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
31


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
12

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
4

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
0

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
9

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
5

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
1

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
25

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
8

Copy number variants, aneuploidies, and human disease.
Christa Lese Martin, Brianne E Kirkpatrick, David H Ledbetter. Clin Perinatol 2015
33

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
9

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
1

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
10

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
34

Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome Sequence.
Christa Lese Martin, Dorothy Warburton. Annu Rev Genomics Hum Genet 2015
23

Use of Affymetrix Arrays in the Diagnosis of Gene Copy-Number Variation.
Farah R Zahir, Marco A Marra. Curr Protoc Hum Genet 2015
9

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
22