A citation-based method for searching scientific literature

Deborah Mascalzoni, Edward S Dove, Yaffa Rubinstein, Hugh J S Dawkins, Anna Kole, Pauline McCormack, Simon Woods, Olaf Riess, Franz Schaefer, Hanns Lochmüller, Bartha M Knoppers, Mats Hansson. Eur J Hum Genet 2015
Times Cited: 73







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



Times Cited
  Times     Co-cited
Similarity


RD-Connect: an integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research.
Rachel Thompson, Louise Johnston, Domenica Taruscio, Lucia Monaco, Christophe Béroud, Ivo G Gut, Mats G Hansson, Peter-Bram A 't Hoen, George P Patrinos, Hugh Dawkins,[...]. J Gen Intern Med 2014
101
23


The Matchmaker Exchange: a platform for rare disease gene discovery.
Anthony A Philippakis, Danielle R Azzariti, Sergi Beltran, Anthony J Brookes, Catherine A Brownstein, Michael Brudno, Han G Brunner, Orion J Buske, Knox Carey, Cassie Doll,[...]. Hum Mutat 2015
228
15

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
213
13

The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases.
Marina Mora, Corrado Angelini, Fabrizia Bignami, Anne-Mary Bodin, Marco Crimi, Jeanne-Hélène Di Donato, Alex Felice, Cécile Jaeger, Veronika Karcagi, Yann LeCam,[...]. Eur J Hum Genet 2015
37
27

Towards a data sharing Code of Conduct for international genomic research.
Bartha Maria Knoppers, Jennifer R Harris, Anne Marie Tassé, Isabelle Budin-Ljøsne, Jane Kaye, Mylène Deschênes, Ma'n H Zawati. Genome Med 2011
65
13

The Human Phenotype Ontology in 2017.
Sebastian Köhler, Nicole A Vasilevsky, Mark Engelstad, Erin Foster, Julie McMurry, Ségolène Aymé, Gareth Baynam, Susan M Bello, Cornelius F Boerkoel, Kym M Boycott,[...]. Nucleic Acids Res 2017
398
12

'IRDiRC Recognized Resources': a new mechanism to support scientists to conduct efficient, high-quality research for rare diseases.
Hanns Lochmüller, Yann Le Cam, Anneliene H Jonker, Lilian Pl Lau, Gareth Baynam, Petra Kaufmann, Paul Lasko, Hugh Js Dawkins, Christopher P Austin, Kym M Boycott. Eur J Hum Genet 2017
24
37

The FAIR Guiding Principles for scientific data management and stewardship.
Mark D Wilkinson, Michel Dumontier, I Jsbrand Jan Aalbersberg, Gabrielle Appleton, Myles Axton, Arie Baak, Niklas Blomberg, Jan-Willem Boiten, Luiz Bonino da Silva Santos, Philip E Bourne,[...]. Sci Data 2016
12

Improving the informed consent process in international collaborative rare disease research: effective consent for effective research.
Sabina Gainotti, Cathy Turner, Simon Woods, Anna Kole, Pauline McCormack, Hanns Lochmüller, Olaf Riess, Volker Straub, Manuel Posada, Domenica Taruscio,[...]. Eur J Hum Genet 2016
25
32

The TREAT-NMD Duchenne muscular dystrophy registries: conception, design, and utilization by industry and academia.
Catherine L Bladen, Karen Rafferty, Volker Straub, Soledad Monges, Angélica Moresco, Hugh Dawkins, Anna Roy, Teodora Chamova, Velina Guergueltcheva, Lawrence Korngut,[...]. Hum Mutat 2013
74
9

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
Sebastian Köhler, Sandra C Doelken, Christopher J Mungall, Sebastian Bauer, Helen V Firth, Isabelle Bailleul-Forestier, Graeme C M Black, Danielle L Brown, Michael Brudno, Jennifer Campbell,[...]. Nucleic Acids Res 2014
440
9

A human rights approach to an international code of conduct for genomic and clinical data sharing.
Bartha M Knoppers, Jennifer R Harris, Isabelle Budin-Ljøsne, Edward S Dove. Hum Genet 2014
47
14

The challenge for a European network of biobanks for rare diseases taken up by RD-Connect.
Lucia Monaco, Marco Crimi, Chiuhui Mary Wang. Pathobiology 2014
15
46

