A citation-based method for searching scientific literature

Seth J Rotz, Eric Kodish. Hematology Am Soc Hematol Educ Program 2018
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am J Hum Genet 2015
220
50

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
50

Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.
Eva Leinøe, Eva Zetterberg, Savvas Kinalis, Olga Østrup, Peter Kampmann, Eva Norström, Nadine Andersson, Jenny Klintman, Klaus Qvortrup, Finn Cilius Nielsen,[...]. Br J Haematol 2017
36
25

Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.
Kate Downes, Karyn Megy, Daniel Duarte, Minka Vries, Johanna Gebhart, Stefanie Hofer, Olga Shamardina, Sri V V Deevi, Jonathan Stephens, Rutendo Mapeta,[...]. Blood 2019
70
25

The 2017 international classification of the Ehlers-Danlos syndromes.
Fransiska Malfait, Clair Francomano, Peter Byers, John Belmont, Britta Berglund, James Black, Lara Bloom, Jessica M Bowen, Angela F Brady, Nigel P Burrows,[...]. Am J Med Genet C Semin Med Genet 2017
532
25


Developmental hemostasis: A lifespan from neonates and pregnancy to the young and elderly adult in a European white population.
Ulrike Nowak-Göttl, Verena Limperger, Gili Kenet, Frauke Degenhardt, Roman Arlt, Justus Domschikowski, Hartmut Clausnizer, Jürgen Liebsch, Ralf Junker, Dagmar Steppat. Blood Cells Mol Dis 2017
18
25




Recommendations for the Standardization of Light Transmission Aggregometry: A Consensus of the Working Party from the Platelet Physiology Subcommittee of SSC/ISTH.
M Cattaneo, C Cerletti, P Harrison, C P M Hayward, D Kenny, D Nugent, P Nurden, A K Rao, A H Schmaier, S P Watson,[...]. J Thromb Haemost 2013
265
25

Experiences of predictive testing in young people at risk of Huntington's disease, familial cardiomyopathy or hereditary breast and ovarian cancer.
Rhona MacLeod, Anna Beach, Sasha Henriques, Jasmin Knopp, Katie Nelson, Lauren Kerzin-Storrar. Eur J Hum Genet 2014
26
25

Diagnosis of inherited bleeding disorders in the genomic era.
Suthesh Sivapalaratnam, Janine Collins, Keith Gomez. Br J Haematol 2017
34
25

Outcome of an enhanced diagnostic pipeline for patients suspected of inherited thrombocytopenia.
Eva Leinøe, Migle Gabrielaite, Olga Østrup, Eva Funding, Andreas Greinacher, Sisse R Ostrowski, Eva Zetterberg, Maria Rossing. Br J Haematol 2019
10
25

Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding.
Marcus Fager Ferrari, Eva Leinoe, Maria Rossing, Eva Norström, Karin Strandberg, Tobias Steen Sejersen, Klaus Qvortrup, Eva Zetterberg. Platelets 2018
8
25

MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.
Alessandro Pecci, Catherine Klersy, Paolo Gresele, Kieran J D Lee, Daniela De Rocco, Valeria Bozzi, Giovanna Russo, Paula G Heller, Giuseppe Loffredo, Matthias Ballmaier,[...]. Hum Mutat 2014
108
25




Collagen-mediated hemostasis.
T Manon-Jensen, N G Kjeld, M A Karsdal. J Thromb Haemost 2016
50
25

Aggregometry in the settings of thrombocytopenia, thrombocytosis and antiplatelet therapy.
GianMarco Podda, Mariangela Scavone, Eti Alessandra Femia, Marco Cattaneo. Platelets 2018
4
25




Severity and Features of Epistaxis in Children with a Mucocutaneous Bleeding Disorder.
Eva Stokhuijzen, Catherine I Segbefia, Tina T Biss, Dewi S Clark, Paula D James, Jim Riddel, Victor S Blanchette, Margaret L Rand. J Pediatr 2018
3
33

Hypermobility and Musculoskeletal Pain in Adolescents.
Susan L Morris, Peter B O'Sullivan, Kevin J Murray, Natasha Bear, Beth Hands, Anne J Smith. J Pediatr 2017
19
25

Quantitation of bleeding symptoms in children with von Willebrand disease: use of a standardized pediatric bleeding questionnaire.
T T Biss, V S Blanchette, D S Clark, M Bowman, C D Wakefield, M Silva, D Lillicrap, P D James, M L Rand. J Thromb Haemost 2010
85
25

Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders.
A Greinacher, A Pecci, S Kunishima, K Althaus, P Nurden, C L Balduini, T Bakchoul. J Thromb Haemost 2017
36
25

Curated disease-causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH.
Karyn Megy, Kate Downes, Ilenia Simeoni, Loredana Bury, Joannella Morales, Rutendo Mapeta, Daniel B Bellissimo, Paul F Bray, Anne C Goodeve, Paolo Gresele,[...]. J Thromb Haemost 2019
32
25

