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R35 GM133747

Funded outputs count: 39
Funder award ID: R35 GM133747
OpenAlex ID: G469708262
Approximate Bayesian computation supports a high incidence of chromosomal mosaicism in blastocyst-stage human embryos
2025 · Qingya Yang, Sara A Carioscia, et al. · Genetics · 3
Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair
2025 · Jennifer H. McDaniel, Vaidehi Patel, et al. · Scientific Data · 12
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Chromosomal instability in human trophoblast stem cells and placentas
2025 · Danyang Wang, Andrew Cearlock, et al. · Nature Communications · 18
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Complete sequencing of ape genomes
2025 · DongAhn Yoo, Arang Rhie, et al. · Nature · 150
Common variation in meiosis genes shapes human recombination phenotypes and aneuploidy risk
2025 · Sara A. Carioscia, Arjun Biddanda, et al. · medRxiv · 2
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A T2T-CHM13 recombination map and globally diverse haplotype reference panel improves phasing and imputation
2025 · Joseph L. Lalli, Andrew N. Bortvin, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 6
The long and short of hyperdivergent regions
2024 · Nicolas D. Moya, Stephanie M. Yan, et al. · Trends in Genetics · 10
Sources of gene expression variation in a globally diverse human cohort
2024 · Dylan J. Taylor, Surya B. Chhetri, et al. · Nature · 79
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Interspecies regulatory landscapes and elements revealed by novel joint systematic integration of human and mouse blood cell epigenomes
2024 · Guanjue Xiang, Xi He, et al. · Genome Research · 7
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The complete sequence and comparative analysis of ape sex chromosomes
2024 · Kateryna D. Makova, Brandon D. Pickett, et al. · Nature · 120
Beyond the Human Genome Project: The Age of Complete Human Genome Sequences and Pangenome References
2024 · Dylan J. Taylor, Jordan M. Eizenga, et al. · Annual Review of Genomics and Human Genetics · 45
A rare genetic variant biases maternal meiotic recombination toward risk of pregnancy loss
2024 · Sara A. Carioscia, Rajiv C. McCoy · Nature Structural & Molecular Biology
Retinoic acid signaling regulates spatiotemporal specification of human green and red cones
2024 · Sarah E. Hadyniak, Joanna F. D. Hagen, et al. · PLoS Biology · 22
Aberrant landscapes of maternal meiotic crossovers contribute to aneuploidies in human embryos
2023 · Daniel Ariad, Svetlana Madjunkova, et al. · Genome Research · 12
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Identifying risk variants for embryo aneuploidy using ultra-low coverage whole-genome sequencing from preimplantation genetic testing
2023 · Siqi Sun, Mansour Aboelenain, et al. · The American Journal of Human Genetics · 17
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Meiotic and mitotic aneuploidies drive arrest of in vitro fertilized human preimplantation embryos
2023 · Rajiv C. McCoy, Michael C. Summers, et al. · Genome Medicine · 75
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The complete sequence of a human Y chromosome
2023 · Arang Rhie, Sergey Nurk, et al. · Nature · 468
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Identifying risk genes for embryo aneuploidy using ultra-low coverage whole-genome sequencing
2023 · Siqi Sun, Mansour Aboelenain, et al. · medRxiv
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Human embryo implantation
2023 · Joanne Muter, Vincent J. Lynch, et al. · Development · 125
Familial Clonal Hematopoiesis in a Long Telomere Syndrome
2023 · Emily A. DeBoy, Michael G. Tassia, et al. · New England Journal of Medicine · 146
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A method for low-coverage single-gamete sequence analysis demonstrates adherence to Mendel’s first law across a large sample of human sperm
2022 · Sara A Carioscia, Kathryn J Weaver, et al. · eLife · 11
The human embryonic genome is karyotypically complex, with chromosomally abnormal cells preferentially located away from the developing fetus
2022 · D K Griffin, P R Brezina, et al. · Human Reproduction · 42
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Meiotic and mitotic aneuploidies drive arrest of in vitro fertilized human preimplantation embryos
2022 · Rajiv C. McCoy, Michael C. Summers, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 2
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The complete sequence of a human genome
2022 · Sergey Nurk, Sergey Koren, et al. · Science · 3,063
A complete reference genome improves analysis of human genetic variation
2022 · Sergey Aganezov, Stephanie M. Yan, et al. · Science · 429
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