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A major focus of both my clinical practice and investigative work is the diagnosis and treatment of disorders affecting solid-organ transplant recipients, particularly infectious complications. For the past 15 years, I have served as the primary pathologist for one of the largest lung transplant programs in the world; in the process contributing to over 20 peer-reviewed publications on complications of lung transplantation, including infections, gastroesophageal reflux, tumors, and antibody-mediated rejection; and writing a major book chapter on the subject (Howell DN and Palmer SM, Pathology of the Lung Transplant. 2006. In: Lynch JP, Ross D, eds. Lung and Heart-Lung Transplantation. Marcel Dekker, Inc., New York, pp. 683-722). I have also been the primary pathologist for Duke's renal and liver transplant programs, authoring or co-authoring a wide variety of journal articles and a book chapter in these areas (e.g., Plumb et al., Transplantation 2006;82:1224-1224; Snyder et al., Am. J. Respir. Crit. Care Med. 2010;181:1391-1396).
A second major area of interest is the pathogenesis of renal glomerular diseases. In collaboration with members of the Division of Nephrology at Duke, I have helped assemble and characterize a large registry of patients with familial focal segmental glomerulosclerosis (FFSGS)(Conlon et al., Kidney Int. 1999;56:1863-1871). Analysis of one of the families in this registry led to the discovery at Duke, in the laboratory of Dr. Michelle Winn, of mutations in the TRPC6 cation channel as a cause of FFSGS (Winn et al., Genomics 1999;58:113-120; Winn et al., Science 2005;308:1801-1804). We are continuing to collect data on additional families with focal segmental glomerulosclerosis. In addition, I have served as principle consultative pathologist for several investigators working in animal models of renal disease and transplantation (e.g., Crowley et al., Hypertension 2010;55:99-108).
A second major area of interest is the pathogenesis of renal glomerular diseases. In collaboration with members of the Division of Nephrology at Duke, I have helped assemble and characterize a large registry of patients with familial focal segmental glomerulosclerosis (FFSGS)(Conlon et al., Kidney Int. 1999;56:1863-1871). Analysis of one of the families in this registry led to the discovery at Duke, in the laboratory of Dr. Michelle Winn, of mutations in the TRPC6 cation channel as a cause of FFSGS (Winn et al., Genomics 1999;58:113-120; Winn et al., Science 2005;308:1801-1804). We are continuing to collect data on additional families with focal segmental glomerulosclerosis. In addition, I have served as principle consultative pathologist for several investigators working in animal models of renal disease and transplantation (e.g., Crowley et al., Hypertension 2010;55:99-108).
研究兴趣
论文共 17 篇作者统计合作学者相似作者
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Nader Abraham,Qimeng Gao,Riley Kahan,Isaac S. Alderete,Bangchen Wang,David N. Howell,Imran J. Anwar,Joseph M. Ladowski,Kentaro Nakata, Ethan Jarrett, Kendall Hlewicki,Greta Cywinska, Ryan Neill, Charles Aardema,David A. Gerber,Prabir Roy-Chaudhury, Benjamin A. Hughes,Matthew G. Hartwig,Andrew S. Barbas
Ultrastructural pathologypp.1-6, (2024)
Brandon M Lane,Susan Murray,Katherine Benson,Agnieszka Bierzynska,Megan Chryst-Stangl, Liming Wang,Guanghong Wu,Gianpiero Cavalleri,Brendan Doyle,Neil Fennelly,Anthony Dorman, Shane Conlon,Virginia Vega-Warner,Damian Fermin,Poornima Vijayan,Mohammad Azfar Qureshi,Shirlee Shril,Moumita Barua,Friedhelm Hildebrandt,Martin Pollak,David Howell,Matthew G Sampson,Moin Saleem,Peter J Conlon,Robert Spurney,Rasheed Gbadegesin
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGYno. 7 (2021): 1682-1695
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作者统计
#Papers: 17
#Citation: 104
H-Index: 4
G-Index: 4
Sociability: 5
Diversity: 3
Activity: 6
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