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Martin R. Pollak | Researchclopedia

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Martin R. Pollak

Beth Israel Deaconess Medical Center ORCID

294

Works

23,217

Citations

73

h-index

184

i10-index

Research Topics

Renal Diseases and Glomerulopathies Chronic Kidney Disease and Diabetes Renal and related cancers

Affiliations

Broad Institute2010–2024

University of Notre Dame1984–1984

Boston University2005–2005

Tougaloo College2013–2013

Brigham and Women's Hospital1993–2015

Top Works

Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans

Giulio Genovese,David J. Friedman,et al.

20102,008 citations

Parathyroid Disorders and Treatments

Chronic Lymphocytic Leukemia Research

Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

Joshua M. Kaplan,Sung Hyun Kim,et al.

20001,242 citations

Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Martin R. Pollak,Edward M. Brown,et al.

19931,049 citations

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

Jochen Reiser,Krishna R. Polu,et al.

2005847 citations

APOL1 Genetic Variants in Focal Segmental Glomerulosclerosis and HIV-Associated Nephropathy

Jeffrey B. Kopp,George W. Nelson,et al.

2011845 citations

Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor

Gregor B. Adams,Karissa T. Chabner,et al.

2005765 citations

Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation

Martin R. Pollak,Edward M. Brown,et al.

1994596 citations

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

Chrystal Ho,David A. Conner,et al.

1995592 citations

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

Elizabeth Brown,Johannes Schlöndorff,et al.

2009441 citations