Kirk E. Lohmueller

researcher

Kirk E. Lohmueller is …
instance of (P31):
humanQ5

External links are
P2381Academic Tree ID189241
P8214curriculum vitae URLhttps://faculty.eeb.ucla.edu/Lohmueller/data/uploads/lohmueller_cv_academic_november.27.2019.pdf
P1960Google Scholar author IDc_hM9mAAAAAJ
P244Library of Congress authority IDn2022182613
P856official websitehttps://faculty.eeb.ucla.edu/Lohmueller/
P496ORCID iD0000-0002-3874-369X
P214VIAF ID21165746545953930657

P8413academic appointmentUCLA Department of Ecology and Evolutionary BiologyQ105299200
P184doctoral advisorAndrew G. ClarkQ4757042
Carlos D. BustamanteQ17612152
P185doctoral studentJazlyn MooneyQ92172491
P69educated atCornell UniversityQ49115
Georgetown UniversityQ333886
P108employerUniversity of California, Los AngelesQ174710
P101field of workpopulation geneticsQ31151
genomicsQ222046
P106occupationuniversity teacherQ1622272
academicQ3400985
P5008on focus list of Wikimedia projectWikiProject PCC Wikidata Pilot/UCLAQ100999455
P803professorshipassociate professorQ9344260
P21sex or gendermaleQ6581097

Reverse relations

doctoral student (P185)
Q4757042Andrew G. Clark
Q17612152Carlos D. Bustamante

author (P50)
Q96644597A community-maintained standard library of population genetic models
Q22337119A comprehensive review of genetic association studies
Q30000667A model-based approach for identifying signatures of ancient balancing selection in genetic data
Q28290486A simple genetic architecture underlies morphological variation in dogs
Q33772642Amerindian-specific regions under positive selection harbour new lipid variants in Latinos
Q28659864An Aboriginal Australian genome reveals separate human dispersals into Asia
Q40018142An assessment of the information content of likelihood ratios derived from complex mixtures
Q51084583Analysis of allelic drop-out using the Identifiler(®) and PowerPlex(®) 16 forensic STR typing systems.
Q30840823Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping
Q92850987Aquatic Adaptation and Depleted Diversity: A Deep Dive into the Genomes of the Sea Otter and Giant Otter
Q33339383Assessing the evolutionary impact of amino acid mutations in the human genome
Q34506401Bottlenecks and selective sweeps during domestication have increased deleterious genetic variation in dogs
Q47277823Calculating the weight of evidence in low-template forensic DNA casework.
Q46959041Comparison of Single Genome and Allele Frequency Data Reveals Discordant Demographic Histories.
Q92194457Complex patterns of sex-biased demography in canines
Q57805334Deleterious variation shapes the genomic landscape of introgression
Q22066006Detecting ancient admixture and estimating demographic parameters in multiple human populations
Q34714977Detecting directional selection in the presence of recent admixture in African-Americans
Q36100045Determining the Effect of Natural Selection on Linked Neutral Divergence across Species
Q33620151Determining the factors driving selective effects of new nonsynonymous mutations
Q33929681Estimation of allele frequency and association mapping using next-generation sequencing data
Q46002261Evolution. On the origin of Peter Rabbit.
Q29040619Evolutionary History, Selective Sweeps, and Deleterious Variation in the Dog
Q46186272Fitting the Balding-Nichols model to forensic databases
Q61136551Gene expression drives the evolution of dominance
Q24615541Genome-wide SNP and haplotype analyses reveal a rich history underlying dog domestication
Q39823767Genomic Flatlining in the Endangered Island Fox.
Q115037682Genomic analyses reveal range‐wide devastation of sea otter populations
Q39629179Genomic divergence across ecological gradients in the Central African rainforest songbird (Andropadus virens).
Q57213176Genomic history of the Sardinian population
Q64290595Genomic signatures of extensive inbreeding in Isle Royale wolves, a population on the threshold of extinction
Q24651979Global distribution of genomic diversity underscores rich complex history of continental human populations
Q84196991Graydon et al. provide no new evidence that forensic STR loci are functional
Q102151685Greater strength of selection and higher proportion of beneficial amino acid changing mutations in humans compared to mice and Drosophila melanogaster
Q59134746Growth factor gene IGF1 is associated with bill size in the black-bellied seedcracker Pyrenestes ostrinus
Q36232888Height-reducing variants and selection for short stature in Sardinia
Q112278394High-quality genome and methylomes illustrate features underlying evolutionary success of oaks
Q103836712Identification and characterization of constrained non-exonic bases lacking predictive epigenomic and transcription factor binding annotations
Q33642802Inference of the Distribution of Selection Coefficients for New Nonsynonymous Mutations Using Large Samples
Q35780760Lab Retriever: a software tool for calculating likelihood ratios incorporating a probability of drop-out for forensic DNA profiles
Q36695811Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders
Q117215712MaLAdapt Reveals Novel Targets of Adaptive Introgression From Neanderthals and Denisovans in Worldwide Human Populations
Q22337234Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
Q22337164Methods for high-density admixture mapping of disease genes
Q33414073Methods for human demographic inference using haplotype patterns from genomewide single-nucleotide polymorphism data
Q52567199Natural Selection and Origin of a Melanistic Allele in North American Gray Wolves.
Q34055381Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome.
Q37458166Natural selection reduced diversity on human y chromosomes
Q115223215Negative selection on complex traits limits phenotype prediction accuracy between populations
Q39582587PReFerSim: fast simulation of demography and selection under the Poisson Random Field model
Q112728610Patterns of de novo tandem repeat mutations and their role in autism
Q95943072Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution
Q30367885Proportionally more deleterious genetic variation in European than in African populations.
Q92981260Purging of Strongly Deleterious Mutations Explains Long-Term Persistence and Absence of Inbreeding Depression in Island Foxes
Q91502209RADseq data reveal ancient, but not pervasive, introgression between Californian tree and scrub oak species (Quercus sect. Quercus: Fagaceae)
Q34462822Selection and reduced population size cannot explain higher amounts of Neandertal ancestry in East Asian than in European human populations
Q42587388Sex-averaged recombination and mutation rates on the X chromosome: a comment on Labuda et al.
Q92172498Ten simple rules for giving an effective academic job talk
Q90507600Testing whether stutter and low-level DNA peaks are additive
Q46545285The Effect of an Extreme and Prolonged Population Bottleneck on Patterns of Deleterious Variation: Insights from the Greenlandic Inuit
Q96124326The Impact of Recessive Deleterious Variation on Signals of Adaptive Introgression in Human Populations
Q114142880The critically endangered vaquita is not doomed to extinction by inbreeding depression
Q38280771The distribution of deleterious genetic variation in human populations
Q33895392The effect of recent admixture on inference of ancient human population history
Q33686100The impact of population demography and selection on the genetic architecture of complex traits
Q58618781Understanding the Hidden Complexity of Latin American Population Isolates
Q45173031Validation of probabilistic genotyping software for use in forensic DNA casework: Definitions and illustrations
Q34398712Variants associated with common disease are not unusually differentiated in frequency across populations
Q55434799Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes
Q37367893Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes

Q92172491Jazlyn Mooneydoctoral advisorP184

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