V. Zismann

发表

A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.

Rebecca F. Halperin, D. Stephan, A. Myers, 2007, The Journal of clinical psychiatry.

GAB2 Alleles Modify Alzheimer's Risk in APOE ɛ4 Carriers

Winnie S. Liang, G. Alexander, D. Stephan, 2007, Neuron.

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.

Winnie S. Liang, G. Alexander, D. Stephan, 2007, Neuron.

Genetic control of human brain transcript expression in Alzheimer disease.

D. Stephan, P. Holmans, A. Myers, 2009, American journal of human genetics.

Canine osteosarcoma genome sequencing identifies recurrent mutations in DMD and the histone methyltransferase gene SETD2

J. Trent, P. Houghton, V. Zismann, 2019, Communications Biology.

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies.

Rebecca F. Halperin, Nils Homer, D. Stephan, 2007, American journal of human genetics.

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

K. Brown, J. Trent, D. Bishop, 2011, Nature.

Frequent somatic MAP3K5 and MAP3K9 mutations in metastatic melanoma identified by exome sequencing

R. Gibbs, K. Brown, J. Trent, 2011, Nature Genetics.

Evidence for an association between KIBRA and late-onset Alzheimer's disease

Richard J. Caselli, Gene E. Alexander, Daniel Bandy, 2010, Neurobiology of Aging.

Identification of disease causing loci using an array-based genotyping approach on pooled DNA

David W Craig, D. Stephan, D. Craig, 2005, BMC Genomics.

Phylogenetic analyses of the ITS region of ribosomal DNA reveal that Septoria passerinii from barley is closely related to the wheat pathogen Mycosphaerella graminicola

V. Zismann, S. B. Goodwin, 2001 .

Integrated genomic analyses reveal frequent TERT aberrations in acral melanoma.

Rebecca F. Halperin, Winnie S. Liang, J. Carpten, 2017, Genome research.

A Universal Day Zero Infectious Disease Testing Strategy Leveraging CRISPR-based Sample Depletion and Metagenomic Sequencing

Y. Hakak, A. Chan, V. Zismann, 2022, medRxiv.

Genomic landscapes of canine splenic angiosarcoma (hemangiosarcoma) contain extensive heterogeneity within and between patients

Rebecca F. Halperin, J. Trent, V. Zismann, 2020, bioRxiv.

Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis.

D. Stephan, S. Melquist, A. Myers, 2010, International journal of molecular epidemiology and genetics.

SNP-based chromosomal copy number ascertainment following multiple displacement whole-genome amplification.

Jason J. Corneveaux, D. Stephan, D. Craig, 2007, BioTechniques.

Polymerase chain reaction for antigen receptor rearrangement: Benchmarking performance of a lymphoid clonality assay in diverse canine sample types

V. Zismann, W. Hendricks, C. Khanna, 2019, Journal of Veterinary Internal Medicine.

A survey of genetic human cortical gene expression

D. Stephan, P. Holmans, A. Myers, 2007, Nature Genetics.

The sequence of rice chromosomes 11 and 12, rich in disease resistance genes and recent gene duplications

Saurabh Raghuvanshi, Joachim Messing, Rod A Wing, 2005, BMC Biology.

Identiﬁcation of a Novel Risk Locus for Progressive Supranuclear Palsy by a Pooled Genomewide Scan of 500,288 Single-Nucleotide Polymorphisms

Jason J. Corneveaux, D. Stephan, S. Melquist, 2007 .

Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

Richard J Caselli, John V Pearson, Irene Litvan, 2007, American journal of human genetics.

Phylogenetic analysis of cercospora and mycosphaerella based on the internal transcribed spacer region of ribosomal DNA.

V. Zismann, S. B. Goodwin, L. Dunkle, 2001, Phytopathology.

Somatic inactivating PTPRJ mutations and dysregulated pathways identified in canine melanoma by integrated comparative genomic analysis

Winnie S. Liang, M. Neff, W. Tembe, 2017, bioRxiv.

Loss of the tumor suppressor SMARCA4 in small cell carcinoma of the ovary, hypercalcemic type (SCCOHT)

Winnie S. Liang, B. Monk, J. Trent, 2014, Rare diseases.

Somatic inactivating PTPRJ mutations and dysregulated pathways identified in canine malignant melanoma by integrated comparative genomic analysis

Winnie S. Liang, J. Trent, M. Neff, 2018, PLoS genetics.

Novel functional insights revealed by distinct protein-protein interactions of the residual SWI/SNF complex in SMARCA4-deficient small cell carcinoma of the ovary, hypercalcemic type

J. Trent, D. Huntsman, A. Hegde, 2019, bioRxiv.

Canine osteosarcoma genome sequencing identifies recurrent mutations in DMD and the histone methyltransferase gene SETD2

Winnie S. Liang, J. Trent, P. Houghton, 2019, Communications Biology.

Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4

Jason J. Corneveaux, J. Trent, H. Cunliffe, 2014, Nature Genetics.

Ponatinib Shows Potent Antitumor Activity in Small Cell Carcinoma of the Ovary Hypercalcemic Type (SCCOHT) through Multikinase Inhibition

Winnie S. Liang, J. Trent, D. Huntsman, 2018, Clinical Cancer Research.

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

Hugo Y. K. Lam, Winnie S. Liang, Daoud M. Meerzaman, 2021, Nature Biotechnology.

Analyzing the potato abiotic stress transcriptome using expressed sequence tags.

