A citation-based method for searching scientific literature

Lidewij Henneman, Pascal Borry, Davit Chokoshvili, Martina C Cornel, Carla G van El, Francesca Forzano, Alison Hall, Heidi C Howard, Sandra Janssens, Hülya Kayserili, Phillis Lakeman, Anneke Lucassen, Sylvia A Metcalfe, Lovro Vidmar, Guido de Wert, Wybo J Dondorp, Borut Peterlin. Eur J Hum Genet 2016
Times Cited: 121







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



Times Cited
  Times     Co-cited
Similarity




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
431
27

Expanded carrier screening for monogenic disorders: where are we now?
Davit Chokoshvili, Danya Vears, Pascal Borry. Prenat Diagn 2018
40
67

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
42
61

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
171
24

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
87
26


Preconception care and genetic risk: ethical issues.
Guido M W R De Wert, Wybo J Dondorp, Bartha M Knoppers. J Community Genet 2012
45
40

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
132
18

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
51
35

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
30
60

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
43
39

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
37

Expanded carrier screening: A review of early implementation and literature.
Gabriel A Lazarin, Imran S Haque. Semin Perinatol 2016
36
47

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
32
53

On the future of genetic risk assessment.
Hans-Hilger Ropers. J Community Genet 2012
41
39

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
15


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
25
56

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

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
46
28

Measuring the impact of genetic knowledge on intentions and attitudes of the community towards expanded preconception carrier screening.
Royston Ong, Denise Howting, Alethea Rea, Hayley Christian, Pauline Charman, Caron Molster, Gianina Ravenscroft, Nigel George Laing. J Med Genet 2018
19
68

Carrier screening in individuals of Ashkenazi Jewish descent.
Susan J Gross, Beth A Pletcher, Kristin G Monaghan. Genet Med 2008
123
12

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
18


Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives.
Kim C A Holtkamp, Inge B Mathijssen, Phillis Lakeman, Merel C van Maarle, Wybo J Dondorp, Lidewij Henneman, Martina C Cornel. Eur J Public Health 2017
22
54

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
26
46



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
53
20

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
58
18

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
26
42

Swedish parents' interest in preconception genetic carrier screening.
Maria Ekstrand Ragnar, Tanja Tydén, Ulrik Kihlbom, Margareta Larsson. Ups J Med Sci 2016
17
64

Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen.
Kyle A Beauchamp, Katherine A Johansen Taber, Dale Muzzey. Genet Med 2019
23
47

Evaluation of a multi-disease carrier screening programme in Ashkenazi Jewish high schools.
L Ioannou, J Massie, S Lewis, V Petrou, A Gason, S Metcalfe, M A Aitken, A Bankier, M B Delatycki. Clin Genet 2010
30
33


Feasibility of couple-based expanded carrier screening offered by general practitioners.
Juliette Schuurmans, Erwin Birnie, Lieke M van den Heuvel, Mirjam Plantinga, Anneke Lucassen, Dorina M van der Kolk, Kristin M Abbott, Adelita V Ranchor, Agnes D Diemers, Irene M van Langen. Eur J Hum Genet 2019
16
62

Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?
Phillis Lakeman, Anne Marie Catharina Plass, Lidewij Henneman, Pieter Dirk Bezemer, Martina Cornelia Cornel, Leo Pieter ten Kate. Eur J Hum Genet 2009
34
26

"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
31
29

Carrier screening for beta-thalassaemia: a review of international practice.
Nicole E Cousens, Clara L Gaff, Sylvia A Metcalfe, Martin B Delatycki. Eur J Hum Genet 2010
99
9

'It is not in my world': an exploration of attitudes and influences associated with cystic fibrosis carrier screening.
Belinda J McClaren, Martin B Delatycki, Veronica Collins, Sylvia A Metcalfe, MaryAnne Aitken. Eur J Hum Genet 2008
45
20

Expanded carrier screening panels-does bigger mean better?
Sara Wienke, Kimberly Brown, Meagan Farmer, Charlie Strange. J Community Genet 2014
30
30


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
21
42

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
25

Expanded carrier screening for autosomal recessive conditions in health care: Arguments for a couple-based approach and examination of couples' views.
Mirjam Plantinga, Erwin Birnie, Juliette Schuurmans, Anne H Buitenhuis, Elise Boersma, Anneke M Lucassen, Marian A Verkerk, Irene M van Langen, Adelita V Ranchor. Prenat Diagn 2019
11
81

Attitudes of the general population towards preconception expanded carrier screening for autosomal recessive disorders including inborn errors of metabolism.
Stephanie C M Nijmeijer, Thirsa Conijn, Phillis Lakeman, Lidewij Henneman, Frits A Wijburg, Lotte Haverman. Mol Genet Metab 2019
15
60


Carrier screening for recessive disorders.
Stylianos E Antonarakis. Nat Rev Genet 2019
26
34


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.