human | Q5 |
P8079 | elibrary.ru person ID | 80768 |
P2671 | Google Knowledge Graph ID | /g/119pfjwtf |
P244 | Library of Congress authority ID | n2002111513 |
P496 | ORCID iD | 0000-0003-2987-3334 |
P3829 | Publons author ID | 2679638 |
P1053 | ResearcherID | A-4810-2013 |
P214 | VIAF ID | 41206803 |
P512 | academic degree | Doktor Nauk in Biology | Q17281188 |
P166 | award received | Merited Scientist of the Russian Federation | Q4187996 |
Merited Scientist of the Republic of Bashkortostan | Q56062992 | ||
P27 | country of citizenship | Russia | Q159 |
Soviet Union | Q15180 | ||
P69 | educated at | Bashkir State University | Q906235 |
P108 | employer | Bashkir State University | Q906235 |
Bashkir State Medical University | Q4080165 | ||
Bashkir State Pedagogical University | Q4080166 | ||
P22 | father | ??? | Q12079805 |
P101 | field of work | genetics | Q7162 |
population genetics | Q31151 | ||
P735 | given name | Elsa | Q1077181 |
Elsa | Q1077181 | ||
P1412 | languages spoken, written or signed | Russian | Q7737 |
P1559 | name in native language | Эльза Камил ҡыҙы Хуснутдинова | |
P106 | occupation | geneticist | Q3126128 |
P551 | residence | Zorge Street | Q4473810 |
P21 | sex or gender | female | Q6581072 |
P26 | spouse | ??? | Q119702449 |
Q36016386 | 11q13 is a susceptibility locus for hormone receptor positive breast cancer |
Q37169873 | 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium |
Q28554199 | A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics |
Q64948510 | A Splice Site Variant of CDK12 and Breast Cancer in Three Eurasian Populations. |
Q28277415 | A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe |
Q24622032 | A major Y-chromosome haplogroup R1b Holocene era founder effect in Central and Western Europe |
Q47633355 | A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease |
Q59237589 | A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer |
Q48167116 | A rare event of insertion polymorphism of a HERV-K LTR in the human genome |
Q28258830 | A recent bottleneck of Y chromosome diversity coincides with a global change in culture |
Q57305942 | A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer |
Q59237657 | ALU Insertion Polymorphisms in Populations of the South Caucasus |
Q39437211 | Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers |
Q30435992 | Age-Related Hearing Impairment (ARHI) associated with GJB2 single mutation IVS1+1G>A in the Yakut population isolate in Eastern Siberia |
Q59237594 | An STR database on the Volga-Ural population |
Q50693060 | Analysis of CCR5Delta32 geographic distribution and its correlation with some climatic and geographic factors. |
Q59237463 | Analysis of COL1A1 and COL1A2 genes in osteogenesis imperfecta patients from Russia |
Q39578535 | Analysis of genetic variants of class II cytokine and their receptor genes in psoriasis patients of two ethnic groups from the Volga-Ural region of Russia |
Q21534937 | Ancient human genomes suggest three ancestral populations for present-day Europeans |
Q55920422 | Ancient human genomes suggest three ancestral populations for present-day Europeans |
Q40381692 | Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer |
Q28727687 | Assessment of gene-by-sex interaction effect on bone mineral density |
Q45979098 | Association analysis identifies 65 new breast cancer risk loci. |
Q57783938 | Association of Kallikrein Gene Polymorphisms With Intracranial Aneurysms |
Q59237365 | Associations between Vitamin D-Binding Protein (DBP) Gene Polymorphism (TAAA)n and Development of Osteoporosis in the Volga-Ural Region of Russia |
Q35532898 | Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium |
Q57056093 | Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis |
Q24606584 | Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia |
Q46379359 | Autosomal recessive deafness 1A (DFNB1A) in Yakut population isolate in Eastern Siberia: extensive accumulation of the splice site mutation IVS1+1G>A in GJB2 gene as a result of founder effect |
Q21092238 | Beringian standstill and spread of Native American founders |
Q28655316 | Bioethical issues of preventing hereditary diseases with late onset in the Sakha Republic (Yakutia) |
Q48598900 | Brain derived neurotrophic factor gene (BDNF) and personality traits: the modifying effect of season of birth and sex. |
Q41016403 | Brain neurotransmitter systems gene Polymorphism: the Search for pharmacogenetic markers of efficacy of haloperidol in Russians and Tatars |
Q57060722 | Branched-Chain Amino Acid Database Integrated in MEDIPAD Software as a Tool for Nutritional Investigation of Mediterranean Populations |
Q100457582 | Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk |
Q34327945 | Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2 |
Q34622800 | Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia. |
Q31082788 | Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
Q21090943 | Complete mitochondrial DNA analysis of eastern Eurasian haplogroups rarely found in populations of northern Asia and eastern Europe |
