K. Deffenbacher

发表

Genome-wide miRNAprofiling of mantle cell lymphoma reveals a distinctsubgroup with poor prognosis

L. Staudt, A. Rosenwald, W. Chan, 2019 .

lymphoma and prognostication in angioimmunoblastic T-cell lymphoma Molecular signatures to improve diagnosis in peripheral T-cell

W. Chan, T. Greiner, D. Weisenburger, 2013 .

LYMPHOID NEOPLASIA Molecular signatures to improve diagnosis in peripheral T-cell lymphoma and prognostication in angioimmunoblastic T-cell lymphoma

W. Chan, T. Greiner, D. Weisenburger, 2010 .

Use of Mechanical Circulatory Support in Chronic Total Occlusion Percutaneous Coronary Intervention.

C. Schmidt, F. Jaffer, B. Rangan, 2022, The American journal of cardiology.

Genomewide search and genetic localization of a second gene associated with autosomal dominant branchio-oto-renal syndrome: clinical and genetic implications.

C. Cremers, W. Kimberling, Shrawan Kumar, 2000, American journal of human genetics.

Molecular signatures to improve diagnosis in peripheral T-cell lymphoma and prognostication in angioimmunoblastic T-cell lymphoma.

W. Chan, T. Greiner, D. Weisenburger, 2010, Blood.

Gene expression profiling in lymphoma diagnosis and management.

W. Chan, J. Iqbal, Zhongfeng Liu, 2009, Best practice & research. Clinical haematology.

Genome-wide copy-number analyses reveal genomic abnormalities involved in transformation of follicular lymphoma.

L. Staudt, A. Rosenwald, W. Chan, 2014, Blood.

Global microRNA expression profiling uncovers molecular markers for classification and prognosis in aggressive B-cell lymphoma.

L. Staudt, A. Rosenwald, W. Chan, 2015, Blood.

Molecular distinctions between pediatric and adult mature B-cell non-Hodgkin lymphomas identified through genomic profiling.

L. Staudt, A. Rosenwald, W. Chan, 2012, Blood.

Identification of Racial Inequities in Access to Specialized Inpatient Heart Failure Care at an Academic Medical Center.

Brian W. Powers, Justin P. Tuwatananurak, Lisa S. Rotenstein, 2019, Circulation. Heart failure.

Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing.

C. Cremers, W. Kimberling, Shrawan Kumar, 1997, Genetic testing.

Genome-wide miRNA profiling of mantle cell lymphoma reveals a distinct subgroup with poor prognosis.

L. Staudt, A. Rosenwald, W. Chan, 2012, Blood.

EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family

W. Kimberling, Shrawan Kumar, S. Usami, 1999, Journal of Human Genetics.

Expression and Promoter Methylation of P16INK4A During Estrogen-Induced Mammary Carcinogenesis in the ACI Rat

K. Deffenbacher, 2006 .

Reading and Dyslexias

Shelley D. Smith, A. Brower, K. Deffenbacher, 2006 .

Reading Disability and Chromosome 6p21.3

J. W. Askew, R. Olson, Shelley D. Smith, 2001, Journal of learning disabilities.

Recurrent Chromosomal Alterations in Molecularly Classified AIDS-Related Lymphomas: An Integrated Analysis of DNA Copy Number and Gene Expression

Kai Fu, Javeed Iqbal, Zhongfeng Liu, 2010, Journal of acquired immune deficiency syndromes.

Development of a Novel Score to Predict Urgent Mechanical Circulatory Support in Chronic Total Occlusion Percutaneous Coronary Intervention

F. Jaffer, B. Rangan, E. Brilakis, 2022, medRxiv.

Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses

B. Pennington, R. Olson, J. Defries, 2004, Human Genetics.