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Pille Hallast
Pille Hallast
The Jackson Laboratory for Genomic Medicine, CT, USA
在 jax.org 的电子邮件经过验证
标题
引用次数
年份
The complete sequence and comparative analysis of ape sex chromosomes
KD Makova, BD Pickett, RS Harris, GA Hartley, M Cechova, K Pal, S Nurk, ...
Nature, 1-11, 2024
132024
Structural polymorphism and diversity of human segmental duplications
H Jeong, PC Dishuck, DA Yoo, WT Harvey, KM Munson, AP Lewis, ...
bioRxiv, 2024.06. 04.597452, 2024
2024
Assembly of 43 human Y chromosomes reveals extensive complexity and variation
P Hallast, P Ebert, M Loftus, F Yilmaz, PA Audano, GA Logsdon, ...
Nature 621 (7978), 355-364, 2023
282023
High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing
F Yilmaz, U Gurusamy, TJ Mosley, P Hallast, K Kim, Y Mostovoy, ...
Genome medicine 15 (1), 35, 2023
42023
Optimized whole-genome CRISPR interference screens identify ARID1A-dependent growth regulators in human induced pluripotent stem cells
S Usluer, P Hallast, L Crepaldi, Y Zhou, K Urgo, C Dincer, J Su, G Noell, ...
Stem Cell Reports 18 (5), 1061-1074, 2023
52023
Assembly of 43 diverse human Y chromosomes reveals extensive complexity and variation
P Hallast, P Ebert, M Loftus, F Yilmaz, PA Audano, GA Logsdon, ...
bioRxiv, 2022.12. 01.518658, 2022
52022
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders
D Porubsky, W Höps, H Ashraf, PH Hsieh, B Rodriguez-Martin, F Yilmaz, ...
Cell 185 (11), 1986-2005. e26, 2022
802022
Placing ancient DNA sequences into reference phylogenies
R Martiniano, B De Sanctis, P Hallast, R Durbin
Molecular biology and evolution 39 (2), msac017, 2022
332022
Haplotype-resolved inversion landscape reveals hotspots of mutational recurrence associated with genomic disorders
D Porubsky, W Höps, H Ashraf, PH Hsieh, B Rodriguez-Martin, F Yilmaz, ...
bioRxiv, 2021.12. 20.472354, 2021
92021
The genomic history of the Middle East
MA Almarri, M Haber, RA Lootah, P Hallast, S Al Turki, HC Martin, Y Xue, ...
Cell 184 (18), 4612-4625. e14, 2021
352021
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans
P Hallast, L Kibena, M Punab, E Arciero, S Rootsi, M Grigorova, R Flores, ...
Elife 10, e65420, 2021
172021
Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain
GM Lall, MHD Larmuseau, JH Wetton, C Batini, P Hallast, TI Huszar, ...
European Journal of Human Genetics 29 (3), 512-523, 2021
112021
A Southeast Asian origin for present-day non-African human Y chromosomes
P Hallast, A Agdzhoyan, O Balanovsky, Y Xue, C Tyler-Smith
Human genetics 140, 299-307, 2021
252021
Insights into human genetic variation and population history from 929 diverse genomes
A Bergström, SA McCarthy, R Hui, MA Almarri, Q Ayub, P Danecek, ...
Science 367 (6484), eaay5012, 2020
6252020
Population-genetic and functional investigation of high altitude adaptation in the Himalayan populations
E Arciero, M Haber, T Kraaijenbrink, Asan, M Szpak, P Hallast, ...
AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 171, 9-9, 2020
2020
Insights into human genetic variation and population history from 929 diverse genomes. Science
A Bergstrom, SA McCarthy, R Hui, MA Almarri, Q Ayub, P Danecek, ...
32020
Early replacement of West Eurasian male Y chromosomes from the east
P Hallast, A Agdzhoyan, O Balanovsky, Y Xue, C Tyler-Smith
bioRxiv, 867317, 2019
42019
Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome
W Shi, A Massaia, S Louzada, J Handsaker, W Chow, S McCarthy, ...
Genome biology 20, 1-12, 2019
112019
Massively parallel sequencing of autosomal STRs and identity-informative SNPs highlights consanguinity in Saudi Arabia
YM Khubrani, P Hallast, MA Jobling, JH Wetton
Forensic Science International: Genetics 43, 102164, 2019
332019
Human Y chromosome exerts pleiotropic effects on susceptibility to atherosclerosis
JM Eales, AA Maan, X Xu, T Michoel, P Hallast, C Batini, D Zadik, ...
Arteriosclerosis, thrombosis, and vascular biology 39 (11), 2386-2401, 2019
442019
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