A citation-based method for searching scientific literature

Tiffany Wotton, Veronica Wiley, Bruce Bennetts, Louise Christie, Bridget Wilcken, Gemma Jenkins, Carolyn Rogers, Jackie Boyle, Michael Field. Int J Neonatal Screen 2018
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.
Donald B Bailey, Debra Skinner, Arlene M Davis, Ian Whitmarsh, Cynthia Powell. Pediatrics 2008
75
66

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
111
66

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.
Bradford Coffee, Krayton Keith, Igor Albizua, Tamika Malone, Julie Mowrey, Stephanie L Sherman, Stephen T Warren. Am J Hum Genet 2009
254
66

A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.
Stela Filipovic-Sadic, Sachin Sah, Liangjing Chen, Julie Krosting, Edward Sekinger, Wenting Zhang, Paul J Hagerman, Timothy T Stenzel, Andrew G Hadd, Gary J Latham,[...]. Clin Chem 2010
187
66

An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysis.
Liangjing Chen, Andrew Hadd, Sachin Sah, Stela Filipovic-Sadic, Julie Krosting, Edward Sekinger, Ruiqin Pan, Paul J Hagerman, Timothy T Stenzel, Flora Tassone,[...]. J Mol Diagn 2010
133
66

FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States.
Flora Tassone, Ka Pou Iong, Tzu-Han Tong, Joyce Lo, Louise W Gane, Elizabeth Berry-Kravis, Danh Nguyen, Lisa Y Mu, Jennifer Laffin, Don B Bailey,[...]. Genome Med 2012
188
33

Methylation analysis in newborn screening for fragile X syndrome.
David E Godler, David J Amor, Howard R Slater. JAMA Neurol 2014
4
33

Development and evaluation of quality control dried blood spot materials in newborn screening for lysosomal storage disorders.
Victor R De Jesus, X Kate Zhang, Joan Keutzer, Olaf A Bodamer, Adolf Mühl, Joseph J Orsini, Michele Caggana, Robert F Vogt, W Harry Hannon. Clin Chem 2009
104
33

Fragile X syndrome detection in newborns-pilot study.
Robert A Saul, Michael Friez, Karissa Eaves, Gail A Stapleton, Julianne S Collins, Charles E Schwartz, Roger E Stevenson. Genet Med 2008
28
33

Fragile X screening by quantification of FMRP in dried blood spots by a Luminex immunoassay.
Giuseppe LaFauci, Tatyana Adayev, Richard Kascsak, Regina Kascsak, Sarah Nolin, Pankaj Mehta, W Ted Brown, Carl Dobkin. J Mol Diagn 2013
38
33


Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.
Mei W Baker, Anne E Atkins, Suzanne K Cordovado, Miyono Hendrix, Marie C Earley, Philip M Farrell. Genet Med 2016
51
33

Fragile X Syndrome: Scientific Background and Screening Technologies.
Justine I Lyons, Gregory R Kerr, Patricia W Mueller. J Mol Diagn 2015
8
33

Fragile X syndrome: a review of clinical and molecular diagnoses.
Claudia Ciaccio, Laura Fontana, Donatella Milani, Silvia Tabano, Monica Miozzo, Susanna Esposito. Ital J Pediatr 2017
62
33


Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder.
Xiaoli Chen, Jingmin Wang, Hua Xie, Wenjuan Zhou, Ye Wu, Jun Wang, Jian Qin, Jin Guo, Qiang Gu, Xiaozhen Zhang,[...]. BMC Pediatr 2015
6
33

Current research, diagnosis, and treatment of fragile X-associated tremor/ataxia syndrome.
Zukhrofi Muzar, Reymundo Lozano. Intractable Rare Dis Res 2014
12
33

Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.
Ching-Cherng Tzeng, Li-Ping Tsai, Wuh-Liang Hwu, Shio-Jean Lin, Mei-Chyn Chao, Yuh-Jyh Jong, Shao-Yin Chu, Wei-Chen Chao, Chin-Li Lu. Am J Med Genet A 2005
45
33

Fragile X Newborn Screening: Lessons Learned From a Multisite Screening Study.
Donald B Bailey, Elizabeth Berry-Kravis, Louise W Gane, Sonia Guarda, Randi Hagerman, Cynthia M Powell, Flora Tassone, Anne Wheeler. Pediatrics 2017
18
33

Fragile X syndrome: a review of associated medical problems.
Sharon A Kidd, Ave Lachiewicz, Deborah Barbouth, Robin K Blitz, Carol Delahunty, Dianne McBrien, Jeannie Visootsak, Elizabeth Berry-Kravis. Pediatrics 2014
116
33

Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother-newborn pairs from the general population.
S Lévesque, C Dombrowski, M-L Morel, R Rehel, J-S Côté, J Bussières, K Morgan, F Rousseau. Clin Genet 2009
33
33

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation.
F Rousseau, D Heitz, V Biancalana, S Blumenfeld, C Kretz, J Boué, N Tommerup, C Van Der Hagen, C DeLozier-Blanchet, M F Croquette. N Engl J Med 1991
586
33

