K. McAllister

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New Rodent Population Models May Inform Human Health Risk Assessment and Identification of Genetic Susceptibility to Environmental Exposures

A. Harrill, K. McAllister, 2017, Environmental health perspectives.

Beyond the looking glass: recent advances in understanding the impact of environmental exposures on neuropsychiatric disease

E. Levin, T. Guilarte, C. Ladd-Acosta, 2020, Neuropsychopharmacology.

In Vivo Interactions between Ionizing Radiation, Inflammation and Chemical Carcinogens Identified by Increased DNA Damage Responses

E. Wright, P. Coates, S. Lorimore, 2012, Radiation research.

The Impact of Environmental Factors on Monogenic Mendelian Diseases.

C. Royal, Aaron B. Bowman, Anke M. Tukker, 2021, Toxicological sciences : an official journal of the Society of Toxicology.

Mutant Brca2/p53 mice exhibit altered radiation responses in the developing mammary gland.

S. Peddada, B. Davis, W. Gersch, 2005, Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie.

Are Trp53 rescue of Brca1 embryonic lethality and Trp53/Brca1 breast cancer association related?

R. Wiseman, K. McAllister, 2002, Breast Cancer Research.

Spontaneous and Irradiation-Induced Tumor Susceptibility in Brca2 Germline Mutant Mice and Cooperative Effects with a p53 Germline Mutation

L. Bennett, R. Wiseman, B. Davis, 2006, Toxicologic pathology.

Cancer susceptibility of mice with a homozygous deletion in the COOH-terminal domain of the Brca2 gene.

J. Haseman, L. Bennett, R. Wiseman, 2002, Cancer research.

Advances in Brief Cancer Susceptibility of Mice with a Homozygous Deletion in the COOH-Terminal Domain of the Brca 2 Gene 1

J. Haseman, L. Bennett, R. Wiseman, 2002 .

What about the environment? Leveraging multi-omic datasets to characterize the environment’s role in human health

C. Patel, A. Manrai, Kristin Passero, 2021, Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing.

Thymic model for examining BRCA2 expression and function

R. Wiseman, L. Hale, K. McAllister, 2002, Molecular carcinogenesis.

Environmental Epigenomics, Imprinting and Disease Susceptibility

F. Tyson, J. Heindel, K. McAllister, 2006, Epigenetics.

Brca1 and Brca2 expression patterns in mitotic and meiotic cells of mice

L. Bennett, J. Foley, R. Wiseman, 1998, Oncogene.

A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.

D. W. Johnson, M. Porteous, D. Marchuk, 1995, Genome research.

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

D. W. Johnson, M. Pericak-Vance, A. Guttmacher, 1994, Nature Genetics.

Environmental Health Research in Africa: Important Progress and Promising Opportunities

Bonnie R. Joubert, B. Joubert, K. McAllister, 2020, Frontiers in Genetics.

Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.

M. Pericak-Vance, A. Guttmacher, D. Marchuk, 1994, Journal of medical genetics.

Mitochondria, Energetics, Epigenetics, and Cellular Responses to Stress

Thomas J. Begley, A. Baccarelli, T. Ideker, 2014, Environmental health perspectives.

Mammary Tumor Induction and Premature Ovarian Failure in ApcMin Mice Are Not Enhanced by Brca2 Defi ciency

K A McAllister, L. Bennett, R. Wiseman, 2001, Toxicologic pathology.

Characterization of the rat and mouse homologues of the BRCA2 breast cancer susceptibility gene.

L. Bennett, P. A. Futreal, A. Haugen-Strano, 1997, Cancer research.

Brca2‐Null Embryonic Survival is Prolonged on the BALB/c Genetic Background

R. Wiseman, B. Davis, P. Blackshear, 2000, Molecular Carcinogenesis.

The NIEHS TaRGET II Consortium and environmental epigenomics

David L. Aylor, Erica C. Pehrsson, S. Rajagopalan, 2018, Nature Biotechnology.

Advances in Brief Characterization of the Rat and Mouse Homologues of the BRCA 2 Breast Cancer Susceptibility Gene

A. Haugen-Strano, K. McAllister, H. A. Brownlee, 2006 .

Towards precision prevention: Technologies for identifying healthy individuals with high risk of disease.

J. Bielas, D. Brenner, Q. Wei, 2017, Mutation research.

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

Kathryn Roeder, Peter Kraft, Matthew Stephens, 2012, Genetic epidemiology.

Genetic mapping of the Brca2 breast cancer susceptibility gene on mouse Chromosome 5

S. Ramachandran, A. Haugen-Strano, R. Wiseman, 1997, Mammalian Genome.

Genetic Simulation Tools for Post‐Genome Wide Association Studies of Complex Diseases

Bo Peng, Vineet Bafna, Chun Li, 2015, Genetic epidemiology.

Mice heterozygous for a Brca1 or Brca2 mutation display distinct mammary gland and ovarian phenotypes in response to diethylstilbestrol.

B. Koller, L. Bennett, R. Wiseman, 2000, Cancer research.

Mice Heterozygous for a Brca 1 or Brca 2 Mutation Display Distinct Mammary Gland and Ovarian Phenotypes in Response to Diethylstilbestrol 1

B. Koller, L. Bennett, R. Wiseman, 2000 .

Lessons Learned From Past Gene-Environment Interaction Successes

Peter Kraft, Kimberly McAllister, Nilanjan Chatterjee, 2017, American journal of epidemiology.

Gene‐environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop

Peter Kraft, Kimberly McAllister, Eric Boerwinkle, 2011, Genetic epidemiology.

Integrating environmental health and genomics research in Africa: challenges and opportunities identified during a Human Heredity and Health in Africa (H3Africa) Consortium workshop

K. Berhane, M. Ramsay, B. Joubert, 2019, AAS open research.

Opportunities and Challenges for Environmental Exposure Assessment in Population-Based Studies

Beate Ritz, Jacqueline Kerr, Bhramar Mukherjee, 2017, Cancer Epidemiology, Biomarkers & Prevention.

Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex Diseases.

Bhramar Mukherjee, Peng Wei, Kimberly McAllister, 2017, American journal of epidemiology.

Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1.

J. Surrallés, S. Puerto, J. Segovia, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles

Joshua D. Smith, A. Guttmacher, W. Craigen, 1998, Human mutation.

Introduction to mammalian genome special issue: the combined role of genetics and environment relevant to human disease outcomes

K. Svenson, I. Rusyn, J. French, 2018, Mammalian Genome.

Expanding the Concept of Translational Research: Making a Place for Environmental Health Sciences

Kristianna G. Pettibone, A. R. Latoni, N. Walker, 2018, Environmental health perspectives.

Six novel mutations in the endoglin gene in hereditary hemorrhagic telangiectasia type 1 suggest a dominant-negative effect of receptor function.

A. Guttmacher, M. Porteous, D. Marchuk, 1995, Human molecular genetics.

What about the environment? Leveraging multi-omic datasets to characterize the environment's role in human health

Kimberly McAllister, Chirag J. Patel, Molly A. Hall, 2020, PSB.

COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type II.

D. Kwiatkowski, D. Marchuk, D. Greenspan, 1995, Genomics.

Meeting report: Identification of biomarkers for early detection of mitochondrial dysfunction.

C. Lawler, W. Copeland, M. Longley, 2010, Mitochondrion (Amsterdam. Print).

Extragonadal Teratocarcinoma in Chimeric Mice

L. Bennett, B. Davis, P. Blackshear, 1999, Veterinary Pathology-Supplement.