A citation-based method for searching scientific literature

Sarah T South, Charles Lee, Allen N Lamb, Anne W Higgins, Hutton M Kearney. Genet Med 2013
Times Cited: 161

List of shared articles

Times cited

European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019

Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Karen S Ho, Hope Twede, Rena Vanzo, Erin Harward, Charles H Hensel, Megan M Martin, Stephanie Page, Andreas Peiffer, Patricia Mowery-Rushton, Moises Serrano,[...]. Biomed Res Int 2016

Evaluation of the Affymetrix CytoScan(®) Dx Assay for developmental delay.
Bryn D Webb, Rebecca J Scharf, Emily A Spear, Lisa J Edelmann, Annemarie Stroustrup. Expert Rev Mol Diagn 2015

Limited diagnostic impact of duplications <1 Mb of uncertain clinical significance: a 10-year retrospective analysis of reporting practices at the Mayo Clinic.
Cherisse A Marcou, Beth Pitel, Clinton E Hagen, Nicole J Boczek, Ross A Rowsey, Linda B Baughn, Nicole L Hoppman, Erik C Thorland, Hutton M Kearney. Genet Med 2020

Clinical utility of array comparative genomic hybridisation in prenatal setting.
Luca Lovrecic, Ziga Iztok Remec, Marija Volk, Gorazd Rudolf, Karin Writzl, Borut Peterlin. BMC Med Genet 2016

Familial inheritance of the 3q29 microdeletion syndrome: case report and review.
Wahab A Khan, Ninette Cohen, Stuart A Scott, Elaine M Pereira. BMC Med Genomics 2019

Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing.
Fen-Xia Li, Mei-Juan Xie, Shou-Fang Qu, Dan He, Long Wu, Zhi-Kun Liang, Ying-Song Wu, Fang Yang, Xue-Xi Yang. Mol Med Rep 2020

Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Karen S Ho, E Robert Wassman, Adrianne L Baxter, Charles H Hensel, Megan M Martin, Aparna Prasad, Hope Twede, Rena J Vanzo, Merlin G Butler. Int J Mol Sci 2016

Chromosomal Microarray Detection of Constitutional Copy Number Variation Using Saliva DNA.
Jennifer Reiner, Lisa Karger, Ninette Cohen, Lakshmi Mehta, Lisa Edelmann, Stuart A Scott. J Mol Diagn 2017

Copy number variants, aneuploidies, and human disease.
Christa Lese Martin, Brianne E Kirkpatrick, David H Ledbetter. Clin Perinatol 2015

Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions.
Charles Hensel, Rena Vanzo, Megan Martin, Sean Dixon, Christophe Lambert, Brynn Levy, Lesa Nelson, Andy Peiffer, Karen S Ho, Patricia Rushton,[...]. PLoS Curr 2017

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders.
E Robert Wassman, Karen S Ho, Diana Bertrand, Kyle W Davis, Megan M Martin, Stephanie Page, Andreas Peiffer, Aparna Prasad, Moises A Serrano, Hope Twede,[...]. Neurol Genet 2019

SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
Guylaine D'Amours, Mathieu Langlois, Géraldine Mathonnet, Raouf Fetni, Sonia Nizard, Myriam Srour, Frédérique Tihy, Michael S Phillips, Jacques L Michaud, Emmanuelle Lemyre. BMC Med Genomics 2014

Describing sequencing results of structural chromosome rearrangements with a suggested next-generation cytogenetic nomenclature.
Zehra Ordulu, Kristen E Wong, Benjamin B Currall, Andrew R Ivanov, Shahrin Pereira, Sara Althari, James F Gusella, Michael E Talkowski, Cynthia C Morton. Am J Hum Genet 2014

Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome Sequence.
Christa Lese Martin, Dorothy Warburton. Annu Rev Genomics Hum Genet 2015

Use of Affymetrix Arrays in the Diagnosis of Gene Copy-Number Variation.
Farah R Zahir, Marco A Marra. Curr Protoc Hum Genet 2015

Copy number variants analysis in a cohort of isolated and syndromic developmental delay/intellectual disability reveals novel genomic disorders, position effects and candidate disease genes.
E Di Gregorio, E Riberi, E F Belligni, E Biamino, M Spielmann, U Ala, A Calcia, I Bagnasco, D Carli, G Gai,[...]. Clin Genet 2017