| Year |
Citation |
Score |
| 2020 |
Ngo D, Wen D, Gao Y, Keyes MJ, Drury ER, Katz DH, Benson MD, Sinha S, Shen D, Farrell LA, Peterson BD, Friedman DJ, Elmariah S, Young BA, Smith JG, ... ... Pollak MR, et al. Circulating testican-2 is a podocyte-derived marker of kidney health. Proceedings of the National Academy of Sciences of the United States of America. PMID 32958645 DOI: 10.1073/Pnas.2009606117 |
0.366 |
|
| 2020 |
Datta S, Kataria R, Zhang JY, Moore S, Petitpas K, Mohamed A, Zahler N, Pollak MR, Olabisi OA. Kidney Disease-Associated Variants Have Dose-Dependent, Dominant Toxic Gain-of-Function. Journal of the American Society of Nephrology : Jasn. PMID 32675303 DOI: 10.1681/Asn.2020010079 |
0.388 |
|
| 2020 |
Friedman DJ, Pollak MR. APOL1 Nephropathy: From Genetics to Clinical Applications. Clinical Journal of the American Society of Nephrology : Cjasn. PMID 32616495 DOI: 10.2215/Cjn.15161219 |
0.398 |
|
| 2020 |
Feng D, Kumar M, Muntel J, Gurley SB, Birrane G, Stillman IE, Ding L, Wang M, Ahmed S, Schlondorff J, Alper SL, Ferrante T, Marquez SL, Ng CF, Novak R, ... ... Pollak MR, et al. Phosphorylation of ACTN4 Leads to Podocyte Vulnerability and Proteinuric Glomerulosclerosis. Journal of the American Society of Nephrology : Jasn. PMID 32540856 DOI: 10.1681/Asn.2019101032 |
0.394 |
|
| 2020 |
Chun J, Wang M, Wilkins MS, Knob AU, Benjamin A, Bu L, Pollak MR. Autosomal Dominant Tubulointerstitial Kidney Disease-Uromodulin Misclassified as Focal Segmental Glomerulosclerosis or Hereditary Glomerular Disease. Kidney International Reports. 5: 519-529. PMID 32274456 DOI: 10.1016/J.Ekir.2019.12.016 |
0.421 |
|
| 2020 |
Pollak MR, Friedman DJ. The Genetic Architecture of Kidney Disease. Clinical Journal of the American Society of Nephrology : Cjasn. PMID 31992573 DOI: 10.2215/Cjn.09340819 |
0.421 |
|
| 2020 |
Subramanian B, Chun J, Perez-Gill C, Yan P, Stillman IE, Higgs HN, Alper SL, Schlöndorff JS, Pollak MR. FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes. Journal of the American Society of Nephrology : Jasn. PMID 31924668 DOI: 10.1681/Asn.2019050443 |
0.349 |
|
| 2019 |
Ware EB, Smith JA, Zhao W, Ganesvoort RT, Curhan GC, Pollak M, Mount DB, Turner ST, Chen G, Shah RJ, Kardia SLR, Lieske JC. Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid. Mayo Clinic Proceedings. Innovations, Quality & Outcomes. 3: 448-460. PMID 31993563 DOI: 10.1016/J.Mayocpiqo.2019.08.007 |
0.316 |
|
| 2019 |
Friedman DJ, Pollak MR. and Kidney Disease: From Genetics to Biology. Annual Review of Physiology. PMID 31710572 DOI: 10.1146/Annurev-Physiol-021119-034345 |
0.42 |
|
| 2019 |
Lannon H, Shah SS, Dias L, Blackler D, Alper SL, Pollak MR, Friedman DJ. Apolipoprotein L1 (APOL1) risk variant toxicity depends on the haplotype background. Kidney International. PMID 31611067 DOI: 10.1016/J.Kint.2019.07.010 |
0.349 |
|
| 2019 |
Drury ER, Friedman DJ, Pollak MR, Ix JH, Kuller LH, Tracy RP, Mukamal KJ. APOL1 gene variants and kidney disease in whites: the cardiovascular health study. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. PMID 31580460 DOI: 10.1093/Ndt/Gfz186 |
0.357 |
|
| 2019 |
Shah SS, Lannon H, Dias L, Zhang JY, Alper SL, Pollak MR, Friedman DJ. APOL1 Kidney Risk Variants Induce Cell Death Mitochondrial Translocation and Opening of the Mitochondrial Permeability Transition Pore. Journal of the American Society of Nephrology : Jasn. PMID 31558683 DOI: 10.1681/Asn.2019020114 |
0.359 |
|
| 2019 |
Drury ER, Stillman IE, Pollak MR, Denker BM. Autosomal Recessive Alport Syndrome Unveiled by Pregnancy. Nephron. 1-5. PMID 31408864 DOI: 10.1159/000502147 |
0.37 |
|
| 2019 |
Riella C, Siemens TA, Wang M, Campos RP, Moraes TP, Riella LV, Friedman DJ, Riella MC, Pollak MR. APOL1-Associated Kidney Disease in Brazil. Kidney International Reports. 4: 923-929. PMID 31317114 DOI: 10.1016/J.Ekir.2019.03.006 |
0.386 |
|
| 2019 |
Wang M, Chun J, Genovese G, Knob AU, Benjamin A, Wilkins MS, Friedman DJ, Appel GB, Lifton RP, Mane S, Pollak MR. Contributions of Rare Gene Variants to Familial and Sporadic FSGS. Journal of the American Society of Nephrology : Jasn. PMID 31308072 DOI: 10.1681/Asn.2019020152 |
