A citation-based method for searching scientific literature

J Domínguez-Carral, J López-Pisón, A Macaya, M Bueno Campaña, M A García-Pérez, D Natera-de Benito. Eur J Med Genet 2017
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Use of genetic tests among neurologists and psychiatrists: knowledge, attitudes, behaviors, and needs for training.
Melissa Salm, Kristopher Abbate, Paul Appelbaum, Ruth Ottman, Wendy Chung, Karen Marder, Cheng-Shiun Leu, Roy Alcalay, Jill Goldman, Alexander Malik Curtis,[...]. J Genet Couns 2014
55
55


[Survey on the attitude toward genetic testing of neurologists certified by the Japanese Society of Neurology].
Kunihiro Yoshida, Takako Ohata, Kaori Muto, Atsushi Tsuchiya, Jinichi Sawada, Takanori Hazama, Shu-Ichi Ikeda, Tatsushi Toda. Rinsho Shinkeigaku 2013
4
50

Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review.
Katie E J Hann, Madeleine Freeman, Lindsay Fraser, Jo Waller, Saskia C Sanderson, Belinda Rahman, Lucy Side, Sue Gessler, Anne Lanceley. BMC Public Health 2017
83
22

Attitudes and practices among internists concerning genetic testing.
Robert Klitzman, Wendy Chung, Karen Marder, Anita Shanmugham, Lisa J Chin, Meredith Stark, Cheng-Shiun Leu, Paul S Appelbaum. J Genet Couns 2013
106
22

Knowledge, Attitudes, and Practice Regarding Genetic Testing and Genetic Counselors in Jordan: A Population-Based Survey.
Mamoun Ahram, Majd Soubani, Lana Abu Salem, Haneen Saker, Muayyad Ahmad. J Genet Couns 2015
9
22

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
50
22


Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
76
22

A systematic review of interventions to provide genetics education for primary care.
Milena Paneque, Daniela Turchetti, Leigh Jackson, Peter Lunt, Elisa Houwink, Heather Skirton. BMC Fam Pract 2016
40
22

Genetics professionals' perspectives on reporting incidental findings from clinical genome-wide sequencing.
Zoe Lohn, Shelin Adam, Patricia Birch, Anne Townsend, Jan Friedman. Am J Med Genet A 2013
43
11

Prevalence and quality of anxiety in patients with epilepsy.
Azad Maroufi, Payam Khomand, Somayeh Ahmadiani, Narges Shams Alizadeh, Fardin Gharibi. Epilepsy Behav 2014
12
11


Managing incidental genomic findings in clinical trials: fulfillment of the principle of justice.
Rafael Dal-Ré, Nicholas Katsanis, Sara Katsanis, Lisa S Parker, Carmen Ayuso. PLoS Med 2014
10
11

Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.
Samantha B Foley, Jonathan J Rios, Victoria E Mgbemena, Linda S Robinson, Heather L Hampel, Amanda E Toland, Leslie Durham, Theodora S Ross. EBioMedicine 2015
29
11

Mutations in HECW2 are associated with intellectual disability and epilepsy.
Jonatan Halvardson, Jin J Zhao, Ammar Zaghlool, Christian Wentzel, Patrik Georgii-Hemming, Else Månsson, Helena Ederth Sävmarker, Göran Brandberg, Cecilia Soussi Zander, Ann-Charlotte Thuresson,[...]. J Med Genet 2016
31
11

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases.
William A Gahl, Thomas C Markello, Camilo Toro, Karin Fuentes Fajardo, Murat Sincan, Fred Gill, Hannah Carlson-Donohoe, Andrea Gropman, Tyler Mark Pierson, Gretchen Golas,[...]. Genet Med 2012
180
11



Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular Pathology.
Madhuri Hegde, Sherri Bale, Pinar Bayrak-Toydemir, Jane Gibson, Linda Jo Bone Jeng, Loren Joseph, Jordan Laser, Ira M Lubin, Christine E Miller, Lainie F Ross,[...]. J Mol Diagn 2015
35
11


Whole-genome and whole-exome sequencing in neurological diseases.
Jia-Nee Foo, Jian-Jun Liu, Eng-King Tan. Nat Rev Neurol 2012
74
11


