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human-genetics
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human-genetics
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· documents ABOUT human-genetics across the archive
57
Documents about human-genetics
Documents about human-genetics
Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells.
#452345
Lund University Publications
The Genetics of Polycystic Ovarian Syndrome
#848347
ClinicalTrials.gov
Author Correction: A genomic catalog of Earth’s microbiomes
#491753
eScholarship
Differential Gene Expression Associated with Idiopathic Epilepsy in Belgian Shepherd Dogs
#780570
eScholarship
Paradigm Transformation of Global Health Data Regulation: Challenges in Governance and Human Rights Protection of Cross-Border Data Flows
#964864
OpenAlex
Sequencing and functional validation of the JGI Brachypodium distachyon T‐DNA collection
#784324
eScholarship
Position statement from the Italian Society of Human Genetics (SIGU) on the implementation of germline pharmacogenetic testing
#202767
IRIS
AI in variant analysis: fast track to genetic diagnoses
#316797
Springer Nature OA
Consumer Genetic Technologies: Ethical and Legal Considerations
#467900
Duke Law Scholarship Repository
Personalized Genomic Research
#992682
ClinicalTrials.gov
Genome Scanning Reveals the Genetic Basis of a Color Pattern Morphotype in an Island Population of the European Adder (Vipera berus)
#344104
Figshare
Absence of genome reduction in diverse, facultative endohyphal bacteria
#491967
eScholarship
Conserved multi-tissue transcriptomic adaptations to exercise training in humans and mice
#492038
eScholarship
HipMer
#612073
eScholarship
Genomic basis of delayed reward discounting
#620175
eScholarship
Nuclear and Mitochondrial Genome Defects in Autisms
#675868
eScholarship
Pleiotropic genes for metabolic syndrome and inflammation
#784263
eScholarship
Studies of Children With Metabolic and Other Genetic Disorders
#863742
ClinicalTrials.gov
Appearance-related stigma and its implications for genetic counselling practice
#256194
Springer Nature OA
Translational reading frame predicts the pathogenicity of C-terminal frameshift deletions in MeCP2
#669693
Europe PMC
Delineating the early transcriptional specification of the mammalian trachea and esophagus
#609413
eScholarship
Species- and site-specific genome editing in complex bacterial communities
#683847
eScholarship
Parental body mass index and offspring childhood body size and eating behaviour: A structural equation modelling analysis in the Norwegian Mother, Father and Child Cohort Study
#305597
PLOS
HLA-DRB1 and HLA-DQB1 genetic diversity modulates response to lithium in bipolar affective disorders
#346018
UNSWorks Repository
Are minor alleles more likely to be risk alleles?
#491823
eScholarship
Genetic interaction mapping with microfluidic-based single cell sequencing
#609452
eScholarship
Functional Segregation of Overlapping Genes in HIV
#612001
eScholarship
Maintenance of Sympatric and Allopatric Populations in Free-Living Terrestrial Bacteria
#620064
eScholarship
Generation of accurate, expandable phylogenomic trees with uDance
#780569
eScholarship
Our Microbes, Ourselves: Exploring Human-Pathogen Coevolution through the Lens of Ancient DNA
#442614
Harvard DASH
Influence of Genetics on Vitamin Metabolism in Pregnant Women
#832450
ClinicalTrials.gov
Genetic risk for high body mass index before and amidst the obesity epidemic: Cross-cohort analysis of four british birth cohort studies
#292679
PLOS
Precision annotation of digital samples in NCBI’s gene expression omnibus
#491978
eScholarship
A new view of the tree of life
#683988
eScholarship
A simple salting out procedure for extracting DNA from human nucleated cells
#6729
OpenAlex
Comparative genomics of human brain and immune gene preservation across species
#172204
PLOS
Dissecting Human Gene Regulatory Networks with Barcoded CRISPR Screens
#634808
eScholarship
Genetics of COVID-19 Susceptibility and Manifestations
#833232
ClinicalTrials.gov
Study of Clinical and Molecular Manifestations of Genetic Disorders
#916291
ClinicalTrials.gov
A platform for curated products from novel open reading frames prompts reinterpretation of disease variants.
#363412
Apollo
SUMO E3 ligase Mms21 prevents spontaneous DNA damage induced genome rearrangements
#491759
eScholarship
Construction of a map-based reference genome sequence for barley, Hordeum vulgare L.
#491845
eScholarship
L-GIREMI uncovers RNA editing sites in long-read RNA-seq
#492054
eScholarship
SCONCE2: jointly inferring single cell copy number profiles and tumor evolutionary distances
#491862
eScholarship
Diel rewiring and positive selection of ancient plant proteins enabled evolution of CAM photosynthesis in Agave
#492016
eScholarship
Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness
#620085
eScholarship
Association of <i>MDM2</i> rs2279744 and rs937282 polymorphisms with breast cancer susceptibility and circulating <i>MDM2</i> and <i>p53</i> levels in Bangladeshi women: A case-control study
#631447
PLOS
Speciation Genomics in the Tiger Whiptail Lizards (Aspidoscelis tigris Complex)
#634713
eScholarship
ADVANTAGE: Advanced discovery of visceral analgesics by neuroimmune targets and the genetics of extreme human phenotype, a study protocol.
#219145
NCBI PubMed Central
Cell villages and Dirichlet modeling map human cell fitness genetics
#484969
Europe PMC
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