0.338 |
|
| 2019 |
Chun J, Zhang JY, Wilkins MS, Subramanian B, Riella C, Magraner JM, Alper SL, Friedman DJ, Pollak MR. Recruitment of APOL1 kidney disease risk variants to lipid droplets attenuates cell toxicity. Proceedings of the National Academy of Sciences of the United States of America. PMID 30733285 DOI: 10.1073/Pnas.1820414116 |
0.345 |
|
| 2019 |
Poyan Mehr A, Sadeghi-Najafabadi M, Chau K, Messmer J, Pai R, Roy N, Friedman D, Pollak MR, Schlondorff J, Naljayan M, Singh T, Lecker SH, Rodby R, Germain M, Rennke H, et al. The Glomerular Disease Study and Trial Consortium: A Grassroots Initiative to Foster Collaboration and Innovation. Kidney International Reports. 4: 20-29. PMID 30596165 DOI: 10.1016/J.Ekir.2018.09.012 |
0.327 |
|
| 2018 |
Subramanian B, Kaya O, Pollak MR, Yao G, Zhou J. Guided tissue organization and disease modeling in a kidney tubule array. Biomaterials. 183: 295-305. PMID 30189357 DOI: 10.1016/J.Biomaterials.2018.07.059 |
0.351 |
|
| 2018 |
Franceschini N, Kopp JB, Barac A, Martin LW, Li Y, Qian H, Reiner AP, Pollak M, Wallace RB, Rosamond WD, Winkler CA. Association of APOL1 With Heart Failure With Preserved Ejection Fraction in Postmenopausal African American Women. Jama Cardiology. PMID 29971324 DOI: 10.1001/Jamacardio.2018.1827 |
0.319 |
|
| 2018 |
Fan Y, Liu W, Bi R, Densmore MJ, Sato T, Mannstadt M, Yuan Q, Zhou X, Olauson H, Larsson TE, Toka HR, Pollak MR, Brown EM, Lanske B. Interrelated role of Klotho and calcium-sensing receptor in parathyroid hormone synthesis and parathyroid hyperplasia. Proceedings of the National Academy of Sciences of the United States of America. PMID 29618612 DOI: 10.1073/Pnas.1717754115 |
0.335 |
|
| 2018 |
Zhang JY, Wang M, Tian L, Genovese G, Yan P, Wilson JG, Thadhani R, Mottl AK, Appel GB, Bick AG, Sampson MG, Alper SL, Friedman DJ, Pollak MR.
modifies-induced kidney disease risk. Proceedings of the National Academy of Sciences of the United States of America. PMID 29531077 DOI: 10.1073/Pnas.1716113115 |
0.399 |
|
| 2018 |
Feng D, Notbohm J, Benjamin A, He S, Wang M, Ang LH, Bantawa M, Bouzid M, Del Gado E, Krishnan R, Pollak MR. Disease-causing mutation in α-actinin-4 promotes podocyte detachment through maladaptation to periodic stretch. Proceedings of the National Academy of Sciences of the United States of America. PMID 29378953 DOI: 10.1073/Pnas.1717870115 |
0.336 |
|
| 2018 |
Feng D, DuMontier C, Pollak MR. The mechanical challenges and cytoskeletal impairments in focal segmental glomerulosclerosis. American Journal of Physiology. Renal Physiology. PMID 29363327 DOI: 10.1152/Ajprenal.00641.2017 |
0.33 |
|
| 2017 |
Pollak MR. Introduction: APOL1-Associated Kidney Disease. Seminars in Nephrology. 37: 489. PMID 29110755 DOI: 10.1016/J.Semnephrol.2017.07.001 |
0.373 |
|
| 2017 |
Wang H, Pun PH, Kwee L, Craig D, Haynes C, Chryst-Ladd M, Svetkey LP, Patel UD, Hauser ER, Pollak MR, Kraus WE, Shah SH. Apolipoprotein L1 Genetic Variants Are Associated with Chronic Kidney Disease but Not with Cardiovascular Disease in a Population Referred for Cardiac Catheterization. Cardiorenal Medicine. 7: 96-103. PMID 28611783 DOI: 10.1159/000453458 |
0.379 |
|
| 2017 |
Sato T, Courbebaisse M, Ide N, Fan Y, Hanai JI, Kaludjerovic J, Densmore MJ, Yuan Q, Toka HR, Pollak MR, Hou J, Lanske B. Parathyroid hormone controls paracellular Ca(2+) transport in the thick ascending limb by regulating the tight-junction protein Claudin14. Proceedings of the National Academy of Sciences of the United States of America. PMID 28373577 DOI: 10.1073/Pnas.1616733114 |
0.327 |
|
| 2017 |
Skorecki KL, Lee JH, Langefeld CD, Rosset S, Tzur S, Wasser WG, Shemer R, Hawkins GA, Divers J, Parekh RS, Li M, Sampson MG, Kretzler M, Pollak MR, Shah S, et al. A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. PMID 28339911 DOI: 10.1093/Ndt/Gfw451 |
0.343 |
|
| 2016 |
