A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
110
46


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
81
43


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
163
29

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
426
27

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
26

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
123
23

Expanded carrier screening for monogenic disorders: where are we now?
Davit Chokoshvili, Danya Vears, Pascal Borry. Prenat Diagn 2018
39
56

Changing trends in carrier screening for genetic disease in the United States.
Shivani B Nazareth, Gabriel A Lazarin, James D Goldberg. Prenat Diagn 2015
40
47

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
48
37

Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases.
Mirjam Plantinga, Erwin Birnie, Kristin M Abbott, Richard J Sinke, Anneke M Lucassen, Juliette Schuurmans, Seyma Kaplan, Marian A Verkerk, Adelita V Ranchor, Irene M van Langen. Eur J Hum Genet 2016
40
42

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
25
68


Expanded carrier screening: A review of early implementation and literature.
Gabriel A Lazarin, Imran S Haque. Semin Perinatol 2016
36
44

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
28
57

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
23
69

The evolving landscape of expanded carrier screening: challenges and opportunities.
Stephanie A Kraft, Devan Duenas, Benjamin S Wilfond, Katrina A B Goddard. Genet Med 2019
26
61


Experiences among Women with Positive Prenatal Expanded Carrier Screening Results.
Erin Rothwell, Erin Johnson, Amber Mathiesen, Kylie Golden, Audrey Metcalf, Nancy C Rose, Jeffrey R Botkin. J Genet Couns 2017
26
53

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
23
60

Carrier screening in individuals of Ashkenazi Jewish descent.
Susan J Gross, Beth A Pletcher, Kristin G Monaghan. Genet Med 2008
120
13

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
268
13

Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples.
Caroline E Ghiossi, James D Goldberg, Imran S Haque, Gabriel A Lazarin, Kenny K Wong. J Genet Couns 2018
27
48

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
286
13

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
24
54


Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing.
Peter Benn, Audrey R Chapman, Kristine Erickson, Mark S Defrancesco, Louise Wilkins-Haug, James F X Egan, Jay Schulkin. Prenat Diagn 2014
50
24

Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. J Community Genet 2014
28
42

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
20
60

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
24
50

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
42
28

Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen.
Kyle A Beauchamp, Katherine A Johansen Taber, Dale Muzzey. Genet Med 2019
19
63


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
64
17



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
36
30

Genetic Counselors' Perspectives and Practices Regarding Expanded Carrier Screening after Initial Clinical Availability.
Gabriel A Lazarin, Stacey Detweiler, Shivani B Nazareth, Elena Ashkinadze. J Genet Couns 2016
17
58

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
38
26

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
15
66

Carrier screening by next-generation sequencing: health benefits and cost effectiveness.
Mohammad Azimi, Kyle Schmaus, Valerie Greger, Dana Neitzel, Robert Rochelle, Tuan Dinh. Mol Genet Genomic Med 2016
21
42

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
9

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers.
Pascal Borry, Lidewij Henneman, Phillis Lakeman, Leo P ten Kate, Martina C Cornel, Heidi C Howard. Hum Reprod 2011
57
15

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
11
81

ESHRE Task Force on Ethics and Law 21: genetic screening of gamete donors: ethical issues.
W Dondorp, G De Wert, G Pennings, F Shenfield, P Devroey, B Tarlatzis, P Barri, K Diedrich, U Eichenlaub-Ritter, F Tüttelmann,[...]. Hum Reprod 2014
27
33

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
28
32

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
761
9

Pregnant Women's Perspectives on Expanded Carrier Screening.
Lauren Propst, Gwendolyn Connor, Megan Hinton, Tabitha Poorvu, Jeffrey Dungan. J Genet Couns 2018
10
90

On the future of genetic risk assessment.
Hans-Hilger Ropers. J Community Genet 2012
39
20


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.