Kendra Hoekzema
Kendra Hoekzema
Faculty Research Assistant, Oregon State University
Verified email at
Cited by
Cited by
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ...
Nature genetics 49 (4), 515-526, 2017
Discovery and genotyping of structural variation from long-read haploid genome sequence data
J Huddleston, MJP Chaisson, KM Steinberg, W Warren, K Hoekzema, ...
Genome research 27 (5), 677-685, 2017
High-resolution comparative analysis of great ape genomes
ZN Kronenberg, IT Fiddes, D Gordon, S Murali, S Cantsilieris, ...
Science 360 (6393), eaar6343, 2018
A draft human pangenome reference
WW Liao, M Asri, J Ebler, D Doerr, M Haukness, G Hickey, S Lu, JK Lucas, ...
Nature 617 (7960), 312-324, 2023
De novo genic mutations among a Chinese autism spectrum disorder cohort
T Wang, H Guo, B Xiong, HAF Stessman, H Wu, BP Coe, TN Turner, Y Liu, ...
Nature communications 7 (1), 13316, 2016
Genomic patterns of de novo mutation in simplex autism
TN Turner, BP Coe, DE Dickel, K Hoekzema, BJ Nelson, MC Zody, ...
Cell 171 (3), 710-722. e12, 2017
Genome sequencing of autism-affected families reveals disruption of putative noncoding regulatory DNA
TN Turner, F Hormozdiari, MH Duyzend, SA McClymont, PW Hook, ...
The American Journal of Human Genetics 98 (1), 58-74, 2016
The structure, function and evolution of a complete human chromosome 8
GA Logsdon, MR Vollger, PH Hsieh, Y Mao, MA Liskovykh, S Koren, ...
Nature 593 (7857), 101-107, 2021
Segmental duplications and their variation in a complete human genome
MR Vollger, X Guitart, PC Dishuck, L Mercuri, WT Harvey, A Gershman, ...
Science 376 (6588), eabj6965, 2022
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
MR Geisheker, G Heymann, T Wang, BP Coe, TN Turner, HAF Stessman, ...
Nature neuroscience 20 (8), 1043-1051, 2017
Disruption of POGZ is associated with intellectual disability and autism spectrum disorders
HAF Stessman, MH Willemsen, M Fenckova, O Penn, A Hoischen, ...
The American Journal of Human Genetics 98 (3), 541-552, 2016
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
T Wang, K Hoekzema, D Vecchio, H Wu, A Sulovari, BP Coe, ...
Nature communications 11 (1), 4932, 2020
The evolution and population diversity of human-specific segmental duplications
MY Dennis, L Harshman, BJ Nelson, O Penn, S Cantsilieris, J Huddleston, ...
Nature ecology & evolution 1 (3), 0069, 2017
Targeted long-read sequencing identifies missing disease-causing variation
DE Miller, A Sulovari, T Wang, H Loucks, K Hoekzema, KM Munson, ...
The American Journal of Human Genetics 108 (8), 1436-1449, 2021
denovo-db: a compendium of human de novo variants
TN Turner, Q Yi, N Krumm, J Huddleston, K Hoekzema, HA F. Stessman, ...
Nucleic acids research 45 (D1), D804-D811, 2017
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes
H Guo, MH Duyzend, BP Coe, C Baker, K Hoekzema, J Gerdts, TN Turner, ...
Genetics in Medicine 21 (7), 1611-1620, 2019
What influences the worldwide genetic structure of sperm whales (Physeter macrocephalus)?
A Alexander, D Steel, K Hoekzema, SL Mesnick, D Engelhaupt, I Kerr, ...
Molecular ecology 25 (12), 2754-2772, 2016
Recent ultra-rare inherited variants implicate new autism candidate risk genes
AB Wilfert, TN Turner, SC Murali, PH Hsieh, A Sulovari, T Wang, BP Coe, ...
Nature genetics 53 (8), 1125-1134, 2021
Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes
PH Hsieh, MR Vollger, V Dang, D Porubsky, C Baker, S Cantsilieris, ...
Science 366 (6463), eaax2083, 2019
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
MA Gillentine, T Wang, K Hoekzema, J Rosenfeld, P Liu, H Guo, CN Kim, ...
Genome medicine 13, 1-26, 2021
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