A citation-based method for searching scientific literature

Stephanie A Kraft, Devan Duenas, Benjamin S Wilfond, Katrina A B Goddard. Genet Med 2019
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity



ACMG position statement on prenatal/preconception expanded carrier screening.
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet. Med. 2013
104
58

Modeled Fetal Risk of Genetic Diseases Identified by Expanded Carrier Screening.
Imran S Haque, Gabriel A Lazarin, H Peter Kang, Eric A Evans, James D Goldberg, Ronald J Wapner. JAMA 2016
58
50

Responsible implementation of expanded carrier screening.
Lidewij Henneman, Pascal Borry, Davit Chokoshvili, Martina C Cornel, Carla G van El, Francesca Forzano, Alison Hall, Heidi C Howard, Sandra Janssens, Hülya Kayserili,[...]. Eur. J. Hum. Genet. 2016
85
50


Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen.
Kyle A Beauchamp, Katherine A Johansen Taber, Dale Muzzey. Genet. Med. 2019
14
41

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
41

Finding Middle Ground in Constructing a Clinically Useful Expanded Carrier Screening Panel.
Blair Stevens, Nevena Krstic, Malorie Jones, Lauren Murphy, Jennifer Hoskovec. Obstet Gynecol 2017
15
41

Expanded carrier screening for monogenic disorders: where are we now?
Davit Chokoshvili, Danya Vears, Pascal Borry. Prenat. Diagn. 2018
29
33

Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011
390
33


Clinical utility of expanded carrier screening: results-guided actionability and outcomes.
Katherine A Johansen Taber, Kyle A Beauchamp, Gabriel A Lazarin, Dale Muzzey, Aishwarya Arjunan, James D Goldberg. Genet. Med. 2019
12
25

Patient perspectives on the use of categories of conditions for decision making about genomic carrier screening results.
Stephanie A Kraft, Carmit K McMullen, Kathryn M Porter, Tia L Kauffman, James V Davis, Jennifer L Schneider, Katrina A B Goddard, Benjamin S Wilfond. Am. J. Med. Genet. A 2018
10
30

Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing.
Marian J Gilmore, Jennifer Schneider, James V Davis, Tia L Kauffman, Michael C Leo, Kellene Bergen, Jacob A Reiss, Patricia Himes, Elissa Morris, Carol Young,[...]. J Genet Couns 2017
17
25


Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel.
Michael S Watson, Garry R Cutting, Robert J Desnick, Deborah A Driscoll, Katherine Klinger, Michael Mennuti, Glenn E Palomaki, Bradley W Popovich, Victoria M Pratt, Elizabeth M Rohlfs,[...]. Genet. Med. 2004
255
25

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.
J R Riordan, J M Rommens, B Kerem, N Alon, R Rozmahel, Z Grzelczak, J Zielenski, S Lok, N Plavsic, J L Chou. Science 1989
25

Carrier screening for spinal muscular atrophy.
Thomas W Prior. Genet. Med. 2008
106
25


An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals.
Gabriel A Lazarin, Imran S Haque, Shivani Nazareth, Kevin Iori, A Scott Patterson, Jessica L Jacobson, John R Marshall, William K Seltzer, Pasquale Patrizio, Eric A Evans,[...]. Genet. Med. 2013
112
25

Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests.
Alison Dalton Archibald, Melanie Jane Smith, Trent Burgess, Katrina Louise Scarff, Justine Elliott, Clare Elizabeth Hunt, Zoe McDonald, Caitlin Barns-Jenkins, Chelsea Holt, Karina Sandoval,[...]. Genet. Med. 2018
33
25

Changing trends in carrier screening for genetic disease in the United States.
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat. Diagn. 2015
29
25

Validation for clinical use of, and initial clinical experience with, a novel approach to population-based carrier screening using high-throughput, next-generation DNA sequencing.
Stephanie Hallam, Heather Nelson, Valerie Greger, Cynthia Perreault-Micale, Jocelyn Davie, Nicole Faulkner, Dana Neitzel, Kristie Casey, Mark A Umbarger, Niru Chennagiri,[...]. J Mol Diagn 2014
23
25

Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange.  2014
22
16


Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant Identification.
Gregory J Hogan, Valentina S Vysotskaia, Kyle A Beauchamp, Stefanie Seisenberger, Peter V Grauman, Kevin R Haas, Sun Hae Hong, Diana Jeon, Shera Kash, Henry H Lai,[...]. Clin. Chem. 2018
15
16

Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels.
Gabriel A Lazarin, Felicia Hawthorne, Nicholas S Collins, Elizabeth A Platt, Eric A Evans, Imran S Haque. PLoS ONE 2014
36
16

Systematic design and comparison of expanded carrier screening panels.
Kyle A Beauchamp, Dale Muzzey, Kenny K Wong, Gregory J Hogan, Kambiz Karimi, Sophie I Candille, Nikita Mehta, Rebecca Mar-Heyming, K Eerik Kaseniit, H Peter Kang,[...]. Genet. Med. 2018
17
16