Greka A, Gibson D, Mundel P, Demetri G, Hildebrandt F, Pollak M, Florez J. Personalized Comments on Challenges and Opportunities in Kidney Disease Therapeutics: The Glom-NExT Symposium. Seminars in Nephrology. 36: 448. PMID 27987543 DOI: 10.1016/J.Semnephrol.2016.09.005 |
0.345 |
|
| 2016 |
Feng D, Steinke JM, Krishnan R, Birrane G, Pollak MR. Functional Validation of an Alpha-Actinin-4 Mutation as a Potential Cause of an Aggressive Presentation of Adolescent Focal Segmental Glomerulosclerosis: Implications for Genetic Testing. Plos One. 11: e0167467. PMID 27977723 DOI: 10.1371/Journal.Pone.0167467 |
0.427 |
|
| 2016 |
Olabisi O, Al-Romaih K, Henderson J, Tomar R, Drummond I, MacRae C, Pollak M. From man to fish: What can Zebrafish tell us about ApoL1 nephropathy? Clinical Nephrology. PMID 27509583 DOI: 10.5414/Cnp86S116 |
0.32 |
|
| 2016 |
Subramanian B, Sun H, Yan P, Charoonratana VT, Higgs HN, Wang F, Lai KV, Valenzuela DM, Brown EJ, Schlöndorff JS, Pollak MR. Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine-induced kidney injury. Kidney International. PMID 27350175 DOI: 10.1016/J.Kint.2016.04.020 |
0.382 |
|
| 2016 |
Bondzie PA, Chen HA, Cao MZ, Tomolonis JA, He F, Pollak MR, Henderson JM. Non-muscle Myosin-IIA is Critical for Podocyte F-actin Organization, Contractility and Attenuation of Cell Motility. Cytoskeleton (Hoboken, N.J.). PMID 27232264 DOI: 10.1002/Cm.21313 |
0.308 |
|
| 2016 |
Friedman DJ, Pollak MR. Apolipoprotein L1 and Kidney Disease in African Americans. Trends in Endocrinology and Metabolism: Tem. PMID 26947522 DOI: 10.1016/J.Tem.2016.02.002 |
0.411 |
|
| 2016 |
Sharma AK, Friedman DJ, Pollak MR, Alper SL. Structural characterization of the C-terminal coiled coil domains of wild-type and kidney disease associated mutants of Apolipoprotein L1. The Febs Journal. PMID 26945671 DOI: 10.1111/Febs.13706 |
0.32 |
|
| 2015 |
Olabisi OA, Zhang JY, VerPlank L, Zahler N, DiBartolo S, Heneghan JF, Schlöndorff JS, Suh JH, Yan P, Alper SL, Friedman DJ, Pollak MR. APOL1 kidney disease risk variants cause cytotoxicity by depleting cellular potassium and inducing stress-activated protein kinases. Proceedings of the National Academy of Sciences of the United States of America. PMID 26699492 DOI: 10.1073/Pnas.1522913113 |
0.331 |
|
| 2015 |
Mukamal KJ, Tremaglio J, Friedman DJ, Ix JH, Kuller LH, Tracy RP, Pollak MR. APOL1 Genotype, Kidney and Cardiovascular Disease, and Death in Older Adults. Arteriosclerosis, Thrombosis, and Vascular Biology. PMID 26634651 DOI: 10.1161/Atvbaha.115.305970 |
0.356 |
|
| 2015 |
MacRae CA, Pollak MR. Effect Size Does Matter: The Long Road to Mechanistic Insight From Genome Wide Association. Circulation. PMID 26487758 DOI: 10.1161/Circulationaha.115.019306 |
0.336 |
|
| 2015 |
Feng D, DuMontier C, Pollak MR. The role of alpha-actinin-4 in human kidney disease. Cell & Bioscience. 5: 44. PMID 26301083 DOI: 10.1186/S13578-015-0036-8 |
0.446 |
|
| 2015 |
Sampson MG, Pollak MR. Opportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic Era. Seminars in Nephrology. 35: 212-21. PMID 26215859 DOI: 10.1016/J.Semnephrol.2015.04.002 |
0.344 |
|
| 2015 |
Toka HR, Pollak MR, Houillier P. Calcium Sensing in the Renal Tubule. Physiology (Bethesda, Md.). 30: 317-26. PMID 26136545 DOI: 10.1152/Physiol.00042.2014 |
0.321 |
|
| 2015 |
Pollak MR. Modifiers of Cardiac Phenotypes. Circulation. Cardiovascular Genetics. 8: 425-6. PMID 26082553 DOI: 10.1161/Circgenetics.115.001122 |
0.358 |
|
| 2015 |
Ruchi R, Genovese G, Lee J, Charoonratana VT, Bernhardy AJ, Alper SL, Kopp JB, Thadhani R, Friedman DJ, Pollak MR. Copy Number Variation at the APOL1 Locus. Plos One. 10: e0125410. PMID 25933006 DOI: 10.1371/Journal.Pone.0125410 |
0.403 |
|
| 2015 |
Pollak MR. Idiopathic pediatric chronic kidney disease: can genomic technology crack the case? The Journal of Clinical Investigation. 125: 1799-800. PMID 25893596 DOI: 10.1172/Jci81509 |
0.307 |
|
| 2015 |
