A citation-based method for searching scientific literature

Alison M Elliott. Cold Spring Harb Perspect Med 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Internet Use by Parents of Children With Rare Conditions: Findings From a Study on Parents' Web Information Needs.
Honor Nicholl, Catherine Tracey, Thelma Begley, Carole King, Aileen M Lynch. J Med Internet Res 2017
43
66

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
66

Diagnosis of Cystic Fibrosis in Screened Populations.
Philip M Farrell, Terry B White, Michelle S Howenstine, Anne Munck, Richard B Parad, Margaret Rosenfeld, Olaf Sommerburg, Frank J Accurso, Jane C Davies, Michael J Rock,[...]. J Pediatr 2017
48
33

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17
33

The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine.
Katie Stoll, Shobana Kubendran, Stephanie A Cohen. Am J Med Genet C Semin Med Genet 2018
64
33

Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice.
Setareh Ashtiani, Nancy Makela, Prescilla Carrion, Jehannine Austin. Am J Med Genet A 2014
20
33

Cost-effectiveness analysis of lumacaftor and ivacaftor combination for the treatment of patients with cystic fibrosis in the United States.
Dolly Sharma, Shan Xing, Yu-Ting Hung, Rachel N Caskey, Maria L Dowell, Daniel R Touchette. Orphanet J Rare Dis 2018
6
33

The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of Services.
Benjamin M Helm, Samantha L Freeze, Katherine G Spoonamore, Stephanie M Ware, Mark D Ayers, Adam C Kean. J Genet Couns 2018
7
33

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
842
33

Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study.
Margaret Rosenfeld, Claire E Wainwright, Mark Higgins, Linda T Wang, Charlotte McKee, Daniel Campbell, Simon Tian, Jennifer Schneider, Steve Cunningham, Jane C Davies. Lancet Respir Med 2018
95
33

Parental understanding of newborn screening for cystic fibrosis after a negative sweat-test.
Colleen Walsh Lang, Susanna A McColley, Lucille A Lester, Lainie Friedman Ross. Pediatrics 2011
23
33

Population-based carrier screening for cystic fibrosis: a systematic review of 23 years of research.
Liane Ioannou, Belinda J McClaren, John Massie, Sharon Lewis, Sylvia A Metcalfe, Laura Forrest, Martin B Delatycki. Genet Med 2014
44
33

A Case for Inclusion of Genetic Counselors in Cardiac Care.
Patricia Arscott, Colleen Caleshu, Katrina Kotzer, Sarah Kreykes, Teresa Kruisselbrink, Kate Orland, Christina Rigelsky, Emily Smith, Katherine Spoonamore, Joy Larsen Haidle,[...]. Cardiol Rev 2016
21
33

Sex Education and Intellectual Disability: Practices and Insight from Pediatric Genetic Counselors.
Carly Murphy, Sharyn Lincoln, Stephanie Meredith, Elizabeth M Cross, David Rintell. J Genet Couns 2016
5
33

Elaboration of the Reciprocal-Engagement Model of Genetic Counseling Practice: a Qualitative Investigation of Goals and Strategies.
Krista Redlinger-Grosse, Patricia McCarthy Veach, Bonnie S LeRoy, Heather Zierhut. J Genet Couns 2017
10
33



Is cystic fibrosis genetic medicine's canary?
Susan Lindee, Rebecca Mueller. Perspect Biol Med 2011
4
33

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene.
Patrick R Sosnay, Karen R Siklosi, Fredrick Van Goor, Kyle Kaniecki, Haihui Yu, Neeraj Sharma, Anabela S Ramalho, Margarida D Amaral, Ruslan Dorfman, Julian Zielenski,[...]. Nat Genet 2013
361
33

Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening.
Roman Shraga, Sarah Yarnall, Sonya Elango, Arun Manoharan, Sally Ann Rodriguez, Sara L Bristow, Neha Kumar, Mohammad Niknazar, David Hoffman, Shahin Ghadir,[...]. BMC Genet 2017
13
33

Adolescents' preferences regarding disclosure of incidental findings in genomic sequencing that are not medically actionable in childhood.
Sophia B Hufnagel, Lisa J Martin, Amy Cassedy, Robert J Hopkin, Armand H Matheny Antommaria. Am J Med Genet A 2016
18
33

Secondary findings in 421 whole exome-sequenced Chinese children.
Wen Chen, Wenke Li, Yi Ma, Yujing Zhang, Bianmei Han, Xuewen Liu, Kun Zhao, Meixian Zhang, Jie Mi, Yuanyuan Fu,[...]. Hum Genomics 2018
4
33

Genetic counseling in a busy pediatric metabolic practice.
Jessica N Hartley, Cheryl R Greenberg, Aizeddin A Mhanni. J Genet Couns 2011
7
33