Expanded Carrier Screening.
Anthony R Gregg. Obstet. Gynecol. Clin. North Am. 2018
4
50

A data-driven evaluation of the size and content of expanded carrier screening panels.
Rotem Ben-Shachar, Ashley Svenson, James D Goldberg, Dale Muzzey. Genet. Med. 2019
10
20


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
33
16

"Is It Worth Knowing?" Focus Group Participants' Perceived Utility of Genomic Preconception Carrier Screening.
Jennifer L Schneider, Katrina A B Goddard, James Davis, Benjamin Wilfond, Tia L Kauffman, Jacob A Reiss, Marian Gilmore, Patricia Himes, Frances L Lynch, Michael C Leo,[...]. J Genet Couns 2016
27
16

Laboratory standards and guidelines for population-based cystic fibrosis carrier screening.
W W Grody, G R Cutting, K W Klinger, C S Richards, M S Watson, R J Desnick. Genet. Med. 2001
273
16

Growing complexity of (expanded) carrier screening: Direct-to-consumer, physician-mediated, and clinic-based offers.
Davit Chokoshvili, Danya F Vears, Pascal Borry. Best Pract Res Clin Obstet Gynaecol 2017
9
22


Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing.
Patricia Himes, Tia L Kauffman, Kristin R Muessig, Laura M Amendola, Jonathan S Berg, Michael O Dorschner, Marian Gilmore, Deborah A Nickerson, Jacob A Reiss, C Sue Richards,[...]. Genet. Med. 2017
19
16

Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.
Sumit Punj, Yassmine Akkari, Jennifer Huang, Fei Yang, Allison Creason, Christine Pak, Amiee Potter, Michael O Dorschner, Deborah A Nickerson, Peggy D Robertson,[...]. Am. J. Hum. Genet. 2018
11
18


Comparing ethnicity-based and expanded carrier screening methods at a single fertility center reveals significant differences in carrier rates and carrier couple rates.
Alexandra Peyser, Tomer Singer, Christine Mullin, Sara L Bristow, Amber Gamma, Kenan Onel, Avner Hershlag. Genet. Med. 2019
6
33

Advantages of expanded universal carrier screening: what is at stake?
Sanne van der Hout, Kim Ca Holtkamp, Lidewij Henneman, Guido de Wert, Wybo J Dondorp. Eur J Hum Genet 2016
18
16

Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology.
Julio Martin, Asan, Yuting Yi, Trinidad Alberola, Beatriz Rodríguez-Iglesias, Jorge Jiménez-Almazán, Qin Li, Huiqian Du, Pilar Alama, Amparo Ruiz,[...]. Fertil. Steril. 2015
29
16

Ethnicity-Based Carrier Screening.
Jennifer R King, Susan Klugman. Obstet. Gynecol. Clin. North Am. 2018
4
50


Expanded carrier screening in an infertile population: how often is clinical decision making affected?
Jason M Franasiak, Meir Olcha, Paul A Bergh, Kathleen H Hong, Marie D Werner, Eric J Forman, Rebekah S Zimmerman, Richard T Scott. Genet. Med. 2016
13
16


Screening for Tay-Sachs disease carriers by full-exon sequencing with novel variant interpretation outperforms enzyme testing in a pan-ethnic cohort.
Alana C Cecchi, Elizabeth S Vengoechea, Kristjan E Kaseniit, Melanie W Hardy, Laura A Kiger, Nikita Mehta, Imran S Haque, Krista Moyer, Patricia Z Page, Dale Muzzey,[...]. Mol Genet Genomic Med 2019
3
66

NGS-Based Assay for the Identification of Individuals Carrying Recessive Genetic Mutations in Reproductive Medicine.
Anna Abulí, Montserrat Boada, Benjamín Rodríguez-Santiago, Buenaventura Coroleu, Anna Veiga, Lluís Armengol, Pedro N Barri, Luis A Pérez-Jurado, Xavier Estivill. Hum. Mutat. 2016
22
16

Expanded carrier screening: A current perspective.
Enrica Mastantuoni, Gabriele Saccone, Huda B Al-Kouatly, Mariano Paternoster, Pietro D'Alessandro, Bruno Arduino, Luigi Carbone, Giuseppina Esposito, Antonio Raffone, Valentino De Vivo,[...]. Eur. J. Obstet. Gynecol. Reprod. Biol. 2018
7
28

A universal carrier test for the long tail of Mendelian disease.
Balaji S Srinivasan, Eric A Evans, Jason Flannick, A Scott Patterson, Christopher C Chang, Tuan Pham, Sharon Young, Amit Kaushal, James Lee, Jessica L Jacobson,[...]. Reprod. Biomed. Online 2010
58
16


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.