Kopp JB, Winkler CA, Zhao X, Radeva MK, Gassman JJ, D'Agati VD, Nast CC, Wei C, Reiser J, Guay-Woodford LM, Pollak MR, Hildebrandt F, Moxey-Mims M, Gipson DS, Trachtman H, et al. Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial. Journal of the American Society of Nephrology : Jasn. 26: 1443-8. PMID 25573908 DOI: 10.1681/Asn.2013111242 |
0.335 |
|
| 2015 |
Nichols B, Jog P, Lee JH, Blackler D, Wilmot M, D'Agati V, Markowitz G, Kopp JB, Alper SL, Pollak MR, Friedman DJ. Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1. Kidney International. 87: 332-42. PMID 25100047 DOI: 10.1038/Ki.2014.270 |
0.354 |
|
| 2015 |
Ma L, Shelness GS, Snipes JA, Murea M, Antinozzi PA, Cheng D, Saleem MA, Satchell SC, Banas B, Mathieson PW, Kretzler M, Hemal AK, Rudel LL, Petrovic S, Weckerle A, ... Pollak MR, et al. Localization of APOL1 protein and mRNA in the human kidney: nondiseased tissue, primary cells, and immortalized cell lines. Journal of the American Society of Nephrology : Jasn. 26: 339-48. PMID 25012173 DOI: 10.1681/Asn.2013091017 |
0.321 |
|
| 2014 |
Sun H, Al-Romaih KI, MacRae CA, Pollak MR. Human Kidney Disease-causing INF2 Mutations Perturb Rho/Dia Signaling in the Glomerulus. Ebiomedicine. 1: 107-15. PMID 26086034 DOI: 10.1016/J.Ebiom.2014.11.009 |
0.402 |
|
| 2014 |
Toka HR, Pollak MR. The role of the calcium-sensing receptor in disorders of abnormal calcium handling and cardiovascular disease. Current Opinion in Nephrology and Hypertension. 23: 494-501. PMID 24992569 DOI: 10.1097/Mnh.0000000000000042 |
0.309 |
|
| 2014 |
Grgic I, Hofmeister AF, Genovese G, Bernhardy AJ, Sun H, Maarouf OH, Bijol V, Pollak MR, Humphreys BD. Discovery of new glomerular disease-relevant genes by translational profiling of podocytes in vivo. Kidney International. 86: 1116-29. PMID 24940801 DOI: 10.1038/Ki.2014.204 |
0.326 |
|
| 2014 |
Thomson R, Genovese G, Canon C, Kovacsics D, Higgins MK, Carrington M, Winkler CA, Kopp J, Rotimi C, Adeyemo A, Doumatey A, Ayodo G, Alper SL, Pollak MR, Friedman DJ, et al. Evolution of the primate trypanolytic factor APOL1. Proceedings of the National Academy of Sciences of the United States of America. 111: E2130-9. PMID 24808134 DOI: 10.1073/Pnas.1400699111 |
0.375 |
|
| 2014 |
Gbadegesin RA, Hall G, Adeyemo A, Hanke N, Tossidou I, Burchette J, Wu G, Homstad A, Sparks MA, Gomez J, Jiang R, Alonso A, Lavin P, Conlon P, Korstanje R, ... ... Pollak MR, et al. Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS. Journal of the American Society of Nephrology : Jasn. 25: 1991-2002. PMID 24676636 DOI: 10.1681/Asn.2013090976 |
0.437 |
|
| 2014 |
Barua M, Stellacci E, Stella L, Weins A, Genovese G, Muto V, Caputo V, Toka HR, Charoonratana VT, Tartaglia M, Pollak MR. Mutations in PAX2 associate with adult-onset FSGS. Journal of the American Society of Nephrology : Jasn. 25: 1942-53. PMID 24676634 DOI: 10.1681/Asn.2013070686 |
0.405 |
|
| 2014 |
Brown EJ, Pollak MR, Barua M. Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing. Kidney International. 85: 1030-8. PMID 24599252 DOI: 10.1038/Ki.2014.48 |
0.311 |
|
| 2014 |
Ito K, Bick AG, Flannick J, Friedman DJ, Genovese G, Parfenov MG, Depalma SR, Gupta N, Gabriel SB, Taylor HA, Fox ER, Newton-Cheh C, Kathiresan S, Hirschhorn JN, Altshuler DM, ... Pollak MR, et al. Increased burden of cardiovascular disease in carriers of APOL1 genetic variants. Circulation Research. 114: 845-50. PMID 24379297 DOI: 10.1161/Circresaha.114.302347 |
0.351 |
|
| 2014 |
Bruggeman LA, O'Toole JF, Ross MD, Madhavan SM, Smurzynski M, Wu K, Bosch RJ, Gupta S, Pollak MR, Sedor JR, Kalayjian RC. Plasma apolipoprotein L1 levels do not correlate with CKD. Journal of the American Society of Nephrology : Jasn. 25: 634-44. PMID 24231663 DOI: 10.1681/Asn.2013070700 |
0.341 |
|
| 2014 |
Barua M, Shieh E, Schlondorff J, Genovese G, Kaplan BS, Pollak MR. Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis. Kidney International. 85: 124-33. PMID 24048372 DOI: 10.1038/Ki.2013.354 |
0.412 |
|
| 2013 |
