about
Mitochondrial DNA and Y chromosome variation provides evidence for a recent common ancestry between Native Americans and Indigenous AltaiansExploring the role of copy number variants in human adaptationAnalysis of variable retroduplications in human populations suggests coupling of retrotransposition to cell divisionOrigins and functional impact of copy number variation in the human genomeLandscape of somatic retrotransposition in human cancersA highly annotated whole-genome sequence of a Korean individual.Primate genome architecture influences structural variation mechanisms and functional consequences.Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and AfricaImpact of constitutional copy number variants on biological pathway evolutionBalancing selection on a regulatory region exhibiting ancient variation that predates human-neandertal divergenceRefinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection.Extensive genetic diversity and substructuring among zebrafish strains revealed through copy number variant analysis.Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.Next-generation sequencing-based detection of germline L1-mediated transductions.Regulatory element copy number differences shape primate expression profiles.The psoriasis-associated deletion of late cornified envelope genes LCE3B and LCE3C has been maintained under balancing selection since Human Denisovan divergence.Global Survey of Variation in a Human Olfactory Receptor Gene Reveals Signatures of Non-Neutral Evolution.Segmental duplications and evolutionary acquisition of UV damage response in the SPATA31 gene family of primates and humans.Recent evolution of the salivary mucin MUC7.Vif proteins from diverse primate lentiviral lineages use the same binding site in APOBEC3GCopy number variants (CNVs) in primate species using array-based comparative genomic hybridization.Geographic distribution and adaptive significance of genomic structural variants: an anthropological genetics perspective.Regulation of lipids is central to replicative senescence.Atopic Dermatitis Susceptibility Variants in Filaggrin Hitchhike Hornerin Selective Sweep.VCFtoTree: a user-friendly tool to construct locus-specific alignments and phylogenies from thousands of anthropologically relevant genome sequences.The evolution and functional impact of human deletion variants shared with archaic hominin genomes.Analysis of somatic retrotransposition in human cancers.Archaic Hominin Introgression in Africa Contributes to Functional Salivary MUC7 Genetic Variation.Variation and functional impact of Neanderthal ancestry in Western Asia.Genetic variation in the enigmatic Altaian Kazakhs of South-Central Russia: insights into Turkic population history.Complex evolution of the GSTM gene family involves sharing of GSTM1 deletion polymorphism in humans and chimpanzees.Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals.An evolutionary transcriptomics approach links CD36 to membrane remodeling in replicative senescenceAn evolutionary transcriptomics approach links CD36 to membrane remodeling in replicative senescenceMitochondrial DNA and Y Chromosome Variation Provides Evidence for a Recent Common Ancestry between Native Americans and Indigenous AltaiansIndependent amylase gene copy number bursts correlate with dietary preferences in mammalsAn Evolutionary Perspective on the Impact of Genomic Copy Number Variation on Human HealthComplex Haplotypes of GSTM1 Gene Deletions Harbor Signatures of a Selective Sweep in East Asian PopulationsHuman and Nonhuman Primate Lineage-Specific Footprints in the Salivary ProteomeArchaic hominin introgression into modern human genomes
P50
Q24633705-13101925-2536-44B7-B077-49C5CF97DAE3Q28263929-A008EB77-CB3A-4A38-AAE7-53793E16DE73Q28661361-4B5D2E2F-CF90-4230-9CE5-512C647737D6Q28730507-2EFB6469-BF6B-4F21-A4BF-91358C2AC56EQ29617664-45CB6AAB-C18B-4ED3-A412-5F3DAF66F2AFQ33815862-70269154-74DE-4542-9693-9893091C8358Q34369514-93041768-096A-4B49-BC05-F98FADEA5115Q34537410-D9404680-4C18-4735-AA45-5B8F3EBCD56AQ34559752-AB0B12D4-1A28-44E5-8D0B-AB5A0840FF3EQ34671949-3EFC34BC-7527-4C41-8F88-A8EDC5F796B2Q35561178-AE691B32-F4DC-4DA0-B3F6-5AAF61EA58B9Q35673740-5980531E-1BA1-4280-9FCD-7D011E02BFCDQ35897714-3307A8F5-24BE-4E63-9D29-766BE67DFAE0Q36012836-AB389226-34AB-434C-A1B4-3C7FA7A3C2C0Q36140248-4E9CB9ED-7741-41F7-8217-4180F19A4B48Q36213630-7669685C-E0D6-403A-9749-789E9EF8ADAAQ36255535-D1C3C615-B126-49FD-B851-CFB9B51D8B1DQ36298683-9F36A032-28AD-4338-A770-F7EA1287F6A5Q37202557-EBA3F768-DBDB-48AE-BEF1-5B898755C2B6Q37252797-9EE4C030-222A-4688-AD06-2BBE0832D62EQ37527167-B438681A-2CCD-4909-B684-079BB9F7BC86Q38470371-E0B01713-D0F7-49C1-B511-63DCF72FD589Q38719185-AB5D6080-458F-4839-B428-C79A92B80770Q39599395-07B7C1CD-3BA6-4463-86D9-0625B2739CB8Q41670301-1330B915-8E9F-4981-8408-5E6958F25FB1Q42092879-39D60952-5095-4CFB-9053-94EDD4C99F82Q45979845-060949FD-AB54-4978-A26A-B21D306E8224Q46299510-E29CF63B-CA06-4297-AF9D-A80249BFEDDCQ46772059-45AA7B0F-92D8-469E-844C-DC4CA768E88EQ47706151-1D382491-116E-455F-8404-EE67F99B2D33Q52309647-1ABC75EA-8E77-4F9B-87B5-8044BD54D9A5Q53417216-33CBEE14-2463-492D-BC3C-D1A7F8787257Q56474400-7D48C950-89F0-4BBF-ACDA-F1DAC24BD34EQ57170623-F5047C0E-D42F-4206-889F-2656536F9110Q59702078-F7ABAF50-B06D-491A-9558-918744E09051Q64055933-939FED16-19A0-4A3F-8F54-CCB05492426CQ90111607-3508AB57-913C-4A9C-BBAE-F17E14CEF672Q90645991-4BFD7B24-5EB9-4334-90C6-78CA8C71156DQ90719700-DD10A390-1232-4274-8BAC-B605007ECB5AQ91183942-DB853ABA-DC80-454D-8C91-3650D69807AD
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Omer Gokcumen
@ast
Omer Gokcumen
@en
Omer Gokcumen
@es
Omer Gokcumen
@nl
type
label
Omer Gokcumen
@ast
Omer Gokcumen
@en
Omer Gokcumen
@es
Omer Gokcumen
@nl
prefLabel
Omer Gokcumen
@ast
Omer Gokcumen
@en
Omer Gokcumen
@es
Omer Gokcumen
@nl
P106
P31
P496
0000-0003-4371-679X