Jia Liu, C Robin Buell, Victoria Zismann, 2005, Genome.

Expressed Sequence Tags from loblolly pine embryos reveal similarities with angiosperm embryogenesis

J. Cairney, F. Thibaud-Nissen, V. Zismann, 2006, Plant Molecular Biology.

Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1

J. Gilbert, D. Stephan, V. Zismann, 2008, Neurology.

Refinement of 2q and 7p loci in a large multiplex NTD family.

J. Gilbert, D. Stephan, J. Connelly, 2008, Birth defects research. Part A, Clinical and molecular teratology.

Personalized treatment of Sézary syndrome by targeting a novel CTLA4:CD28 fusion

Winnie S. Liang, S. Kruglyak, J. Carpten, 2014, Molecular genetics & genomic medicine.

Anchoring of rice BAC clones to the rice genetic map in silico.

John Quackenbush, R. Wing, V. Zismann, 2000, Nucleic acids research.

Sequence, annotation, and analysis of synteny between rice chromosome 3 and diverged grass species.

Rod A Wing, Wei Zhu, Carol Soderlund, 2005, Genome research.

Mitochondrial genome sequences and molecular evolution of the Irish potato famine pathogen, Phytophthora infestans

V. Zismann, C. Buell, J. Ristaino, 2005, Current Genetics.

Ponatinib shows potent antitumor activity in small cell carcinoma of the ovary hypercalcemic type (SCCOHT) through multi-kinase inhibition

Winnie S. Liang, J. Trent, D. Huntsman, 2017, bioRxiv.

Identifying treatment options for BRAFV600 wild-type metastatic melanoma: A SU2C/MRA genomics-enabled clinical trial

Rebecca F. Halperin, Winnie S. Liang, N. Schork, 2021, PloS one.

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

Edward R. Dougherty, Marcel Brun, Jianping Hua, 2007, Bioinform..

Identification of Genetic Susceptibility Factors Associated with Canine Gastric Dilatation-Volvulus

V. Zismann, I. Piras, W. Hendricks, 2020, Genes.

Identification of Recurrent Activating HER2 Mutations in Primary Canine Pulmonary Adenocarcinoma

Winnie S. Liang, J. Trent, D. Carbone, 2019, Clinical Cancer Research.

A CRISPR-enhanced metagenomic NGS test to improve pandemic preparedness

N. Schork, Y. Hakak, Yongwook Choi, 2023, Cell Reports Methods.

Canine osteosarcoma genome sequencing identifies recurrent mutations in DMD and the histone methyltransferase gene SETD2

Winnie S. Liang, J. Trent, P. Houghton, 2019, Communications Biology.

Identification of frequent activating HER2 mutations in primary canine pulmonary adenocarcinoma

Winnie S. Liang, J. Trent, D. Carbone, 2019, bioRxiv.

Sorl1 as an Alzheimer’s Disease Predisposition Gene?

Rebecca F. Halperin, D. Stephan, A. Myers, 2007, Neurodegenerative Diseases.

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

K. Brown, J. Trent, D. Bishop, 2011, Nature.

PUBLISHED VERSION

J. Trent, D. Bishop, D. Duffy, 2018 .

Identification of Genetic Susceptibility Factors Associated with Canine Gastric Dilatation-Volvulus

V. Zismann, I. Piras, N. Briones, 2020, Genes.

Pilot clinical trial and phenotypic analysis in chemotherapy-pretreated, metastatic triple-negative breast cancer patients treated with oral TAK-228 and TAK-117 (PIKTOR) to increase DNA damage repair deficiency followed by cisplatin and nab paclitaxel

V. Zismann, V. Espina, J. O’Shaughnessy, 2023, Biomarker Research.

Landscape of super-enhancers in small cell carcinoma of the ovary, hypercalcemic type and efficacy of targeting with natural product triptolide

D. Huntsman, V. Zismann, A. Karnezis, 2023, bioRxiv.

Evidence for an association between KIBRA and late-onset Alzheimer's disease

Jason J. Corneveaux, Winnie S. Liang, G. Alexander, 2010, Neurobiology of Aging.

SNiPer 500K: A Novel SNP Genotype Calling Algorithm

E. Dougherty, D. Stephan, D. Craig, 2006, 2006 IEEE/NLM Life Science Systems and Applications Workshop.

Identification of disease causing loci using an array-based genotyping approach on pooled DNA

E. Puffenberger, M. Huentelman, V. Zismann, 2005, BMC Genomics.

Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1

D. Stephan, V. Zismann, J. Stajich, 2008, Neurology.

Genomic analysis across 53 canine cancer types reveals novel mutations and high clinical actionability potential.

S. Byron, V. Zismann, Sharadha Sakthikumar, 2023, Veterinary and comparative oncology.

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

M. Huentelman, J. Webster, V. Zismann, 2007, Bioinform..

Genetics and population analysis SNiPer-HD : improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

E. Dougherty, D. Stephan, D. Craig, 2006 .

Sniper-hd: Improved Genotype Calling Accuracy by an Expecta- Tion-maximization Algorithm for High-density Snp Arrays

M. Huentelman, J. Webster, V. Zismann, 2022 .

The sequence of rice chromosomes 11 and 12 rich in disease resistance genes and recent gene duplicationsRice Chromosomes 11 and 12 Sequencing Consortia (RCSC)BMC Biol2005320126116516188032

S. Salzberg, O. White, J. Weissenbach, 2005 .