Ashraf S, Gee HY, Woerner S, Xie LX, Vega-Warner V, Lovric S, Fang H, Song X, Cattran DC, Avila-Casado C, Paterson AD, Nitschké P, Bole-Feysot C, Cochat P, Esteve-Rudd J, ... ... Pollak M, et al. ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption. The Journal of Clinical Investigation. 123: 5179-89. PMID 24270420 DOI: 10.1172/Jci69000 |
0.368 |
|
| 2013 |
Williams WW, Pollak MR. Health disparities in kidney disease - Emerging data from the human genome New England Journal of Medicine. 369: 2260-2261. PMID 24206461 DOI: 10.1056/Nejme1312797 |
0.347 |
|
| 2013 |
Toka HR, Genovese G, Mount DB, Pollak MR, Curhan GC. Frequency of rare allelic variation in candidate genes among individuals with low and high urinary calcium excretion. Plos One. 8: e71885. PMID 23991001 DOI: 10.1371/Journal.Pone.0071885 |
0.334 |
|
| 2013 |
Toka HR, Yang J, Zera CA, Duffield JS, Pollak MR, Mount DB. Pregnancy-associated polyuria in familial renal glycosuria. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 62: 1160-4. PMID 23871407 DOI: 10.1053/J.Ajkd.2013.05.018 |
0.345 |
|
| 2013 |
Sun H, Schlondorff J, Higgs HN, Pollak MR. Inverted formin 2 regulates actin dynamics by antagonizing Rho/diaphanous-related formin signaling. Journal of the American Society of Nephrology : Jasn. 24: 917-29. PMID 23620398 DOI: 10.1681/Asn.2012080834 |
0.305 |
|
| 2013 |
Romero JR, Youte R, Brown EM, Pollak MR, Goltzman D, Karaplis A, Pong LC, Chien L, Chattopadhyay N, Rivera A. Parathyroid hormone ablation alters erythrocyte parameters that are rescued by calcium-sensing receptor gene deletion European Journal of Haematology. 91: 37-45. PMID 23528155 DOI: 10.1111/Ejh.12110 |
0.309 |
|
| 2013 |
Genovese G, Friedman DJ, Pollak MR. APOL1 variants and kidney disease in people of recent African ancestry. Nature Reviews. Nephrology. 9: 240-4. PMID 23438974 DOI: 10.1038/Nrneph.2013.34 |
0.428 |
|
| 2013 |
Kirby A, Gnirke A, Jaffe DB, Barešová V, Pochet N, Blumenstiel B, Ye C, Aird D, Stevens C, Robinson JT, Cabili MN, Gat-Viks I, Kelliher E, Daza R, DeFelice M, ... ... Pollak MR, et al. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Nature Genetics. 45: 299-303. PMID 23396133 DOI: 10.1038/Ng.2543 |
0.347 |
|
| 2013 |
Barua M, Brown EJ, Charoonratana VT, Genovese G, Sun H, Pollak MR. Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Kidney International. 83: 316-22. PMID 23014460 DOI: 10.1038/Ki.2012.349 |
0.399 |
|
| 2012 |
Toka HR, Al-Romaih K, Koshy JM, DiBartolo S, Kos CH, Quinn SJ, Curhan GC, Mount DB, Brown EM, Pollak MR. Deficiency of the calcium-sensing receptor in the kidney causes parathyroid hormone-independent hypocalciuria. Journal of the American Society of Nephrology : Jasn. 23: 1879-90. PMID 22997254 DOI: 10.1681/Asn.2012030323 |
0.354 |
|
| 2012 |
Lee BT, Kumar V, Williams TA, Abdi R, Bernhardy A, Dyer C, Conte S, Genovese G, Ross MD, Friedman DJ, Gaston R, Milford E, Pollak MR, Chandraker A. The APOL1 genotype of African American kidney transplant recipients does not impact 5-year allograft survival American Journal of Transplantation. 12: 1924-1928. PMID 22487534 DOI: 10.1111/J.1600-6143.2012.04033.X |
0.342 |
|
| 2012 |
Pollak MR, Genovese G, Friedman DJ. APOL1 and kidney disease. Current Opinion in Nephrology and Hypertension. 21: 179-82. PMID 22257798 DOI: 10.1097/Mnh.0B013E32835012Ab |
0.399 |
|
| 2012 |
Boucher I, Yu W, Beaudry S, Negoro H, Tran M, Pollak MR, Henderson JM, Denker BM. Gα12 activation in podocytes leads to cumulative changes in glomerular collagen expression, proteinuria and glomerulosclerosis. Laboratory Investigation; a Journal of Technical Methods and Pathology. 92: 662-75. PMID 22249312 DOI: 10.1038/Labinvest.2011.198 |
0.357 |
|
| 2011 |
Kanji Z, Powe CE, Wenger JB, Huang C, Ankers E, Sullivan DA, Collerone G, Powe NR, Tonelli M, Bhan I, Bernhardy AJ, Dibartolo S, Friedman D, Genovese G, Pollak MR, et al. Genetic variation in APOL1 associates with younger age at hemodialysis initiation. Journal of the American Society of Nephrology : Jasn. 22: 2091-7. PMID 21997398 DOI: 10.1681/Asn.2010121234 |
0.348 |
|
| 2011 |