Q34181322 | Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer |
Q42320992 | Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics |
Q57278898 | Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
Q101216461 | Cross-cancer genome-wide association study of endometrial cancer and epithelial ovarian cancer identifies genetic risk regions associated with risk of both cancers |
Q24649750 | Decreased rate of evolution in Y chromosome STR loci of increased size of the repeat unit |
Q97418674 | Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third |
Q28266672 | Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus |
Q24643918 | Distribution of the alcohol dehydrogenase ADH1B*47His allele in Eurasia |
Q34333475 | Disuniting uniformity: a pied cladistic canvas of mtDNA haplogroup H in Eurasia |
Q48013111 | Diversity of Y-chromosomal and mtDNA Markers Included in Mediscope Chip within Two Albanian Subpopulations from Croatia and Kosovo: Preliminary Data |
Q36084254 | East Eurasian ancestry in the middle of Europe: genetic footprints of Steppe nomads in the genomes of Belarusian Lipka Tatars |
Q45011870 | Ethnic differences in the serotonin transporter polymorphism (5-HTTLPR) in several European populations |
Q61230414 | Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes |
Q92480972 | Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes |
Q64120953 | Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation |
Q47875710 | From East to West: patterns of genetic diversity of populations living in four Eurasian regions. |
Q114182808 | Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element |
Q47290653 | Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder |
Q30991150 | Genetic Heritage of the Balto-Slavic Speaking Populations: A Synthesis of Autosomal, Mitochondrial and Y-Chromosomal Data |
Q37739048 | Genetic modifiers of CHEK2*1100delC-associated breast cancer risk |
Q55043065 | Genetic structure of Dagestan populations: a study of 11 Alu insertion polymorphisms. |
Q28388497 | Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types |
Q37347628 | Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder |
Q36842233 | Genome-wide association analysis identifies three new breast cancer susceptibility loci |
Q63681757 | Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer |
Q95329367 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses |
Q64040390 | Genome-wide association study of germline variants and breast cancer-specific mortality |
Q28235753 | Genome-wide association study reveals two new risk loci for bipolar disorder |
Q34268288 | Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture |
Q28314885 | Genomic analyses inform on migration events during the peopling of Eurasia |
Q96432094 | Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk |
Q114182677 | Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis |
Q36055779 | Global diversity, population stratification, and selection of human copy-number variation |
Q28596543 | Human Y Chromosome Haplogroup N: A Non-trivial Time-Resolved Phylogeography that Cuts across Language Families |
Q39431978 | Identification of a new locus at 16q12 associated with time to asthma onset |
Q36086247 | Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus |
Q36271840 | Identification of shared risk loci and pathways for bipolar disorder and schizophrenia |
Q46103372 | Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer |
Q59237482 | M06 Epidemiology of Huntington's disease in the Republic of Bashkortostan |
Q111660895 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia |
Q114182490 | Mendelian randomisation study of smoking exposure in relation to breast cancer risk |
Q24682875 | Mitochondrial DNA variation of modern Tuscans supports the near eastern origin of Etruscans |
Q28242469 | Mitochondrial DNA variations in Russian and Belorussian populations |
Q47218106 | Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. |
Q37499453 | Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer |
Q37356243 | Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. |
Q47847793 | Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom's syndrome, is associated with breast cancer in Slavic populations |
Q102322087 | Novel MicroRNA Binding Site SNPs and the Risk of Clear Cell Renal Cell Carcinoma (ccRCC): A Case-Control Study |
Q35818964 | Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans |
Q24532226 | Origin and diffusion of mtDNA haplogroup X |
Q34581051 | Origin and expansion of haplogroup H, the dominant human mitochondrial DNA lineage in West Eurasia: the Near Eastern and Caucasian perspective. |
Q37741283 | Origin and spread of human mitochondrial DNA haplogroup U7. |
Q59237718 | P.1.07 Methylenetetrahydrofolate reductase gene and unipolar depression: focus on personality traits |
Q59237768 | P.1.a.003 The serotonin transporter gene: association with different psychiatric disorders |
