| Year |
Citation |
Score |
| 2023 |
Makova KD, Pickett BD, Harris RS, Hartley GA, Cechova M, Pal K, Nurk S, Yoo D, Li Q, Hebbar P, McGrath BC, Antonacci F, Aubel M, Biddanda A, Borchers M, ... ... Hallast P, et al. The Complete Sequence and Comparative Analysis of Ape Sex Chromosomes. Biorxiv : the Preprint Server For Biology. PMID 38077089 DOI: 10.1101/2023.11.30.569198 |
0.501 |
|
| 2023 |
Hallast P, Ebert P, Loftus M, Yilmaz F, Audano PA, Logsdon GA, Bonder MJ, Zhou W, Höps W, Kim K, Li C, Hoyt SJ, Dishuck PC, Porubsky D, Tsetsos F, et al. Assembly of 43 human Y chromosomes reveals extensive complexity and variation. Nature. PMID 37612510 DOI: 10.1038/s41586-023-06425-6 |
0.567 |
|
| 2023 |
Yilmaz F, Gurusamy U, Mosley TJ, Hallast P, Kim K, Mostovoy Y, Purcell RH, Shaikh TH, Zwick ME, Kwok PY, Lee C, Mulle JG. High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing. Genome Medicine. 15: 35. PMID 37165454 DOI: 10.1186/s13073-023-01184-5 |
0.497 |
|
| 2022 |
Porubsky D, Höps W, Ashraf H, Hsieh P, Rodriguez-Martin B, Yilmaz F, Ebler J, Hallast P, Maria Maggiolini FA, Harvey WT, Henning B, Audano PA, Gordon DS, Ebert P, Hasenfeld P, et al. Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders. Cell. PMID 35525246 DOI: 10.1016/j.cell.2022.04.017 |
0.5 |
|
| 2022 |
Martiniano R, De Sanctis B, Hallast P, Durbin R. Placing Ancient DNA Sequences into Reference Phylogenies. Molecular Biology and Evolution. 39. PMID 35084493 DOI: 10.1093/molbev/msac017 |
0.334 |
|
| 2021 |
Almarri MA, Haber M, Lootah RA, Hallast P, Al Turki S, Martin HC, Xue Y, Tyler-Smith C. The genomic history of the Middle East. Cell. PMID 34352227 DOI: 10.1016/j.cell.2021.07.013 |
0.371 |
|
| 2021 |
Hallast P, Kibena L, Punab M, Arciero E, Rootsi S, Grigorova M, Flores R, Jobling MA, Poolamets O, Pomm K, Korrovits P, Rull K, Xue Y, Tyler-Smith C, Laan M. A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans. Elife. 10. PMID 33781384 DOI: 10.7554/eLife.65420 |
0.45 |
|
| 2020 |
Lall GM, Larmuseau MHD, Wetton JH, Batini C, Hallast P, Huszar TI, Zadik D, Aase S, Baker T, Balaresque P, Bodmer W, Børglum AD, de Knijff P, Dunn H, Harding SE, et al. Subdividing Y-chromosome haplogroup R1a1 reveals Norse Viking dispersal lineages in Britain. European Journal of Human Genetics : Ejhg. PMID 33139852 DOI: 10.1038/s41431-020-00747-z |
0.349 |
|
| 2020 |
Hallast P, Agdzhoyan A, Balanovsky O, Xue Y, Tyler-Smith C. A Southeast Asian origin for present-day non-African human Y chromosomes. Human Genetics. PMID 32666166 DOI: 10.1007/S00439-020-02204-9 |
0.407 |
|
| 2020 |
Bergström A, McCarthy SA, Hui R, Almarri MA, Ayub Q, Danecek P, Chen Y, Felkel S, Hallast P, Kamm J, Blanché H, Deleuze JF, Cann H, Mallick S, Reich D, et al. Insights into human genetic variation and population history from 929 diverse genomes. Science (New York, N.Y.). 367. PMID 32193295 DOI: 10.1126/Science.Aay5012 |
0.375 |
|
| 2019 |
Eales JM, Maan AA, Xu X, Michoel T, Hallast P, Batini C, Zadik D, Prestes PR, Molina E, Denniff M, Schroeder J, Bjorkegren JLM, Thompson J, Maffia P, Guzik TJ, et al. Human Y Chromosome Exerts Pleiotropic Effects on Susceptibility to Atherosclerosis. Arteriosclerosis, Thrombosis, and Vascular Biology. 39: 2386-2401. PMID 31644355 DOI: 10.1161/ATVBAHA.119.312405 |
0.411 |
|
| 2019 |