Friedman DJ, Kozlitina J, Genovese G, Jog P, Pollak MR. Population-based risk assessment of APOL1 on renal disease. Journal of the American Society of Nephrology : Jasn. 22: 2098-105. PMID 21997396 DOI: 10.1681/Asn.2011050519 |
0.331 |
|
| 2011 |
Kopp JB, Nelson GW, Sampath K, Johnson RC, Genovese G, An P, Friedman D, Briggs W, Dart R, Korbet S, Mokrzycki MH, Kimmel PL, Limou S, Ahuja TS, Berns JS, ... ... Pollak M, et al. APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy. Journal of the American Society of Nephrology : Jasn. 22: 2129-37. PMID 21997394 DOI: 10.1681/Asn.2011040388 |
0.355 |
|
| 2011 |
Akilesh S, Suleiman H, Yu H, Stander MC, Lavin P, Gbadegesin R, Antignac C, Pollak M, Kopp JB, Winn MP, Shaw AS. Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis. The Journal of Clinical Investigation. 121: 4127-37. PMID 21911940 DOI: 10.1172/Jci46458 |
0.406 |
|
| 2011 |
Friedman DJ, Pollak MR. Genetics of kidney failure and the evolving story of APOL1 Journal of Clinical Investigation. 121: 3367-3374. PMID 21881214 DOI: 10.1172/Jci46263 |
0.415 |
|
| 2011 |
Shankland SJ, Pollak MR. A suPAR circulating factor causes kidney disease. Nature Medicine. 17: 926-7. PMID 21818086 DOI: 10.1038/Nm.2443 |
0.375 |
|
| 2011 |
Yao NY, Becker DJ, Broedersz CP, Depken M, Mackintosh FC, Pollak MR, Weitz DA. Nonlinear viscoelasticity of actin transiently cross-linked with mutant α-actinin-4. Journal of Molecular Biology. 411: 1062-71. PMID 21762701 DOI: 10.1016/J.Jmb.2011.06.049 |
0.314 |
|
| 2011 |
Al-Romaih KI, Genovese G, Al-Mojalli H, Al-Othman S, Al-Manea H, Al-Suleiman M, Al-Jondubi M, Atallah N, Al-Rodayyan M, Weins A, Pollak MR, Adra CN. Genetic diagnosis in consanguineous families with kidney disease by homozygosity mapping coupled with whole-exome sequencing. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 58: 186-95. PMID 21658830 DOI: 10.1053/J.Ajkd.2011.01.025 |
0.396 |
|
| 2011 |
Liakopoulos V, Huerta A, Cohen S, Pollak MR, Sirota RA, Superdock K, Appel GB. Familial collapsing focal segmental glomerulosclerosis Clinical Nephrology. 75: 362-368. PMID 21426891 DOI: 10.5414/Cn106544 |
0.32 |
|
| 2011 |
Sun H, Schlondorff JS, Brown EJ, Higgs HN, Pollak MR. Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2). Proceedings of the National Academy of Sciences of the United States of America. 108: 2933-8. PMID 21278336 DOI: 10.1073/Pnas.1017010108 |
0.381 |
|
| 2011 |
Wyss HM, Henderson JM, Byfield FJ, Bruggeman LA, Ding Y, Huang C, Suh JH, Franke T, Mele E, Pollak MR, Miner JH, Janmey PA, Weitz DA, Miller RT. Biophysical properties of normal and diseased renal glomeruli. American Journal of Physiology. Cell Physiology. 300: C397-405. PMID 21123730 DOI: 10.1152/Ajpcell.00438.2010 |
0.383 |
|
| 2011 |
Pollak M. Biological Mechanisms of Focal Glomerulosclerosis: A Major Cause of Acquired and Inherited Renal Disease Annual Review of Medicine. 63: 110301100719093. DOI: 10.1146/Annurev.Med.041608.121355 |
0.382 |
|
| 2010 |
Pollak MR. Genetics and genetic testing in kidney disease: introduction. Seminars in Nephrology. 30: 355. PMID 20807607 DOI: 10.1016/J.Semnephrol.2010.06.001 |
0.357 |
|
| 2010 |
Freedman BI, Kopp JB, Langefeld CD, Genovese G, Friedman DJ, Nelson GW, Winkler CA, Bowden DW, Pollak MR. The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans. Journal of the American Society of Nephrology : Jasn. 21: 1422-6. PMID 20688934 DOI: 10.1681/Asn.2010070730 |
0.377 |
|
| 2010 |
Genovese G, Tonna SJ, Knob AU, Appel GB, Katz A, Bernhardy AJ, Needham AW, Lazarus R, Pollak MR. A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. Kidney International. 78: 698-704. PMID 20668430 DOI: 10.1038/Ki.2010.251 |
0.385 |
|
| 2010 |
Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, ... ... Pollak MR, et al. Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science (New York, N.Y.). 329: 841-5. PMID 20647424 DOI: 10.1126/Science.1193032 |
0.375 |
|
| 2010 |
Grünfeld JP, Hwu W, Chien Y, Lee N, Chiang S, Dobrovolny R, Huang A, Yeh H, Chao M, Lin S, Kitagawa T, Desnick R, Hsu L, Van Keimpema L, Nevens F, ... ... Pollak M, et al. More on clinical renal genetics. Clinical Journal of the American Society of Nephrology : Cjasn. 5: 563-7. PMID 20338964 DOI: 10.2215/Cjn.01720210 |