[Cutoff scores of the Ages and Stages Questionnaire-Chinese for screening infants and toddlers].
Guo-ying Yao, Xiao-yan Bian, Jane Squires, Mei Wei, Wei Song. Zhonghua Er Ke Za Zhi 2010
5
33

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
13
33

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
185
33

Emergence of Developmental Delay in Infants and Toddlers With an FMR1 Mutation.
Anne C Wheeler, Angela Gwaltney, Melissa Raspa, Katherine C Okoniewski, Elizabeth Berry-Kravis, Kelly N Botteron, Dejan Budimirovic, Heather Cody Hazlett, David Hessl, Molly Losh,[...]. Pediatrics 2021
2
50

Assessing the Fragile X Syndrome Newborn Screening Landscape.
Catharine Riley, Anne Wheeler. Pediatrics 2017
15
33

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission.
Carolyn M Yrigollen, Loreto Martorell, Blythe Durbin-Johnson, Montserrat Naudo, Jordi Genoves, Alessandra Murgia, Roberta Polli, Lili Zhou, Deborah Barbouth, Abigail Rupchock,[...]. J Neurodev Disord 2014
63
33


Autism Spectrum Disorder in Fragile X Syndrome: Cooccurring Conditions and Current Treatment.
Walter E Kaufmann, Sharon A Kidd, Howard F Andrews, Dejan B Budimirovic, Amy Esler, Barbara Haas-Givler, Tracy Stackhouse, Catharine Riley, Georgina Peacock, Stephanie L Sherman,[...]. Pediatrics 2017
102
33

Fragile X carrier screening and FMR1 allele distribution in the Japanese population.
Susumu Otsuka, Yumiko Sakamoto, Haruhiko Siomi, Mituo Itakura, Kenji Yamamoto, Hideo Matumoto, Tsukasa Sasaki, Nobumasa Kato, Eiji Nanba. Brain Dev 2010
40
33

Fragile X syndrome.
Randi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, Donald B Bailey, Herve Moine, R Frank Kooy, Flora Tassone, Ilse Gantois, Nahum Sonenberg, Jean Louis Mandel,[...]. Nat Rev Dis Primers 2017
239
33

Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population.
Wen Huang, Qiuping Xia, Shiyu Luo, Hua He, Ting Zhu, Qian Du, Ranhui Duan. Mol Genet Genomic Med 2015
9
33


Prolonged Time Lag to Final Diagnosis of Fragile X Syndrome.
Lidia V Gabis, Oded Hochberg, Odelia Leon Attia, Yonit Banet-Levi, Dana Topf, Shahar Shefer. J Pediatr 2018
8
33

Next-Generation Sequencing in Newborn Screening: A Review of Current State.
Ziga I Remec, Katarina Trebusak Podkrajsek, Barbka Repic Lampret, Jernej Kovac, Urh Groselj, Tine Tesovnik, Tadej Battelino, Marusa Debeljak. Front Genet 2021
11
33

Twenty-year follow-up of newborn screening for patients with muscular dystrophy.
Jeffrey Chung, Andrea L Smith, Sarah C Hughes, Gabriela Niizawa, Hoda Z Abdel-Hamid, Edwin W Naylor, Timothy Hughes, Paula R Clemens. Muscle Nerve 2016
18
33

Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.
Lainie Friedman Ross, Ellen Wright Clayton. Pediatrics 2019
19
33

Newborn screening for fragile X syndrome.
Flora Tassone. JAMA Neurol 2014
28
33

Therapeutic developments for Duchenne muscular dystrophy.
Ingrid E C Verhaart, Annemieke Aartsma-Rus. Nat Rev Neurol 2019
162
33

A vision of the future of newborn screening.
Duane Alexander, Peter C van Dyck. Pediatrics 2006
62
33

Changing perspectives on the benefits of newborn screening.
Donald B Bailey, Laura M Beskow, Arlene M Davis, Debra Skinner. Ment Retard Dev Disabil Res Rev 2006
35
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
23
33

Evidence-based care in Duchenne muscular dystrophy.
Craig M McDonald, Eugenio Mercuri. Lancet Neurol 2018
10
33



Corticosteroids for the treatment of Duchenne muscular dystrophy.
Emma Matthews, Ruth Brassington, Thierry Kuntzer, Fatima Jichi, Adnan Y Manzur. Cochrane Database Syst Rev 2016
190
33

The psychological impact of genetic information on children: a systematic review.
Claire E Wakefield, Lucy V Hanlon, Katherine M Tucker, Andrea F Patenaude, Christina Signorelli, Jordana K McLoone, Richard J Cohn. Genet Med 2016
59
33


Progress in treatment and newborn screening for Duchenne muscular dystrophy and spinal muscular atrophy.
Qing Ke, Zheng-Yan Zhao, Jerry R Mendell, Mei Baker, Veronica Wiley, Jennifer M Kwon, Lindsay N Alfano, Anne M Connolly, Catherine Jay, Hanna Polari,[...]. World J Pediatr 2019
8
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.