Toward a roadmap in global biobanking for health.
Jennifer R Harris, Paul Burton, Bartha Maria Knoppers, Klaus Lindpaintner, Marianna Bledsoe, Anthony J Brookes, Isabelle Budin-Ljøsne, Rex Chisholm, David Cox, Mylène Deschênes,[...]. Eur J Hum Genet 2012
80
8

Representation of rare diseases in health information systems: the Orphanet approach to serve a wide range of end users.
Ana Rath, Annie Olry, Ferdinand Dhombres, Maja Miličić Brandt, Bruno Urbero, Segolene Ayme. Hum Mutat 2012
176
8


Developing a guideline to standardize the citation of bioresources in journal articles (CoBRA).
Elena Bravo, Alessia Calzolari, Paola De Castro, Laurence Mabile, Federica Napolitani, Anna Maria Rossi, Anne Cambon-Thomsen. BMC Med 2015
27
22

A solidarity-based approach to the governance of research biobanks.
Barbara Prainsack, Alena Buyx. Med Law Rev 2013
39
12

Quantifying the use of bioresources for promoting their sharing in scientific research.
Laurence Mabile, Raymond Dalgleish, Gudmundur A Thorisson, Mylène Deschênes, Robert Hewitt, Jane Carpenter, Elena Bravo, Mirella Filocamo, Pierre Antoine Gourraud, Jennifer R Harris,[...]. Gigascience 2013
31
16

PhenomeCentral: a portal for phenotypic and genotypic matchmaking of patients with rare genetic diseases.
Orion J Buske, Marta Girdea, Sergiu Dumitriu, Bailey Gallinger, Taila Hartley, Heather Trang, Andriy Misyura, Tal Friedman, Chandree Beaulieu, William P Bone,[...]. Hum Mutat 2015
72
6

FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project.
Chandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, Mark E Samuels, Bridget A Fernandez, Francois P Bernier, Michael Brudno, Bartha Knoppers, Janet Marcadier, David Dyment,[...]. Am J Hum Genet 2014
149
6

'Access arrangements' for biobanks: a fine line between facilitating and hindering collaboration.
S Fortin, S Pathmasiri, R Grintuch, M Deschênes. Public Health Genomics 2011
27
18

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
143
6

PhenoTips: patient phenotyping software for clinical and research use.
Marta Girdea, Sergiu Dumitriu, Marc Fiume, Sarah Bowdin, Kym M Boycott, Sébastien Chénier, David Chitayat, Hanna Faghfoury, M Stephen Meyn, Peter N Ray,[...]. Hum Mutat 2013
137
6

From the principles of genomic data sharing to the practices of data access committees.
Mahsa Shabani, Bartha Maria Knoppers, Pascal Borry. EMBO Mol Med 2015
24
20

'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research.
Pauline McCormack, Anna Kole, Sabina Gainotti, Deborah Mascalzoni, Caron Molster, Hanns Lochmüller, Simon Woods. Eur J Hum Genet 2016
35
14

International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.
Kym M Boycott, Ana Rath, Jessica X Chong, Taila Hartley, Fowzan S Alkuraya, Gareth Baynam, Anthony J Brookes, Michael Brudno, Angel Carracedo, Johan T den Dunnen,[...]. Am J Hum Genet 2017
152
6

The International Rare Diseases Research Consortium: Policies and Guidelines to maximize impact.
Hanns Lochmüller, Josep Torrent I Farnell, Yann Le Cam, Anneliene H Jonker, Lilian Pl Lau, Gareth Baynam, Petra Kaufmann, Hugh Js Dawkins, Paul Lasko, Christopher P Austin,[...]. Eur J Hum Genet 2017
32
15

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
5

Data sharing by scientists: practices and perceptions.
Carol Tenopir, Suzie Allard, Kimberly Douglass, Arsev Umur Aydinoglu, Lei Wu, Eleanor Read, Maribeth Manoff, Mike Frame. PLoS One 2011
177
5



From patients to partners: participant-centric initiatives in biomedical research.
Jane Kaye, Liam Curren, Nick Anderson, Kelly Edwards, Stephanie M Fullerton, Nadja Kanellopoulou, David Lund, Daniel G MacArthur, Deborah Mascalzoni, James Shepherd,[...]. Nat Rev Genet 2012
159
5