0.371 |
|
| 2010 |
Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Tonna SJ, Uscinski AL, Higgs HN, Henderson JM, Pollak MR. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis. Nature Genetics. 42: 72-6. PMID 20023659 DOI: 10.1038/Ng.505 |
0.393 |
|
| 2009 |
Pollak MR. Expanding the spectrum of NPHS1-associated disease. Kidney International. 76: 1221-3. PMID 19946311 DOI: 10.1038/Ki.2009.391 |
0.363 |
|
| 2009 |
Pollak MR. Surprising results following conditional podocyte inactivation. Journal of the American Society of Nephrology : Jasn. 20: 2086-8. PMID 19762489 DOI: 10.1681/Asn.2009080854 |
0.357 |
|
| 2009 |
Egbuna O, Quinn S, Kantham L, Butters R, Pang J, Pollak M, Goltzman D, Brown E. The full-length calcium-sensing receptor dampens the calcemic response to 1alpha,25(OH)2 vitamin D3 in vivo independently of parathyroid hormone. American Journal of Physiology. Renal Physiology. 297: F720-8. PMID 19474191 DOI: 10.1152/Ajprenal.00164.2009 |
0.307 |
|
| 2009 |
Henderson JM, Alexander MP, Pollak MR. Patients with ACTN4 mutations demonstrate distinctive features of glomerular injury. Journal of the American Society of Nephrology : Jasn. 20: 961-8. PMID 19357256 DOI: 10.1681/Asn.2008060613 |
0.386 |
|
| 2009 |
Schlöndorff J, Del Camino D, Carrasquillo R, Lacey V, Pollak MR. TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription. American Journal of Physiology. Cell Physiology. 296: C558-69. PMID 19129465 DOI: 10.1152/Ajpcell.00077.2008 |
0.325 |
|
| 2008 |
Tonna SJ, Needham A, Polu K, Uscinski A, Appel GB, Falk RJ, Katz A, Al-Waheeb S, Kaplan BS, Jerums G, Savige J, Harmon J, Zhang K, Curhan GC, Pollak MR. NPHS2 variation in focal and segmental glomerulosclerosis. Bmc Nephrology. 9: 13. PMID 18823551 DOI: 10.1186/1471-2369-9-13 |
0.332 |
|
| 2008 |
Pollak MR. Kidney disease and African ancestry. Nature Genetics. 40: 1145-6. PMID 18818713 DOI: 10.1038/Ng1008-1145 |
0.369 |
|
| 2008 |
Ward SM, Weins A, Pollak MR, Weitz DA. Dynamic viscoelasticity of actin cross-linked with wild-type and disease-causing mutant alpha-actinin-4. Biophysical Journal. 95: 4915-23. PMID 18689451 DOI: 10.1529/Biophysj.108.131722 |
0.317 |
|
| 2008 |
Leibon G, Rockmore DN, Pollak MR. A SNP streak model for the identification of genetic regions identical-by-descent. Statistical Applications in Genetics and Molecular Biology. 7: Article16. PMID 18518857 DOI: 10.2202/1544-6115.1340 |
0.321 |
|
| 2008 |
Tong Z, Yang Z, Patel S, Chen H, Gibbs D, Yang X, Hau VS, Kaminoh Y, Harmon J, Pearson E, Buehler J, Chen Y, Yu B, Tinkham NH, Zabriskie NA, ... ... Pollak MR, et al. Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications. Proceedings of the National Academy of Sciences of the United States of America. 105: 6998-7003. PMID 18458324 DOI: 10.1073/Pnas.0800454105 |
0.326 |
|
| 2008 |
Pollak MR. Focal segmental glomerulosclerosis: recent advances. Current Opinion in Nephrology and Hypertension. 17: 138-42. PMID 18277145 DOI: 10.1097/Mnh.0B013E3282F5Dbe4 |
0.315 |
|
| 2008 |
Tonna S, Dandapani SV, Uscinski A, Appel GB, Schlöndorff JS, Zhang K, Denker BM, Pollak MR. Functional genetic variation in aminopeptidase A (ENPEP): lack of clear association with focal and segmental glomerulosclerosis (FSGS). Gene. 410: 44-52. PMID 18206321 DOI: 10.1016/J.Gene.2007.11.014 |
0.72 |
|
| 2008 |
Henderson JM, Al-Waheeb S, Weins A, Dandapani SV, Pollak MR. Mice with altered alpha-actinin-4 expression have distinct morphologic patterns of glomerular disease. Kidney International. 73: 741-50. PMID 18185509 DOI: 10.1038/Sj.Ki.5002751 |
0.696 |
|
| 2007 |
Mistry K, Ireland JH, Ng RC, Henderson JM, Pollak MR. Novel mutations in NPHP4 in a consanguineous family with histological findings of focal segmental glomerulosclerosis. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 50: 855-64. PMID 17954299 DOI: 10.1053/J.Ajkd.2007.08.009 |
0.431 |
|
| 2007 |
