human | Q5 |
P2381 | Academic Tree ID | 189241 |
P8214 | curriculum vitae URL | https://faculty.eeb.ucla.edu/Lohmueller/data/uploads/lohmueller_cv_academic_november.27.2019.pdf |
P1960 | Google Scholar author ID | c_hM9mAAAAAJ |
P244 | Library of Congress authority ID | n2022182613 |
P856 | official website | https://faculty.eeb.ucla.edu/Lohmueller/ |
P496 | ORCID iD | 0000-0002-3874-369X |
P214 | VIAF ID | 21165746545953930657 |
P8413 | academic appointment | UCLA Department of Ecology and Evolutionary Biology | Q105299200 |
P184 | doctoral advisor | Andrew G. Clark | Q4757042 |
Carlos D. Bustamante | Q17612152 | ||
P185 | doctoral student | Jazlyn Mooney | Q92172491 |
P69 | educated at | Cornell University | Q49115 |
Georgetown University | Q333886 | ||
P108 | employer | University of California, Los Angeles | Q174710 |
P101 | field of work | population genetics | Q31151 |
genomics | Q222046 | ||
P106 | occupation | university teacher | Q1622272 |
academic | Q3400985 | ||
P5008 | on focus list of Wikimedia project | WikiProject PCC Wikidata Pilot/UCLA | Q100999455 |
P803 | professorship | associate professor | Q9344260 |
P21 | sex or gender | male | Q6581097 |
Q96644597 | A community-maintained standard library of population genetic models |
Q22337119 | A comprehensive review of genetic association studies |
Q30000667 | A model-based approach for identifying signatures of ancient balancing selection in genetic data |
Q28290486 | A simple genetic architecture underlies morphological variation in dogs |
Q33772642 | Amerindian-specific regions under positive selection harbour new lipid variants in Latinos |
Q28659864 | An Aboriginal Australian genome reveals separate human dispersals into Asia |
Q40018142 | An assessment of the information content of likelihood ratios derived from complex mixtures |
Q51084583 | Analysis of allelic drop-out using the Identifiler(®) and PowerPlex(®) 16 forensic STR typing systems. |
Q30840823 | Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping |
Q92850987 | Aquatic Adaptation and Depleted Diversity: A Deep Dive into the Genomes of the Sea Otter and Giant Otter |
Q33339383 | Assessing the evolutionary impact of amino acid mutations in the human genome |
Q34506401 | Bottlenecks and selective sweeps during domestication have increased deleterious genetic variation in dogs |
Q47277823 | Calculating the weight of evidence in low-template forensic DNA casework. |
Q46959041 | Comparison of Single Genome and Allele Frequency Data Reveals Discordant Demographic Histories. |
Q92194457 | Complex patterns of sex-biased demography in canines |
Q57805334 | Deleterious variation shapes the genomic landscape of introgression |
Q22066006 | Detecting ancient admixture and estimating demographic parameters in multiple human populations |
Q34714977 | Detecting directional selection in the presence of recent admixture in African-Americans |
Q36100045 | Determining the Effect of Natural Selection on Linked Neutral Divergence across Species |
Q33620151 | Determining the factors driving selective effects of new nonsynonymous mutations |
Q33929681 | Estimation of allele frequency and association mapping using next-generation sequencing data |
Q46002261 | Evolution. On the origin of Peter Rabbit. |
Q29040619 | Evolutionary History, Selective Sweeps, and Deleterious Variation in the Dog |
Q46186272 | Fitting the Balding-Nichols model to forensic databases |
Q61136551 | Gene expression drives the evolution of dominance |
Q24615541 | Genome-wide SNP and haplotype analyses reveal a rich history underlying dog domestication |
Q39823767 | Genomic Flatlining in the Endangered Island Fox. |
Q115037682 | Genomic analyses reveal range‐wide devastation of sea otter populations |
Q39629179 | Genomic divergence across ecological gradients in the Central African rainforest songbird (Andropadus virens). |
Q57213176 | Genomic history of the Sardinian population |
Q64290595 | Genomic signatures of extensive inbreeding in Isle Royale wolves, a population on the threshold of extinction |
Q24651979 | Global distribution of genomic diversity underscores rich complex history of continental human populations |