DataSHIELD: taking the analysis to the data, not the data to the analysis.
Amadou Gaye, Yannick Marcon, Julia Isaeva, Philippe LaFlamme, Andrew Turner, Elinor M Jones, Joel Minion, Andrew W Boyd, Christopher J Newby, Marja-Liisa Nuotio,[...]. Int J Epidemiol 2014
77
5

A review of the barriers to sharing in biobanking.
Flora Colledge, Bernice Elger, Heidi C Howard. Biopreserv Biobank 2013
12
33

Custodianship as an ethical framework for biospecimen-based research.
Rihab Yassin, Nicole Lockhart, Mariana González del Riego, Karen Pitt, Jeffrey W Thomas, Linda Weiss, Carolyn Compton. Cancer Epidemiol Biomarkers Prev 2010
33
12

The role of a bioresource research impact factor as an incentive to share human bioresources.
Anne Cambon-Thomsen, Gudmundur A Thorisson, Laurence Mabile. Nat Genet 2011
42
9

Rare-disease genetics in the era of next-generation sequencing: discovery to translation.
Kym M Boycott, Megan R Vanstone, Dennis E Bulman, Alex E MacKenzie. Nat Rev Genet 2013
425
5

Undiagnosed Diseases Network International (UDNI): White paper for global actions to meet patient needs.
Domenica Taruscio, Stephen C Groft, Helene Cederroth, Béla Melegh, Paul Lasko, Kenjiro Kosaki, Gareth Baynam, Alexa McCray, William A Gahl. Mol Genet Metab 2015
40
10

Future of Rare Diseases Research 2017-2027: An IRDiRC Perspective.
Christopher P Austin, Christine M Cutillo, Lilian P L Lau, Anneliene H Jonker, Ana Rath, Daria Julkowska, David Thomson, Sharon F Terry, Béatrice de Montleau, Diego Ardigò,[...]. Clin Transl Sci 2018
68
5

Samples and data accessibility in research biobanks: an explorative survey.
Marco Capocasa, Paolo Anagnostou, Flavio D'Abramo, Giulia Matteucci, Valentina Dominici, Giovanni Destro Bisol, Fabrizio Rufo. PeerJ 2016
13
30

The role of biobanking in rare diseases: European consensus expert group report.
Hanns Lochmüller, Ségolène Aymé, Francesca Pampinella, Béla Melegh, Klaus A Kuhn, Stylianos E Antonarakis, Thomas Meitinger. Biopreserv Biobank 2009
14
21

Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases.
Mirella Filocamo, Chiara Baldo, Stefano Goldwurm, Alessandra Renieri, Corrado Angelini, Maurizio Moggio, Marina Mora, Giuseppe Merla, Luisa Politano, Barbara Garavaglia,[...]. Orphanet J Rare Dis 2013
23
13

Broad consent versus dynamic consent in biobank research: is passive participation an ethical problem?
Kristin Solum Steinsbekk, Bjørn Kåre Myskja, Berge Solberg. Eur J Hum Genet 2013
120
4

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
53
5

Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational.
Pauline McCormack, Simon Woods, Annemieke Aartsma-Rus, Lynn Hagger, Agnes Herczegfalvi, Emma Heslop, Joseph Irwin, Janbernd Kirschner, Patrick Moeschen, Francesco Muntoni,[...]. PLoS Curr 2013
13
23

Publics and biobanks: Pan-European diversity and the challenge of responsible innovation.
George Gaskell, Herbert Gottweis, Johannes Starkbaum, Monica M Gerber, Jacqueline Broerse, Ursula Gottweis, Abbi Hobbs, Ilpo Helén, Maria Paschou, Karoliina Snell,[...]. Eur J Hum Genet 2013
51
5

Data sharing in large research consortia: experiences and recommendations from ENGAGE.
Isabelle Budin-Ljøsne, Julia Isaeva, Bartha Maria Knoppers, Anne Marie Tassé, Huei-yi Shen, Mark I McCarthy, Jennifer R Harris. Eur J Hum Genet 2014
34
8

The European Genome-phenome Archive of human data consented for biomedical research.
Ilkka Lappalainen, Jeff Almeida-King, Vasudev Kumanduri, Alexander Senf, John Dylan Spalding, Saif Ur-Rehman, Gary Saunders, Jag Kandasamy, Mario Caccamo, Rasko Leinonen,[...]. Nat Genet 2015
171
4


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.