A citation-based method for searching scientific literature

Katherine Johansen Taber, Jeraldine Lim-Harashima, Harris Naemi, Jim Goldberg. Mol Genet Genomic Med 2019
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity



Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles.
Sarah L Nolin, Anne Glicksman, Nicole Tortora, Emily Allen, James Macpherson, Montserrat Mila, Angela M Vianna-Morgante, Stephanie L Sherman, Carl Dobkin, Gary J Latham,[...]. Am J Med Genet A 2019
17
60

"It's about having the choice": stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome.
Alison D Archibald, Chriselle L Hickerton, Alice M Jaques, Samantha Wake, Jonathan Cohen, Sylvia A Metcalfe. Am J Med Genet A 2013
21
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
44
60

Preconceptional and prenatal screening for fragile X syndrome: experience with 40,000 tests.
Michal Berkenstadt, Liat Ries-Levavi, Howard Cuckle, Leah Peleg, Gad Barkai. Prenat Diagn 2007
64
60

Epidemiology of fragile X syndrome: a systematic review and meta-analysis.
Jessica Hunter, Oliver Rivero-Arias, Angel Angelov, Edward Kim, Iain Fotheringham, Jose Leal. Am J Med Genet A 2014
143
60

Fragile X syndrome carrier screening in pregnant women in Chinese Han population.
Chia-Cheng Hung, Chien-Nan Lee, Yu-Chu Wang, Chih-Ling Chen, Tze-Kang Lin, Yi-Ning Su, Ming-Wei Lin, Jessica Kang, Yi-Yun Tai, Wen-Wei Hsu,[...]. Sci Rep 2019
6
60

Fragile X syndrome: diagnostic and carrier testing.
Stephanie Sherman, Beth A Pletcher, Deborah A Driscoll. Genet Med 2005
182
40

Attitudes toward prenatal screening and testing for Fragile X.
Joanna H Fanos, Kerstin A Spangner, Thomas J Musci. Genet Med 2006
33
40

Fragile X population carrier screening.
Sylvia A Metcalfe, Martin B Delatycki, Jonathan Cohen, Alison D Archibald, Jon D Emery. Genet Med 2018
4
50

AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.
Carolyn M Yrigollen, Blythe Durbin-Johnson, Louise Gane, David L Nelson, Randi Hagerman, Paul J Hagerman, Flora Tassone. Genet Med 2012
98
40


Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.
Sarah L Nolin, W Ted Brown, Anne Glicksman, George E Houck, Alice D Gargano, Amy Sullivan, Valérie Biancalana, Karen Bröndum-Nielsen, Helle Hjalgrim, Elke Holinski-Feder,[...]. Am J Hum Genet 2003
240
40


Caregiver opinions about fragile X population screening.
Donald B Bailey, Ellen Bishop, Melissa Raspa, Debra Skinner. Genet Med 2012
18
40

Early Identification of Fragile X Syndrome through Expanded Newborn Screening.
Katherine C Okoniewski, Anne C Wheeler, Stacey Lee, Beth Boyea, Melissa Raspa, Jennifer L Taylor, Donald B Bailey. Brain Sci 2019
7
40

Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population.
Sébastien Jacquemont, Randi J Hagerman, Maureen A Leehey, Deborah A Hall, Richard A Levine, James A Brunberg, Lin Zhang, Tristan Jardini, Louise W Gane, Susan W Harris,[...]. JAMA 2004
423
40

Informed decision making and psychosocial outcomes in pregnant and nonpregnant women offered population fragile X carrier screening.
Sylvia A Metcalfe, Melissa Martyn, Alice Ames, Vicki Anderson, Alison D Archibald, Grad Dip Gen Couns, Rob Carter, Jonathan Cohen, Megan Cotter, M GenCouns,[...]. Genet Med 2017
10
40

Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).
Heather S Hipp, Krista H Charen, Jessica B Spencer, Emily G Allen, Stephanie L Sherman. Menopause 2016
19
40

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
A J Verkerk, M Pieretti, J S Sutcliffe, Y H Fu, D P Kuhl, A Pizzuti, O Reiner, S Richards, M F Victoria, F P Zhang. Cell 1991
40


Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy.
Fei Gao, Wen Huang, Yanjun You, Jie Huang, Juan Zhao, Jin Xue, Huaixing Kang, Yingbao Zhu, Zhengmao Hu, Emily G Allen,[...]. Mol Genet Genomic Med 2020
3
66


Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience.
Simon Ardui, Valerie Race, Thomy de Ravel, Hilde Van Esch, Koenraad Devriendt, Gert Matthijs, Joris R Vermeesch. Front Genet 2018
10
20

Fragile X screening: attitudes of genetic health professionals.
Kruti Acharya, Lainie Friedman Ross. Am J Med Genet A 2009
24
20