Q84196991 | Graydon et al. provide no new evidence that forensic STR loci are functional |
Q102151685 | Greater strength of selection and higher proportion of beneficial amino acid changing mutations in humans compared to mice and Drosophila melanogaster |
Q59134746 | Growth factor gene IGF1 is associated with bill size in the black-bellied seedcracker Pyrenestes ostrinus |
Q36232888 | Height-reducing variants and selection for short stature in Sardinia |
Q112278394 | High-quality genome and methylomes illustrate features underlying evolutionary success of oaks |
Q103836712 | Identification and characterization of constrained non-exonic bases lacking predictive epigenomic and transcription factor binding annotations |
Q33642802 | Inference of the Distribution of Selection Coefficients for New Nonsynonymous Mutations Using Large Samples |
Q35780760 | Lab Retriever: a software tool for calculating likelihood ratios incorporating a probability of drop-out for forensic DNA profiles |
Q36695811 | Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders |
Q117215712 | MaLAdapt Reveals Novel Targets of Adaptive Introgression From Neanderthals and Denisovans in Worldwide Human Populations |
Q22337234 | Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease |
Q22337164 | Methods for high-density admixture mapping of disease genes |
Q33414073 | Methods for human demographic inference using haplotype patterns from genomewide single-nucleotide polymorphism data |
Q52567199 | Natural Selection and Origin of a Melanistic Allele in North American Gray Wolves. |
Q34055381 | Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genome. |
Q37458166 | Natural selection reduced diversity on human y chromosomes |
Q115223215 | Negative selection on complex traits limits phenotype prediction accuracy between populations |
Q39582587 | PReFerSim: fast simulation of demography and selection under the Poisson Random Field model |
Q112728610 | Patterns of de novo tandem repeat mutations and their role in autism |
Q95943072 | Population genetic models of GERP scores suggest pervasive turnover of constrained sites across mammalian evolution |
Q30367885 | Proportionally more deleterious genetic variation in European than in African populations. |
Q92981260 | Purging of Strongly Deleterious Mutations Explains Long-Term Persistence and Absence of Inbreeding Depression in Island Foxes |
Q91502209 | RADseq data reveal ancient, but not pervasive, introgression between Californian tree and scrub oak species (Quercus sect. Quercus: Fagaceae) |
Q34462822 | Selection and reduced population size cannot explain higher amounts of Neandertal ancestry in East Asian than in European human populations |
Q42587388 | Sex-averaged recombination and mutation rates on the X chromosome: a comment on Labuda et al. |
Q92172498 | Ten simple rules for giving an effective academic job talk |
Q90507600 | Testing whether stutter and low-level DNA peaks are additive |
Q46545285 | The Effect of an Extreme and Prolonged Population Bottleneck on Patterns of Deleterious Variation: Insights from the Greenlandic Inuit |
Q96124326 | The Impact of Recessive Deleterious Variation on Signals of Adaptive Introgression in Human Populations |
Q114142880 | The critically endangered vaquita is not doomed to extinction by inbreeding depression |
Q38280771 | The distribution of deleterious genetic variation in human populations |
Q33895392 | The effect of recent admixture on inference of ancient human population history |
Q33686100 | The impact of population demography and selection on the genetic architecture of complex traits |
Q58618781 | Understanding the Hidden Complexity of Latin American Population Isolates |
Q45173031 | Validation of probabilistic genotyping software for use in forensic DNA casework: Definitions and illustrations |
Q34398712 | Variants associated with common disease are not unusually differentiated in frequency across populations |
Q55434799 | Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes |
Q37367893 | Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes |
Q92172491 | Jazlyn Mooney | doctoral advisor | P184 |
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