Med 2007
27
14

Portugal: the practice of medical genetics in Portugal. Portuguese Society of Human Genetics.
J M Saraiva, M R Pinto, C Monteiro, M R Lima, A Medeira, P Rendeiro. Genet Med 2001
2
50

Educating genetic counselors in Australia-developing a masters program.
Margaret Sahhar, Jan Hodgson, Samantha Wake. J Genet Couns 2013
9
14

Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling.
Alvaro Mendes, Raquel Chiquelho, Teresa Almeida Santos, Liliana Sousa. J Community Genet 2010
14
14

The importance of the general practitioner as an information source for patients with hereditary haemochromatosis.
Emerência Teixeira, Júlio Borlido-Santos, Pierre Brissot, Barbara Butzeck, Françoise Courtois, Robert W Evans, Janet Fernau, João Arriscado Nunes, Margaret Mullett, Milena Paneque,[...]. Patient Educ Couns 2014
7
14


THEMIS and PTPRK in celiac intestinal mucosa: coexpression in disease and after in vitro gliadin challenge.
Constanza Bondar, Leticia Plaza-Izurieta, Nora Fernandez-Jimenez, Iñaki Irastorza, Sebo Withoff, Cisca Wijmenga, Fernando Chirdo, Jose Ramon Bilbao. Eur J Hum Genet 2014
16
14

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
14

Motor decline in clinically presymptomatic spinocerebellar ataxia type 2 gene carriers.
Luis Velázquez-Perez, Rosalinda Díaz, Ruth Pérez-González, Nalia Canales, Roberto Rodríguez-Labrada, Jacquelín Medrano, Gilberto Sánchez, Luis Almaguer-Mederos, Cira Torres, Juan Fernandez-Ruiz. PLoS One 2009
18
14

Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis.
Hussein Daoud, Véronique Belzil, Sandra Martins, Mike Sabbagh, Pierre Provencher, Lucette Lacomblez, Vincent Meininger, William Camu, Nicolas Dupré, Patrick A Dion,[...]. Arch Neurol 2011
61
14

Psychosocial issues in genetic testing for familial adenomatous polyposis: a review of the literature.
K F L Douma, N K Aaronson, H F A Vasen, E M A Bleiker. Psychooncology 2008
32
14

EMQN Best Practice Guidelines for molecular genetic testing of SCAs.
Jorge Sequeiros, Joanne Martindale, Sara Seneca, Paola Giunti, Outi Kämäräinen, Victor Volpini, Helga Weirich, Kyproula Christodoulou, Nazli Bazak, Richard Sinke,[...]. Eur J Hum Genet 2010
25
14

Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles.
José Miguel Laffita-Mesa, Luis C Velázquez-Pérez, Nieves Santos Falcón, Tania Cruz-Mariño, Yanetza González Zaldívar, Yaimee Vázquez Mojena, Dennis Almaguer-Gotay, Luis Enrique Almaguer Mederos, Roberto Rodríguez Labrada. Eur J Hum Genet 2012
32
14

The use of genetic testing in hereditary colorectal cancer syndromes: genetic testing in HNPCC, (A)FAP and MAP.
D Ramsoekh, M E van Leerdam, C M J Tops, D Dooijes, E W Steyerberg, E J Kuipers, A Wagner. Clin Genet 2007
26
14

De novo mutations in ataxin-2 gene and ALS risk.
José Miguel Laffita-Mesa, Jorge Michel Rodríguez Pupo, Raciel Moreno Sera, Yaimee Vázquez Mojena, Vivian Kourí, Leonides Laguna-Salvia, Michael Martínez-Godales, José A Valdevila Figueira, Peter O Bauer, Roberto Rodríguez-Labrada,[...]. PLoS One 2013
18
14

Prenatal testing for Huntington's disease: a European collaborative study.
Sheila A Simpson, Moniek W Zoeteweij, Kurt Nys, Peter Harper, Alexandra Dürr, Gioia Jacopini, Christos Yapijakis, Gerry Evers-Kiebooms. Eur J Hum Genet 2002
30
14

Lessons from predictive testing for Huntington disease: 25 years on.
Alice K Hawkins, Anita Ho, Michael R Hayden. J Med Genet 2011
12
14

Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.
S Creighton, E W Almqvist, D MacGregor, B Fernandez, H Hogg, J Beis, J P Welch, C Riddell, R Lokkesmoe, M Khalifa,[...]. Clin Genet 2003
114
14

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
14

Comprehensive study of early features in spinocerebellar ataxia 2: delineating the prodromal stage of the disease.
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Edilia M Cruz-Rivas, Juan Fernández-Ruiz, Israel Vaca-Palomares, Jandy Lilia-Campins, Bulmaro Cisneros, Arnoy Peña-Acosta, Yaimeé Vázquez-Mojena, Rosalinda Diaz,[...]. Cerebellum 2014
39
14

Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2.
L Velázquez-Pérez, C Seifried, M Abele, F Wirjatijasa, R Rodríguez-Labrada, N Santos-Falcón, G Sánchez-Cruz, L Almaguer-Mederos, R Tejeda, N Canales-Ochoa,[...]. Clin Neurophysiol 2009
54
14

Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias.
Jorge Sequeiros, Sara Seneca, Joanne Martindale. Eur J Hum Genet 2010
48
14


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.