Shi W, Massaia A, Louzada S, Handsaker J, Chow W, McCarthy S, Collins J, Hallast P, Howe K, Church DM, Yang F, Xue Y, Tyler-Smith C. Birth, expansion, and death of VCY-containing palindromes on the human Y chromosome. Genome Biology. 20: 207. PMID 31610793 DOI: 10.1186/S13059-019-1816-Y |
0.546 |
|
| 2019 |
Shi W, Louzada S, Grigorova M, Massaia A, Arciero E, Kibena L, Ge XJ, Chen Y, Ayub Q, Poolamets O, Tyler-Smith C, Punab M, Laan M, Yang F, Hallast P, et al. Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome. Human Molecular Genetics. PMID 31108506 DOI: 10.1093/Hmg/Ddz101 |
0.456 |
|
| 2017 |
Shi W, Massaia A, Louzada S, Banerjee R, Hallast P, Chen Y, Bergström A, Gu Y, Leonard S, Quail MA, Ayub Q, Yang F, Tyler-Smith C, Xue Y. Copy number variation arising from gene conversion on the human Y chromosome. Human Genetics. PMID 29209947 DOI: 10.1007/S00439-017-1857-9 |
0.58 |
|
| 2016 |
Haber M, Mezzavilla M, Bergström A, Prado-Martinez J, Hallast P, Saif-Ali R, Al-Habori M, Dedoussis G, Zeggini E, Blue-Smith J, Wells RS, Xue Y, Zalloua PA, Tyler-Smith C. Chad Genetic Diversity Reveals an African History Marked by Multiple Holocene Eurasian Migrations. American Journal of Human Genetics. PMID 27889059 DOI: 10.1016/J.Ajhg.2016.10.012 |
0.454 |
|
| 2016 |
de Manuel M, Kuhlwilm M, Frandsen P, Sousa VC, Desai T, Prado-Martinez J, Hernandez-Rodriguez J, Dupanloup I, Lao O, Hallast P, Schmidt JM, Heredia-Genestar JM, Benazzo A, Barbujani G, Peter BM, et al. Chimpanzee genomic diversity reveals ancient admixture with bonobos. Science (New York, N.Y.). 354: 477-481. PMID 27789843 DOI: 10.1126/Science.Aag2602 |
0.391 |
|
| 2016 |
Hallast P, Maisano Delser P, Batini C, Zadik D, Rocchi M, Schempp W, Tyler-Smith C, Jobling MA. Great ape Y Chromosome and mitochondrial DNA phylogenies reflect subspecies structure and patterns of mating and dispersal. Genome Research. 26: 427-39. PMID 26883546 DOI: 10.1101/Gr.198754.115 |
0.441 |
|
| 2015 |
Hallast P, Batini C, Zadik D, Maisano Delser P, Wetton JH, Arroyo-Pardo E, Cavalleri GL, de Knijff P, Destro Bisol G, Dupuy BM, Eriksen HA, Jorde LB, King TE, Larmuseau MH, López de Munain A, et al. The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades. Molecular Biology and Evolution. 32: 661-73. PMID 25468874 DOI: 10.1093/Molbev/Msu327 |
0.433 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2015 |
Batini C, Hallast P, Zadik D, Delser PM, Benazzo A, Ghirotto S, Arroyo-Pardo E, Cavalleri GL, de Knijff P, Dupuy BM, Eriksen HA, King TE, López de Munain A, López-Parra AM, Loutradis A, et al. Large-scale recent expansion of European patrilineages shown by population resequencing. Nature Communications. 6: 7152. PMID 25988751 DOI: 10.1038/ncomms8152 |
0.283 |
|
| 2023 |
Usluer S, Hallast P, Crepaldi L, Zhou Y, Urgo K, Dincer C, Su J, Noell G, Alasoo K, El Garwany O, Gerety SS, Newman B, Dovey OM, Parts L. Optimized whole-genome CRISPR interference screens identify ARID1A-dependent growth regulators in human induced pluripotent stem cells. Stem Cell Reports. PMID 37028423 DOI: 10.1016/j.stemcr.2023.03.008 |
0.193 |
|
| 2011 |
Putku M, Kepp K, Org E, Sõber S, Comas D, Viigimaa M, Veldre G, Juhanson P, Hallast P, Tõnisson N, Shaw-Hawkins S, Caulfield MJ, Khusnutdinova E, et al. Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans. Human Mutation. 32: 806-14. PMID 21520334 DOI: 10.1002/humu.21508 |
0.134 |
|
| 2019 |
