Martin R. Pollak

Also affiliated with Beth Israel Deaconess Medical Center, Harvard University

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 27 papers. Top paper: “Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference”.

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Kidney International(2022)10.1016/j.kint.2022.03.019

N/A

4.5DataRank · unranked

193 citations

Émilie Cornec-Le Gall, Jan Halbritter, Krzysztof Kiryluk, Andrew Mallett, Rulan S. Parekh +57 more

Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals

JAMA Network Open(2022)10.1001/jamanetworkopen.2022.1048

N/A

1.4DataRank · unranked

26 citations

Kezhen Fei, Michelle A. Ramos, Diane Hauser, Emilia Bagiella, Stephen B. Ellis +10 more

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Nature Genetics(2013)10.1038/ng.2543

N/A

0.862DataRank · unranked

313 citations

Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel +43 more

Nephrotic Syndrome Gene TBC1D8B Is Required for Endosomal Maturation and Nephrin Endocytosis in Drosophila

Journal of the American Society of Nephrology(2022)10.1681/asn.2022030275

N/A

0.854DataRank · unranked

26 citations

Camille Lempicki, Konrad Lang, Helena Heinkele, Lina L. Kampf, Claire Leroy +11 more

Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy

Journal of the American Society of Nephrology(2024)10.1681/asn.0000000501

N/A

0.709DataRank · unranked

16 citations

Andrew Beenken, Elena Martinelli, Ken Saida, Andrea L. Knob, Juntao Ke +45 more

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

Nature Communications(2023)10.1038/s41467-023-43020-9

N/A

0.637DataRank · unranked

69 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk Variants

Journal of the American Society of Nephrology(2022)10.1681/asn.2021050723

N/A

0.553DataRank · unranked

39 citations

Cristian V. Riella, Hyunjae Chung, Shrijal S. Shah, Minxian Wang, Jose M. Magraner +7 more

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.008

N/A

0.489DataRank · unranked

25 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

medRxiv(2023)10.1101/2023.08.02.23293554

N/A

0.208DataRank · unranked

3 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

Apolipoprotein L1 Opinions of African American Living Kidney Donors, Kidney Transplant Patients, and Nonpatients

Journal of Surgical Research(2022)10.1016/j.jss.2022.04.011

N/A

0DataRank · unranked

4 citations

Aaron Fleishman, Martha Pavlakis, Martin R. Pollak, Prabhakar K. Baliga, Vinayak Rohan +3 more

Disease Modeling with Kidney Organoids

Micromachines(2022)10.3390/mi13091384

N/A

0DataRank · unranked

10 citations

Martin R. Pollak, Balajikarthick Subramanian, Sophie Karp

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Nature Communications(2023)10.1038/s41467-023-37985-w

N/A

0DataRank · unranked

50 citations

Michelle T. McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Dêbiec, Yang Luo +65 more

APOL1 and APOL1-Associated Kidney Disease: A Common Disease, an Unusual Disease Gene – Proceedings of the Henry Shavelle Professorship

Glomerular Diseases(2023)10.1159/000529227

N/A

0DataRank · unranked

39 citations

David J. Friedman, Martin R. Pollak

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

medRxiv(2023)10.1101/2023.10.05.23296595

N/A

0DataRank · unranked

1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

APOL1 Bi- and Monoallelic Variants and Chronic Kidney Disease in West Africans

New England Journal of Medicine(2024)10.1056/nejmoa2404211

N/A

0DataRank · unranked

75 citations

Ifeoma Ulasi, Samuel Ajayi, Yemi Raheem Raji, Timothy O. Olanrewaju, Charlotte Osafo +44 more

APOL1 genotyping is incomplete without testing for the protective M1 modifier p.N264K variant

Glomerular Diseases(2024)10.1159/000537948

N/A

0DataRank · unranked

15 citations

Elena Martinelli, Yask Gupta, David J. Friedman, Matthew G. Sampson, Martin R. Pollak +2 more

Differing sensitivities to angiotensin converting enzyme inhibition of kidney disease mediated by APOL1 high-risk variants G1 and G2

Kidney International(2024)10.1016/j.kint.2024.07.026

N/A

0DataRank · unranked

10 citations

Sonako Jacas, Olivia Donovan, Diana Pintye, Nicholas Wiley, Zsuzsanna K. Zsengellér +5 more

The APOL1 p.N264K variant is co-inherited with the G2 kidney disease risk variant through a proximity recombination event

G3 Genes Genomes Genetics(2024)10.1093/g3journal/jkae290

N/A

0DataRank · unranked

8 citations

Michelle T. McNulty, Yask Gupta, Giulio Genovese, Matthew G. Sampson, Simone Sanna‐Cherchi +3 more

Nephrotic syndrome genomic discovery in the Mass General Brigham Biobank identifies monoallelic MEFV variants as a risk factor for focal segmental glomerulosclerosis

Kidney International(2025)10.1016/j.kint.2025.12.013

N/A

0DataRank · unranked

0 citations

Kristen M. Gibson, Juntao Ke, Zachary T. Sentell, Juliana E Arcila Galvis, Satoshi Koyama +23 more

FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes

Journal of the American Society of Nephrology(2020)10.1681/asn.2019050443

N/A

0DataRank · unranked

28 citations

Justin Chun, Chandra Perez-Gill, Paul Yan, Isaac E. Stillman, Henry N. Higgs +4 more

Dysregulated Dynein-Mediated Trafficking of Nephrin Causes INF2-related Podocytopathy

Journal of the American Society of Nephrology(2020)10.1681/asn.2020081109

N/A

0DataRank · unranked

29 citations

Chandra Perez-Gill, Johannes Schlöndorff, Balajikarthick Subramanian, Martin R. Pollak, Hua Sun

Autosomal Dominant Tubulointerstitial Kidney Disease—Uromodulin Misclassified as Focal Segmental Glomerulosclerosis or Hereditary Glomerular Disease

Kidney International Reports(2020)10.1016/j.ekir.2019.12.016

N/A

0DataRank · unranked

26 citations

Minxian Wang, Maris S. Wilkins, Andrea U. Knob, Ava Benjamin, Lihong Bu +2 more

Recessive, gain-of-function toxicity in an APOL1 BAC transgenic mouse model mirrors human APOL1 kidney disease

Disease Models & Mechanisms(2021)10.1242/dmm.048952

N/A

0DataRank · unranked

64 citations

Angelo Blasio, Olivia G Donovan, Lena B. Schaller, Althea Bock-Hughes, Jose M. Magraner +9 more

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.008

N/A

0DataRank · unranked

27 citations

Amar J. Majmundar, Kamal Khan, Tze Yin Lim, Shirlee Shril, Gina Jin +62 more

A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis

Kidney International(2021)10.1016/j.kint.2021.10.041

N/A

0DataRank · unranked

20 citations

Damian Fermin, Felix Eichinger, Dongkeun Jang, Matthias Kretzler, Noël P. Burtt +90 more

A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

Journal of the American Society of Nephrology(2021)10.1681/asn.2020081234

N/A

0DataRank · unranked

7 citations

Susan Murray, Katherine A. Benson, Agnieszka Bierżyńska, Megan Chryst-Stangl, Liming Wang +21 more

A glomerular transcriptomic landscape of APOL1 in Black patients with focal segmental glomerulosclerosis

medRxiv(2021)10.1101/2021.02.18.21251945

N/A

0DataRank · unranked

0 citations

Damian Fermin, Felix Eichinger, Dongkeun Jang, Matthias Kretzler, Noël P. Burtt +6 more