Experience with genetic counseling: the adolescent perspective.
Amanda Pichini, Cheryl Shuman, Karen Sappleton, Miriam Kaufman, David Chitayat, Riyana Babul-Hirji. J Genet Couns 2016
10
33

Medical management adherence as an outcome of genetic counseling in a pediatric setting.
Sarah Rutherford, Xue Zhang, Carrie Atzinger, Jennifer Ruschman, Melanie F Myers. Genet Med 2014
15
33


Breaking bad news in genetic counseling-problems and communication tools.
Magdalena M Witt, Katarzyna A Jankowska. J Appl Genet 2018
9
33

Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del.
Jennifer L Taylor-Cousar, Anne Munck, Edward F McKone, Cornelis K van der Ent, Alexander Moeller, Christopher Simard, Linda T Wang, Edward P Ingenito, Charlotte McKee, Yimeng Lu,[...]. N Engl J Med 2017
335
33

A tailored approach to family-centered genetic counseling for cystic fibrosis newborn screening: the Wisconsin model.
Audrey Tluczek, Christina Zaleski, Dania Stachiw-Hietpas, Peggy Modaff, Craig R Adamski, Megan R Nelson, Catherine A Reiser, Sumedha Ghate, Kevin D Josephson. J Genet Couns 2011
15
33

Cystic Fibrosis: The Dawn of a New Therapeutic Era.
Sonya L Heltshe, Jonathan Cogen, Kathleen J Ramos, Christopher H Goss. Am J Respir Crit Care Med 2017
17
33

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
33

Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis.
R G Crystal, N G McElvaney, M A Rosenfeld, C S Chu, A Mastrangeli, J G Hay, S L Brody, H A Jaffe, N T Eissa, C Danel. Nat Genet 1994
715
33

Current and emerging comorbidities in cystic fibrosis.
Nicola J Ronan, Joseph Stuart Elborn, Barry J Plant. Presse Med 2017
28
33



Changing trends in carrier screening for genetic disease in the United States.
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat Diagn 2015
45
33


Benign and Deleterious Cystic Fibrosis Transmembrane Conductance Regulator Mutations Identified by Sequencing in Positive Cystic Fibrosis Newborn Screen Children from California.
Danieli B Salinas, Patrick R Sosnay, Colleen Azen, Suzanne Young, Karen S Raraigh, Thomas G Keens, Martin Kharrazi. PLoS One 2016
20
33

Attitudes Toward Discussing Approved and Investigational Treatments for Cystic Fibrosis in Prenatal Genetic Counseling Practice.
Caroline Rung Elsas, Elinor Langfelder Schwind, Laura Hercher, Michael J Smith, Kara Gardner Young. J Genet Couns 2017
3
33

Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
Linyan Meng, Mohan Pammi, Anirudh Saronwala, Pilar Magoulas, Andrew Ray Ghazi, Francesco Vetrini, Jing Zhang, Weimin He, Avinash V Dharmadhikari, Chunjing Qu,[...]. JAMA Pediatr 2017
189
33


Long-term evaluation of genetic counseling following false-positive newborn screen for cystic fibrosis.
Laura Cavanagh, Cecilia J Compton, Audrey Tluczek, Roger L Brown, Philip M Farrell. J Genet Couns 2010
24
33

Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.
Galen Joseph, Flavia Chen, Julie Harris-Wai, Jennifer M Puck, Charlotte Young, Barbara A Koenig. Pediatrics 2016
21
33

Outcomes of infants with indeterminate diagnosis detected by cystic fibrosis newborn screening.
Clement L Ren, Aliza K Fink, Kristofer Petren, Drucy S Borowitz, Susanna A McColley, Don B Sanders, Margaret Rosenfeld, Bruce C Marshall. Pediatrics 2015
55
33

Mandatory versus voluntary consent for newborn screening?
Lainie Friedman Ross. Kennedy Inst Ethics J 2010
46
33

Advances in therapy for spinal muscular atrophy: promises and challenges.
Ewout J N Groen, Kevin Talbot, Thomas H Gillingwater. Nat Rev Neurol 2018
99
33

Communication challenges for nongeneticist physicians relaying clinical genomic results.
Nonie S Arora, J Kelly Davis, Christine Kirby, Amy L McGuire, Robert C Green, J S Blumenthal-Barby, Peter A Ubel. Per Med 2016
19
33

Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis.
Clement L Ren, Drucy S Borowitz, Tanja Gonska, Michelle S Howenstine, Hara Levy, John Massie, Carlos Milla, Anne Munck, Kevin W Southern. J Pediatr 2017
55
33

Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases.
Tessel Rigter, Lidewij Henneman, Jacqueline E W Broerse, Maggie Shepherd, Ignacio Blanco, Ulf Kristoffersson, Martina C Cornel. J Community Genet 2014
17
33



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.