Khubrani YM, Hallast P, Jobling MA, Wetton JH. Massively parallel sequencing of autosomal STRs and identity-informative SNPs highlights consanguinity in Saudi Arabia. Forensic Science International. Genetics. 43: 102164. PMID 31585345 DOI: 10.1016/j.fsigen.2019.102164 |
0.119 |
|
| 2017 |
Batini C, Hallast P, Vågene ÅJ, Zadik D, Eriksen HA, Pamjav H, Sajantila A, Wetton JH, Jobling MA. Population resequencing of European mitochondrial genomes highlights sex-bias in Bronze Age demographic expansions. Scientific Reports. 7: 12086. PMID 28935946 DOI: 10.1038/s41598-017-11307-9 |
0.119 |
|
| 2017 |
Hallast P, Jobling MA. The Y chromosomes of the great apes. Human Genetics. 136: 511-528. PMID 28265767 DOI: 10.1007/s00439-017-1769-8 |
0.119 |
|
| 2017 |
Maisano Delser P, Neumann R, Ballereau S, Hallast P, Batini C, Zadik D, Jobling MA. Signatures of human European Palaeolithic expansion shown by resequencing of non-recombining X-chromosome segments. European Journal of Human Genetics : Ejhg. 25: 485-492. PMID 28120839 DOI: 10.1038/ejhg.2016.207 |
0.119 |
|
| 2013 |
Hallast P, Balaresque P, Bowden GR, Ballereau S, Jobling MA. Recombination dynamics of a human Y-chromosomal palindrome: rapid GC-biased gene conversion, multi-kilobase conversion tracts, and rare inversions. Plos Genetics. 9: e1003666. PMID 23935520 DOI: 10.1371/journal.pgen.1003666 |
0.119 |
|
| 2010 |
Nagirnaja L, Rull K, Uusküla L, Hallast P, Grigorova M, Laan M. Genomics and genetics of gonadotropin beta-subunit genes: Unique FSHB and duplicated LHB/CGB loci. Molecular and Cellular Endocrinology. 329: 4-16. PMID 20488225 DOI: 10.1016/j.mce.2010.04.024 |
0.119 |
|
| 2008 |
Hallast P, Saarela J, Palotie A, Laan M. High divergence in primate-specific duplicated regions: human and chimpanzee chorionic gonadotropin beta genes. Bmc Evolutionary Biology. 8: 195. PMID 18606016 DOI: 10.1186/1471-2148-8-195 |
0.119 |
|
| 2006 |
Hallast P, Rull K, Laan M. The evolution and genomic landscape of CGB1 and CGB2 genes. Molecular and Cellular Endocrinology. 2-11. PMID 17055150 DOI: 10.1016/j.mce.2005.11.049 |
0.119 |
|
| 2006 |
Hallast P, Nagirnaja L, Margus T, Laan M. Segmental duplications and gene conversion: Human luteinizing hormone/chorionic gonadotropin beta gene cluster. Genome Research. 15: 1535-46. PMID 16251463 DOI: 10.1101/gr.4270505 |
0.119 |
|
| 2005 |
Kõks S, Nikopensius T, Koido K, Maron E, Altmäe S, Heinaste E, Vabrit K, Tammekivi V, Hallast P, Kurg A, Shlik J, Vasar V, Metspalu A, Vasar E. Analysis of SNP profiles in patients with major depressive disorder. The International Journal of Neuropsychopharmacology. 9: 167-74. PMID 15927089 DOI: 10.1017/S1461145705005468 |
0.119 |
|
| 2005 |
Maron E, Nikopensius T, Kõks S, Altmäe S, Heinaste E, Vabrit K, Tammekivi V, Hallast P, Koido K, Kurg A, Metspalu A, Vasar E, Vasar V, Shlik J. Association study of 90 candidate gene polymorphisms in panic disorder. Psychiatric Genetics. 15: 17-24. PMID 15722953 DOI: 10.1097/00041444-200503000-00004 |
0.119 |
|
| 2004 |
Koido K, Kõks S, Nikopensius T, Maron E, Altmäe S, Heinaste E, Vabrit K, Tammekivi V, Hallast P, Kurg A, Shlik J, Vasar V, Metspalu A, Vasar E. Polymorphisms in wolframin (WFS1) gene are possibly related to increased risk for mood disorders. The International Journal of Neuropsychopharmacology. 8: 235-44. PMID 15473915 DOI: 10.1017/S1461145704004791 |
0.119 |
|
| Hide low-probability matches. |