Honors for Dr. Virginia LiVolsi, Dr. Zubair Baloch, and fourth-year resident Dr. Sam Wei.
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The Department mourns the death of Dr. Nicholas Gonatas, Professor of Pathology and Laboratory Medicine, luminary neuropathologist, world-class researcher, founder of the Division of Neuropathology at Penn, and outstanding teacher and mentor to scores of pathology fellows, residents, graduate students, and postdoctoral fellows.
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In a study that sheds light on how phospholipid signals are controlled during tumorigenesis, the Chen Lab reports that TIPE3, a newly described oncogenic protein, is the transfer protein of phosphoinositide second messengers that promote cancer.
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Melanoma physicians and researchers from Penn Medicine and The Wistar Institute have been awarded a prestigious $12.1 million NCI SPORE grant.
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Penn's Pathology Residency Program was ranked #2 in the nation for residents with a research focus, either translational or basic, and #1 for residents interested in basic and clinical research and fellowships in Neuropathology or Transfusion Medicine. In addition, the program ranked in the top 5 for residents interested in academic careers and Hematopathology, Molecular Genetics, and Cytopathology.
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Construction of a first-of-its-kind Center for Advanced Cellular Therapeutics at Penn Medicine has begun.
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Rachel L. Sargent, MD, a graduate of the Residency Program, has joined the Department as Assistant Professor and Attending Physician in the Section of Hematopathology.
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Dr. David Weiner is among the 2014 Top 50 "Most Influential People in Vaccines." Dr. Weiner’s research in the area of Molecular Immunology has focused extensively on the development of gene-based vaccines and immune therapies.
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A drug developed by the Lambris Lab has received orphan status in Europe for the treatment of paroxysmal nocturnal hemoglobinuria (PNH), a rare, life-threatening disease that causes anemia due to destruction of red blood cells and thrombosis.
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The lab of James M. Wilson, MD, PhD, director of the Penn Gene Therapy Program, has published a proof-of-principle animal study that reduces harmful accumulation of proteins in a rare lysosomal storage disease through direct gene therapy.
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