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
29
20

Fragile X analysis of 1112 prenatal samples from 1991 to 2010.
Sarah L Nolin, Anne Glicksman, Xiaohua Ding, Nicole Ersalesi, W Ted Brown, Stephanie L Sherman, Carl Dobkin. Prenat Diagn 2011
68
20

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
20

Prenatal carrier testing for fragile X: counseling issues and challenges.
Thomas J Musci, Krista Moyer. Obstet Gynecol Clin North Am 2010
12
20

International perspectives on the implementation of reproductive carrier screening.
Martin B Delatycki, Fowzan Alkuraya, Alison Archibald, Carlo Castellani, Martina Cornel, Wayne W Grody, Lidewij Henneman, Adonis S Ioannides, Edwin Kirk, Nigel Laing,[...]. Prenat Diagn 2020
20
20

Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.
Brenda Finucane, Liane Abrams, Amy Cronister, Alison D Archibald, Robin L Bennett, Allyn McConkie-Rosell. J Genet Couns 2012
36
20

Technology-Driven Noninvasive Prenatal Screening Results Disclosure and Management.
Aishwarya Arjunan, Rotem Ben-Shachar, Jamie Kostialik, Katherine Johansen Taber, Gabriel A Lazarin, Elizabeth Denne, Dale Muzzey, Carrie Haverty. Telemed J E Health 2020
4
25

Discovering fragile X syndrome: family experiences and perceptions.
Donald B Bailey, Debra Skinner, Karen L Sparkman. Pediatrics 2003
73
20

Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.
Jeanna M McCuaig, Susan Randall Armel, Melanie Care, Alexandra Volenik, Raymond H Kim, Kelly A Metcalfe. Cancers (Basel) 2018
29
20


Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.
H Toledano-Alhadef, L Basel-Vanagaite, N Magal, B Davidov, S Ehrlich, V Drasinover, E Taub, G J Halpern, N Ginott, M Shohat. Am J Hum Genet 2001
139
20

Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
Amy Cronister, Jennifer Teicher, Elizabeth M Rohlfs, Alan Donnenfeld, Stephanie Hallam. Obstet Gynecol 2008
56
20

Projecting the Supply and Demand for Certified Genetic Counselors: a Workforce Study.
Jennifer M Hoskovec, R L Bennett, M E Carey, J E DaVanzo, M Dougherty, S E Hahn, B S LeRoy, S O'Neal, J G Richardson, C A Wicklund. J Genet Couns 2018
114
20

Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.
Marc D Schwartz, Heiddis B Valdimarsdottir, Beth N Peshkin, Jeanne Mandelblatt, Rachel Nusbaum, An-Tsun Huang, Yaojen Chang, Kristi Graves, Claudine Isaacs, Marie Wood,[...]. J Clin Oncol 2014
148
20



Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.
Barbara B Biesecker, Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Erin Turbitt, Kristen P Fishler, John H Patton, Ilana M Miller, Alexis R Heidlebaugh, Leslie G Biesecker. JAMA Intern Med 2018
42
20

FMR1 allele size distribution in 35,000 males and females: a comparison of developmental delay and general population cohorts.
Claudine M Kraan, Quang M Bui, Mike Field, Alison D Archibald, Sylvia A Metcalfe, Louise M Christie, Bruce H Bennetts, Ralph Oertel, Melanie J Smith, Desiree du Sart,[...]. Genet Med 2018
12
20

The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspective.
Gary J Latham, Justine Coppinger, Andrew G Hadd, Sarah L Nolin. Front Genet 2014
27
20

Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial.
Katie L Lewis, Kendall L Umstead, Jennifer J Johnston, Ilana M Miller, Lydia J Thompson, Kristen P Fishler, Leslie G Biesecker, Barbara B Biesecker. Am J Hum Genet 2018
10
20

Who should be tested for fragile X carriership? A review of 1 center's pedigrees.
Krishna Rajendra, Jay J Bringman, Jewel Ward, Owen P Phillips. Am J Obstet Gynecol 2008
4
25

Screening for fragile X syndrome in women of reproductive age.
R Pesso, M Berkenstadt, H Cuckle, E Gak, L Peleg, M Frydman, G Barkai. Prenat Diagn 2000
83
20

Who self-identifies as disabled? An examination of impairment and contextual predictors.
Kathleen R Bogart, Adena Rottenstein, Emily M Lund, Lauren Bouchard. Rehabil Psychol 2017
3
33

Attitudes of mothers of children with down syndrome towards noninvasive prenatal testing.
Gregory Kellogg, Leah Slattery, Louanne Hudgins, Kelly Ormond. J Genet Couns 2014
45
20

No change in the age of diagnosis for fragile x syndrome: findings from a national parent survey.
Donald B Bailey, Melissa Raspa, Ellen Bishop, David Holiday. Pediatrics 2009
103
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.