Eric Evans
Eric Evans
CSO, Natera
Verified email at
Cited by
Cited by
An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals
GA Lazarin, IS Haque, S Nazareth, K Iori, AS Patterson, JL Jacobson, ...
Genetics in Medicine 15 (3), 178-186, 2013
Pseudomonas aeruginosa Suppresses Host Immunity by Activating the DAF-2 Insulin-Like Signaling Pathway in Caenorhabditis elegans
EA Evans, T Kawli, MW Tan
PLoS pathogens 4 (10), e1000175, 2008
Modeled fetal risk of genetic diseases identified by expanded carrier screening
IS Haque, GA Lazarin, HP Kang, EA Evans, JD Goldberg, RJ Wapner
Jama 316 (7), 734-742, 2016
Understanding the basics of NGS: from mechanism to variant calling
D Muzzey, EA Evans, C Lieber
Current genetic medicine reports 3 (4), 158-165, 2015
The DAF‐2 insulin‐like signaling pathway independently regulates aging and immunity in C. elegans
EA Evans, WC Chen, MW Tan
Aging cell 7 (6), 879-893, 2008
Systematic classification of disease severity for evaluation of expanded carrier screening panels
GA Lazarin, F Hawthorne, NS Collins, EA Platt, EA Evans, IS Haque
PLoS One 9 (12), e114391, 2014
A universal carrier test for the long tail of Mendelian disease
BS Srinivasan, EA Evans, J Flannick, AS Patterson, CC Chang, T Pham, ...
Reproductive biomedicine online 21 (4), 537-551, 2010
System and methods for detecting genetic variation
H Richards, E Evans, B Srinivasan, S Srinivasan, S Abhik, AS Patterson, ...
US Patent 9,092,401, 2015
Validation of an expanded carrier screen that optimizes sensitivity via full-exon sequencing and panel-wide copy number variant identification
GJ Hogan, VS Vysotskaia, KA Beauchamp, S Seisenberger, PV Grauman, ...
Clinical chemistry 64 (7), 1063-1073, 2018
Systematic design and comparison of expanded carrier screening panels
KA Beauchamp, D Muzzey, KK Wong, GJ Hogan, K Karimi, SI Candille, ...
Genetics in Medicine 20 (1), 55-63, 2018
SPAM1 (PH-20) protein and mRNA expression in the epididymides of humans and macaques: utilizing laser microdissection/RT-PCR
EA Evans, H Zhang, PA Martin-DeLeon
Reproductive Biology and Endocrinology 1, 1-12, 2003
Nucleic acid sequencing adapters and uses thereof
EA Evans, IS Haque, K Beauchamp, C Chu, CG Artieri, N Welker
US Patent 11,708,574, 2023
Combinatorial DNA screening
JR Maguire, C Chu, IS Haque, EA Evans, N Welker
US Patent 10,597,717, 2020
Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods
CG Artieri, C Haverty, EA Evans, JD Goldberg, IS Haque, Y Yaron, ...
Prenatal diagnosis 37 (5), 482-490, 2017
Smith–Lemli–Opitz syndrome carrier frequency and estimates of in utero mortality rates
GA Lazarin, IS Haque, EA Evans, JD Goldberg
Prenatal Diagnosis 37 (4), 350-355, 2017
Methods of predicting pathogenicity of genetic sequence variants
IS Haque, EA Evans, SM Vikram, MD Rasmussen
US Patent App. 15/189,957, 2016
Methods and compositions for high-throughput sequencing
H Richards, E Evans, B Srinivasan, S Srinivasan, C Chu
US Patent App. 13/551,587, 2014
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment
VS Vysotskaia, GJ Hogan, GM Gould, X Wang, AD Robertson, KR Haas, ...
PeerJ 5, e3046, 2017
Systems and methods for prenatal genetic analysis
E Evans, C Chu, D Davison, H Richards
US Patent App. 14/207,141, 2014
Methods and compositions for enrichment of target polynucleotides
H Richards, E Evans, B Srinivasan, S Srinivasan, C Chu
US Patent App. 13/551,590, 2014
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