"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
120
11

Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.
Krishna R Veeramah, Laurel Johnstone, Tatiana M Karafet, Daniel Wolf, Ryan Sprissler, John Salogiannis, Asa Barth-Maron, Michael E Greenberg, Till Stuhlmann, Stefanie Weinert,[...]. Epilepsia 2013
173
11

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model.
Andrea H Németh, Alexandra C Kwasniewska, Stefano Lise, Ricardo Parolin Schnekenberg, Esther B E Becker, Katarzyna D Bera, Morag E Shanks, Lorna Gregory, David Buck, M Zameel Cader,[...]. Brain 2013
108
11

Reporting results from whole-genome and whole-exome sequencing in clinical practice: a proposal for Canada?
Ma'n H Zawati, David Parry, Adrian Thorogood, Minh Thu Nguyen, Kym M Boycott, David Rosenblatt, Bartha Maria Knoppers. J Med Genet 2014
21
11



Next generation sequencing in psychiatric research: what study participants need to know about research findings.
Ghislaine Mathieu, Iris Jaitovich Groisman, Beatrice Godard. Int J Neuropsychopharmacol 2013
10
11

The emerging agenda of stratified medicine in neurology.
Paul M Matthews, Paul Edison, Olivia C Geraghty, Michael R Johnson. Nat Rev Neurol 2014
15
11


Neurodevelopmental disorders and genetic testing: current approaches and future advances.
Elliott H Sherr, David J Michelson, Michael I Shevell, John B Moeschler, Andrea L Gropman, Stephen Ashwal. Ann Neurol 2013
15
11

Ethical issues in consumer genome sequencing: Use of consumers' samples and data.
Emilia Niemiec, Heidi Carmen Howard. Appl Transl Genom 2016
25
11

Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders.
Zhao Chen, Jun-Ling Wang, Bei-Sha Tang, Zhan-Fang Sun, Yu-Ting Shi, Lu Shen, Li-Fang Lei, Xiao-Ming Wei, Jing-Jing Xiao, Zheng-Mao Hu,[...]. Neurobiol Aging 2013
16
11

Legislation on direct-to-consumer genetic testing in seven European countries.
Pascal Borry, Rachel E van Hellemondt, Dominique Sprumont, Camilla Fittipaldi Duarte Jales, Emmanuelle Rial-Sebbag, Tade Matthias Spranger, Liam Curren, Jane Kaye, Herman Nys, Heidi Howard. Eur J Hum Genet 2012
71
11

The Future of Next-Generation Sequencing in Neurology.
Jean-Baptiste LePichon, Carol J Saunders, Sarah E Soden. JAMA Neurol 2015
5
20

Genetic risk perception and reproductive decision making among people with epilepsy.
Katherine L Helbig, Barbara A Bernhardt, Laura J Conway, Kathleen D Valverde, Ingo Helbig, Michael R Sperling. Epilepsia 2010
22
11

Next generation sequencing for neurological diseases: new hope or new hype?
M J Keogh, P F Chinnery. Clin Neurol Neurosurg 2013
16
11


Ethical considerations associated with clinical use of next-generation sequencing in children.
John D Lantos, Michael Artman, Stephen F Kingsmore. J Pediatr 2011
12
11


Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
238
11

Addressing gaps in physician education using personal genomic testing.
Richard R Sharp, Michael E Goldlust, Charis Eng. Genet Med 2011
20
11

Application of next-generation sequencing technologies in Neurology.
Teng Jiang, Meng-Shan Tan, Lan Tan, Jin-Tai Yu. Ann Transl Med 2014
30
11


22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
397
11

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
D A Driscoll, J Salvin, B Sellinger, M L Budarf, D M McDonald-McGinn, E H Zackai, B S Emanuel. J Med Genet 1993
404
11

Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
Chelsea Lowther, Daniele Merico, Gregory Costain, Jack Waserman, Kerry Boyd, Abdul Noor, Marsha Speevak, Dimitri J Stavropoulos, John Wei, Anath C Lionel,[...]. Genome Med 2017
14
11

Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders.
Rolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, Michael P Kwint, Irene M Janssen, Nicole de Leeuw, Helger G Yntema, Marcel R Nelen, Dorien Lugtenberg, Erik-Jan Kamsteeg,[...]. Genet Med 2017
75
11


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.