Q59237692 | P.1.a.018 The influence of 5-HTT, DRD2, DAT1 and NET genes on personality traits is modified by gene – environment interaction |
Q59237714 | P.1.a.020 DRD4 gene polymorphisms and their influence on personality traits |
Q59237668 | P.2.b.001 Contribution of some serotonergic system genes to suicidal behaviour in Russian population: gender specific association |
Q28601702 | POPULATION GENETICS. Genomic evidence for the Pleistocene and recent population history of Native Americans |
Q24533494 | Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europe |
Q62583133 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes |
Q59238026 | Polymorphism of MET and D7S23 Loci Linked to the Cystic Fibrosis Gene in Bashkir and Komi Populations |
Q59237939 | Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations |
Q58135557 | Polymorphisms at locus D1S80 and other hypervariable regions in the analysis of Eastern European ethnic group relationships |
Q36583004 | Prediction of breast cancer risk based on profiling with common genetic variants |
Q44242400 | Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe |
Q51116126 | Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe. |
Q90242034 | Publisher Correction: Shared heritability and functional enrichment across six solid cancers |
Q46760859 | Rare occurrence of PALB2 mutations in ovarian cancer patients from the Volga-Ural region |
Q37300024 | Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042. |
Q24598410 | Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a |
Q45801075 | Separating the post-Glacial coancestry of European and Asian Y chromosomes within haplogroup R1a. |
Q61118451 | Shared heritability and functional enrichment across six solid cancers |
Q64004349 | Shared heritability and functional enrichment across six solid cancers |
Q91863019 | Shifts in the Genetic Landscape of the Western Eurasian Steppe Associated with the Beginning and End of the Scythian Dominance |
Q28552418 | Spectrum and Frequency of the GJB2 Gene Pathogenic Variants in a Large Cohort of Patients with Hearing Impairment Living in a Subarctic Region of Russia (the Sakha Republic) |
Q59237315 | Stereoselective synthesis of 11-phenylundeca-5Z,9Z-dienoic acid and investigation of its human topoisomerase I and IIα inhibitory activity |
Q104614740 | Structural Variability, Expression Profile, and Pharmacogenetic Properties of TMPRSS2 Gene as a Potential Target for COVID-19 Therapy |
Q59237399 | Synthesis and cytotoxicity of allobetulin derivatives |
Q28248010 | The Caucasus as an asymmetric semipermeable barrier to ancient human migrations |
Q91178389 | The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer |
Q56270968 | The Genetic Legacy of the Expansion of Turkic-Speaking Nomads Across Eurasia |
Q27025297 | The Simons Genome Diversity Project: 300 genomes from 142 diverse populations |
Q47793496 | The facile synthesis of the 5Z,9Z-dienoic acids and their topoisomerase I inhibitory activity. |
Q35514258 | The genetic legacy of the expansion of Turkic-speaking nomads across Eurasia |
Q29606641 | The genetic prehistory of the New World Arctic |
Q28284600 | The genome-wide structure of the Jewish people |
Q34412008 | The phylogenetic and geographic structure of Y-chromosome haplogroup R1a |
Q45201727 | The role of dopamine transporter (SLC6A3) and dopamine D2 receptor/ankyrin repeat and kinase domain containing 1 (DRD2/ANKK1) gene polymorphisms in personality traits |
Q44657483 | The role of inflammatory chemokines in lymphoid neoorganogenesis in breast cancer |
Q51781622 | The serotonin transporter gene: polymorphism and haplotype analysis in Russian suicide attempters. |
Q51671722 | The study of filaggrin gene mutations and copy number variation in atopic dermatitis patients from Volga-Ural region of Russia. |
Q24533322 | The western and eastern roots of the Saami--the story of genetic "outliers" told by mitochondrial DNA and Y chromosomes |
Q89961489 | Transcriptome-wide association study of breast cancer risk by estrogen-receptor status |
Q92994868 | Two truncating variants in FANCC and breast cancer risk |
Q24562029 | Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans |
Q59238022 | Use of DNA fingerprinting for human population genetic studies |
Q42645420 | X-chromosome as a marker for population history: linkage disequilibrium and haplotype study in Eurasian populations |
Q64004908 | Y-chromosomal analysis of clan structure of Kalmyks, the only European Mongol people, and their relationship to Oirat-Mongols of Inner Asia |
Q92282730 | Y-chromosomal connection between Hungarians and geographically distant populations of the Ural Mountain region and West Siberia |
Q12079805 | Камиль Шаехмурзинович Ахияров | child | P40 |
ba | Хөснөтдинова Эльза Камил ҡыҙы | wikipedia |
Elsa Kamilewna Chusnutdinowa | wikipedia | |
Хуснутдинова, Эльза Камилевна | wikipedia | |
Tatar language (tt / Q25285) | Эльза Хөснетдинова | wikipedia |
Хуснутдінова Ельза Камілівна | wikipedia |
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