Ahmet A. Kurdoglu

发表

Comprehensive Genomic Analysis of Metastatic Mucinous Urethral Adenocarcinoma Guides Precision Oncology Treatment: Targetable EGFR Amplification Leading to Successful Treatment With Erlotinib

J. Cheville, J. Carpten, D. Craig, 2016, Clinical genitourinary cancer.

An integrated map of genetic variation from 1,092 human genomes

Kenny Q. Ye, Mauricio O. Carneiro, Francisco M. De La Vega, 2012, Nature.

Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides.

J. Carpten, Y. Asmann, D. Craig, 2012, Blood.

Alzheimer's disease is associated with altered expression of genes involved in immune response and mitochondrial processes in astrocytes

Ahmet Kurdoglu, Jessica Aldrich, Eric M. Reiman, 2015, Neurobiology of Aging.

Integrated Genomic Characterization Reveals Novel, Therapeutically Relevant Drug Targets in FGFR and EGFR Pathways in Sporadic Intrahepatic Cholangiocarcinoma

Eric W. Klee, Stephen D. Mastrian, Ahmet Kurdoglu, 2014, PLoS genetics.

Clinical Implementation of Integrated Genomic Profiling in Patients with Advanced Cancers

Winnie S. Liang, J. Carpten, D. Craig, 2016, Scientific Reports.

Whole genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution and clonal tides Short title: Sequencing Reveals Natural History of Myeloma

J. Carpten, Y. Asmann, D. Craig, 2016 .

In vitro-differentiated neural cell cultures progress towards donor-identical brain tissue.

Rebecca A. Reiman, S. Szelinger, D. Craig, 2013, Human molecular genetics.

Bar-coded, multiplexed sequencing of targeted DNA regions using the Illumina Genome Analyzer.

S. Szelinger, D. Craig, Ahmet A. Kurdoglu, 2011, Methods in molecular biology.

Genome and Transcriptome Sequencing in Prospective Metastatic Triple-Negative Breast Cancer Uncovers Therapeutic Vulnerabilities

Francisco M. De La Vega, Ahmet Kurdoglu, Spyro Mousses, 2012, Molecular Cancer Therapeutics.

Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing

Winnie S. Liang, J. Carpten, G. Hostetter, 2012, PloS one.

A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi Syndrome.

Jason J. Corneveaux, S. Szelinger, D. Craig, 2015, Investigative ophthalmology & visual science.

Paired Tumor and Normal Whole Genome Sequencing of Metastatic Olfactory Neuroblastoma

Winnie S. Liang, J. Carpten, G. Hostetter, 2012, PloS one.

Long insert whole genome sequencing for copy number variant and translocation detection

Winnie S. Liang, J. Carpten, D. Craig, 2013, Nucleic acids research.

Abstract 4493: Germline findings in targeted tumor sequencing using matched normal DNA

J. Carpten, J. Trent, D. Craig, 2016 .

Novel pathogenic variants and genes for myopathies identified by whole exome sequencing

Winnie S. Liang, J. Carpten, S. Coons, 2015, Molecular genetics & genomic medicine.

Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing

Jason J. Corneveaux, J. Trent, S. Szelinger, 2014, PloS one.

Niche adaptation and genome expansion in the chlorophyll d-producing cyanobacterium Acaryochloris marina

Lawrence E. Page, M. Mimuro, Yuichiro Shimada, 2008, Proceedings of the National Academy of Sciences.

A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome

Jason J. Corneveaux, S. Szelinger, D. Craig, 2015, PloS one.

Multiethnic PDX models predict a possible immune signature associated with TNBC of African ancestry

S. Merajver, J. Carpten, J. Trent, 2021, Breast Cancer Research and Treatment.

Extramedullary myeloma whole genome sequencing reveals novel mutations in Cereblon, proteasome subunit G2 and the glucocorticoid receptor in multi drug resistant disease

Winnie S. Liang, J. Carpten, D. Craig, 2013, British journal of haematology.

Interim Analysis of the Mmrf Commpass Trial: Identification of Novel Rearrangements Potentially Associated with Disease Initiation and Progression

J. Carpten, S. Jewell, D. Rohrer, 2014 .

Interim Analysis Of The Mmrf Commpass Trial, a Longitudinal Study In Multiple Myeloma Relating Clinical Outcomes To Genomic and Immunophenotypic Profiles

Winnie S. Liang, J. Carpten, S. Jewell, 2013 .

Metabolic flexibility revealed in the genome of the cyst-forming α-1 proteobacterium Rhodospirillum centenum

Paul Stothard, Jeffrey W Touchman, Yih-Kuang Lu, 2010, BMC Genomics.

The Genome of Heliobacterium modesticaldum, a Phototrophic Representative of the Firmicutes Containing the Simplest Photosynthetic Apparatus � †

Lawrence E. Page, M. Madigan, J. Touchman, 2022 .

Whole genome sequencing reveals potential targets for therapy in patients with refractory KRASmutated metastatic colorectal cancer

Nicole A. Lavender, J. Carpten, G. Hostetter, 2014, BMC Medical Genomics.

Simultaneous Characterization of Somatic Events and HPV-18 Integration in a Metastatic Cervical Carcinoma Patient Using DNA and RNA Sequencing

Winnie S. Liang, J. Carpten, B. Monk, 2014, International Journal of Gynecologic Cancer.

Genomic Basis of Multiple Myeloma Subtypes from the MMRF CoMMpass Study

Winnie S. Liang, J. Carpten, S. Jewell, 2021, medRxiv.

Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer

Nicole A. Lavender, Winnie S. Liang, J. Carpten, 2014, BMC Medical Genomics.

A Pilot Study Using Next-Generation Sequencing in Advanced Cancers: Feasibility and Challenges

Winnie S. Liang, J. Carpten, G. Hostetter, 2013, PloS one.

Interim Analysis of the MMRF CoMMpass Study: Comprehensive Characterization of Multiple Myeloma Patients at Diagnosis Reveals Distinct Molecular Subtypes and Clinical Outcomes

Winnie S. Liang, J. Carpten, J. Fay, 2015 .

The Genome of Heliobacterium modesticaldum, a Phototrophic Representative of the Firmicutes Containing the Simplest Photosynthetic Apparatus

Lawrence E. Page, M. Madigan, J. Touchman, 2008, Journal of bacteriology.

Extramedullary myeloma whole genome sequencing reveals novel mutations in Cereblon, proteasome subunit G2 and the glucocorticoid receptor in multi drug resistant disease

Winnie S. Liang, J. Carpten, D. Craig, 2013, British journal of haematology.