List of works - Lora Lewis

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies ⬇️

scientific article

A high-resolution map of human evolutionary constraint using 29 mammals

scientific article

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

scientific article

Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients

article

Comprehensive Characterization of Cancer Driver Genes and Mutations

article

Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma

scientific article published on 4 November 2015

Evolutionary and Biomedical Insights from the Rhesus Macaque Genome

scientific article

Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy

scientific article

Functional and evolutionary insights from the genomes of three parasitoid Nasonia species

scientific article

Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development

scientific article

Genome sequence of the Brown Norway rat yields insights into mammalian evolution

scientific article

Germline mutations in shelterin complex genes are associated with familial glioma

scientific article

Gibbon genome and the fast karyotype evolution of small apes

scientific article

Hemichordate genomes and deuterostome origins

scientific article

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

scientific article

Integrating common and rare genetic variation in diverse human populations

scientific article (publication date: 2 September 2010)

Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators

scientific article

Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines

scientific article

Novel somatic and germline mutations in intracranial germ cell tumours.

scientific article

Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders

scientific article

Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

scientific article

Patterns and rates of exonic de novo mutations in autism spectrum disorders

scientific article

Somatic mutations affect key pathways in lung adenocarcinoma

scientific article

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

scientific article

The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

article

The DNA sequence of the human X chromosome

scientific article published on 17 March 2005

The DNA sequence, annotation and analysis of human chromosome 3

scientific article (publication date: 27 April 2006)

The finished DNA sequence of human chromosome 12

scientific article

The genome of the model beetle and pest Tribolium castaneum

scientific article

The genome of the sea urchin Strongylocentrotus purpuratus

scientific article

The genome sequence of taurine cattle: a window to ruminant biology and evolution

scientific article

List of works by Lora Lewis

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies ⬇️

A high-resolution map of human evolutionary constraint using 29 mammals

Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls

Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients

Comprehensive Characterization of Cancer Driver Genes and Mutations

Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma

Evolutionary and Biomedical Insights from the Rhesus Macaque Genome

Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy

Functional and evolutionary insights from the genomes of three parasitoid Nasonia species

Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development

Genome sequence of the Brown Norway rat yields insights into mammalian evolution

Germline mutations in shelterin complex genes are associated with familial glioma

Gibbon genome and the fast karyotype evolution of small apes

Hemichordate genomes and deuterostome origins

Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes

Integrating common and rare genetic variation in diverse human populations

Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators

Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines

Novel somatic and germline mutations in intracranial germ cell tumours.

Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders

Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Somatic mutations affect key pathways in lung adenocarcinoma

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

The DNA sequence of the human X chromosome

The DNA sequence, annotation and analysis of human chromosome 3

The finished DNA sequence of human chromosome 12

The genome of the model beetle and pest Tribolium castaneum

The genome of the sea urchin Strongylocentrotus purpuratus

The genome sequence of taurine cattle: a window to ruminant biology and evolution