Diagnostic laboratory standardization and validation of platelet transmission electron microscopy.
Dong Chen, Cindy B Uhl, Sandra C Bryant, Marcy Krumwiede, Ryan L Barness, Mary C Olson, Susan C Gossman, Sibel Erdogan Damgard, Scott I Gamb, Lisa A Cummins,[...]. Platelets 2018
14
25

Hemostatic abnormalities in patients with Ehlers-Danlos syndrome.
A Artoni, A Bassotti, M Abbattista, B Marinelli, A Lecchi, F Gianniello, M Clerici, P Bucciarelli, S La Marca, F Peyvandi,[...]. J Thromb Haemost 2018
9
25


A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
25

A simplified flow cytometric method for detection of inherited platelet disorders-A comparison to the gold standard light transmission aggregometry.
Kristoffer Navred, Myriam Martin, Lina Ekdahl, Eva Zetterberg, Nadine Gretenkort Andersson, Karin Strandberg, Eva Norstrom. PLoS One 2019
7
25


Inherited platelet disorders: toward DNA-based diagnosis.
Claire Lentaigne, Kathleen Freson, Michael A Laffan, Ernest Turro, Willem H Ouwehand. Blood 2016
83
25


Incidental copy-number variants identified by routine genome testing in a clinical population.
Philip M Boone, Zachry T Soens, Ian M Campbell, Pawel Stankiewicz, Sau Wai Cheung, Ankita Patel, Arthur L Beaudet, Sharon E Plon, Chad A Shaw, Amy L McGuire,[...]. Genet Med 2013
31
25

Speaking genomics to parents offered germline testing for cancer predisposition: Use of a 2-visit consent model.
Liza-Marie Johnson, April D Sykes, Zhaohua Lu, Jessica M Valdez, Jami Gattuso, Elsie Gerhardt, Kayla V Hamilton, Lynn W Harrison, Stacy J Hines-Dowell, Niki Jurbergs,[...]. Cancer 2019
7
25

Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations.
Jennifer A Oberg, Julia L Glade Bender, Maria Luisa Sulis, Danielle Pendrick, Anthony N Sireci, Susan J Hsiao, Andrew T Turk, Filemon S Dela Cruz, Hanina Hibshoosh, Helen Remotti,[...]. Genome Med 2016
82
25


Development and validation of a Breast Cancer Genetic Counseling Knowledge Questionnaire.
Joel Erblich, Karen Brown, Youngmee Kim, Heiddis B Valdimarsdottir, Barbara E Livingston, Dana H Bovbjerg. Patient Educ Couns 2005
50
25

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
D Williams Parsons, Angshumoy Roy, Yaping Yang, Tao Wang, Sarah Scollon, Katie Bergstrom, Robin A Kerstein, Stephanie Gutierrez, Andrea K Petersen, Abhishek Bavle,[...]. JAMA Oncol 2016
232
25

Therapeutic implications of germline genetic findings in cancer.
Subotheni Thavaneswaran, Emma Rath, Kathy Tucker, Anthony M Joshua, Dominique Hess, Mark Pinese, Mandy L Ballinger, David M Thomas. Nat Rev Clin Oncol 2019
21
25

Risk perception, worry and satisfaction related to genetic counseling for hereditary cancer.
Cathrine Bjorvatn, Geir Egil Eide, Berit Rokne Hanestad, Nina Øyen, Odd E Havik, Anniken Carlsson, Gunilla Berglund. J Genet Couns 2007
44
25

Integrating genetic counseling and testing in the pediatric oncology setting: Parental attitudes and influencing factors.
Lauren R Desrosiers, Emily Quinn, Stuart Cramer, Whitney Dobek. Pediatr Blood Cancer 2019
4
25

Regular surveillance for Li-Fraumeni Syndrome: advice, adherence and perceived benefits.
C R M Lammens, E M A Bleiker, N K Aaronson, A Wagner, R H Sijmons, M G E M Ausems, A H J T Vriends, M W G Ruijs, T A M van Os, L Spruijt,[...]. Fam Cancer 2010
41
25

Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth.
Rajen J Mody, Yi-Mi Wu, Robert J Lonigro, Xuhong Cao, Sameek Roychowdhury, Pankaj Vats, Kevin M Frank, John R Prensner, Irfan Asangani, Nallasivam Palanisamy,[...]. JAMA 2015
227
25

Genetic Counselor Recommendations for Cancer Predisposition Evaluation and Surveillance in the Pediatric Oncology Patient.
Harriet Druker, Kristin Zelley, Rose B McGee, Sarah R Scollon, Wendy K Kohlmann, Katherine A Schneider, Kami Wolfe Schneider. Clin Cancer Res 2017
50
25



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.