Pollak MR, Alexander MP, Henderson JM. A case of familial kidney disease. Clinical Journal of the American Society of Nephrology : Cjasn. 2: 1367-74. PMID 17942774 DOI: 10.2215/Cjn.02040507 |
0.356 |
|
| 2007 |
Weins A, Schlondorff JS, Nakamura F, Denker BM, Hartwig JH, Stossel TP, Pollak MR. Disease-associated mutant alpha-actinin-4 reveals a mechanism for regulating its F-actin-binding affinity. Proceedings of the National Academy of Sciences of the United States of America. 104: 16080-5. PMID 17901210 DOI: 10.1073/Pnas.0702451104 |
0.31 |
|
| 2007 |
Copelovitch L, Guttenberg M, Pollak MR, Kaplan BS. Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS. Pediatric Nephrology (Berlin, Germany). 22: 1779-84. PMID 17530296 DOI: 10.1007/S00467-007-0505-3 |
0.385 |
|
| 2007 |
Dandapani SV, Sugimoto H, Matthews BD, Kolb RJ, Sinha S, Gerszten RE, Zhou J, Ingber DE, Kalluri R, Pollak MR. Alpha-actinin-4 is required for normal podocyte adhesion. The Journal of Biological Chemistry. 282: 467-77. PMID 17082197 DOI: 10.1074/Jbc.M605024200 |
0.674 |
|
| 2006 |
Schlöndorff JS, Pollak MR. TRPC6 in glomerular health and disease: what we know and what we believe. Seminars in Cell & Developmental Biology. 17: 667-74. PMID 17116414 DOI: 10.1016/J.Semcdb.2006.11.003 |
0.415 |
|
| 2006 |
Dandapani SV, Pollak MR. The glomerular filter: Biologic and genetic complexity. Kidney International. 70: 980-2. PMID 16957744 DOI: 10.1038/Sj.Ki.5001801 |
0.701 |
|
| 2006 |
Möller CC, Pollak MR, Reiser J. The genetic basis of human glomerular disease. Advances in Chronic Kidney Disease. 13: 166-73. PMID 16580618 DOI: 10.1053/J.Ackd.2006.01.009 |
0.417 |
|
| 2005 |
Weins A, Kenlan P, Herbert S, Le TC, Villegas I, Kaplan BS, Appel GB, Pollak MR. Mutational and Biological Analysis of alpha-actinin-4 in focal segmental glomerulosclerosis. Journal of the American Society of Nephrology : Jasn. 16: 3694-701. PMID 16251236 DOI: 10.1681/Asn.2005070706 |
0.404 |
|
| 2005 |
Reiser J, Polu KR, Möller CC, Kenlan P, Altintas MM, Wei C, Faul C, Herbert S, Villegas I, Avila-Casado C, McGee M, Sugimoto H, Brown D, Kalluri R, Mundel P, ... ... Pollak MR, et al. TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function. Nature Genetics. 37: 739-44. PMID 15924139 DOI: 10.1038/Ng1592 |
0.41 |
|
| 2004 |
Ellinor PT, Moore RK, Patton KK, Ruskin JN, Pollak MR, Macrae CA. Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation. Heart (British Cardiac Society). 90: 1487-8. PMID 15547041 DOI: 10.1136/Hrt.2003.027227 |
0.351 |
|
| 2004 |
Yao J, Le TC, Kos CH, Henderson JM, Allen PG, Denker BM, Pollak MR. Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein. Plos Biology. 2: e167. PMID 15208719 DOI: 10.1371/Journal.Pbio.0020167 |
0.402 |
|
| 2004 |
Pereira AC, Pereira AB, Mota GF, Cunha RS, Herkenhoff FL, Pollak MR, Mill JG, Krieger JE. NPHS2 R229Q functional variant is associated with microalbuminuria in the general population. Kidney International. 65: 1026-30. PMID 14871423 DOI: 10.1111/J.1523-1755.2004.00479.X |
0.389 |
|
| 2003 |
Kos CH, Le TC, Sinha S, Henderson JM, Kim SH, Sugimoto H, Kalluri R, Gerszten RE, Pollak MR. Mice deficient in alpha-actinin-4 have severe glomerular disease. The Journal of Clinical Investigation. 111: 1683-90. PMID 12782671 DOI: 10.1172/Jci17988 |
0.35 |
|
| 2003 |
Pollak MR. The genetic basis of FSGS and steroid-resistant nephrosis. Seminars in Nephrology. 23: 141-6. PMID 12704574 DOI: 10.1053/Snep.2003.50014 |
0.402 |
|
| 2003 |
Kos CH, Karaplis AC, Peng JB, Hediger MA, Goltzman D, Mohammad KS, Guise TA, Pollak MR. The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormone. The Journal of Clinical Investigation. 111: 1021-8. PMID 12671051 DOI: 10.1172/Jci17416 |
0.357 |
|
| 2002 |
Tsukaguchi H, Sudhakar A, Le TC, Nguyen T, Yao J, Schwimmer JA, Schachter AD, Poch E, Abreu PF, Appel GB, Pereira AB, Kalluri R, Pollak MR. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele. The Journal of Clinical Investigation. 110: 1659-66. PMID 12464671 DOI: 10.1172/Jci16242 |
0.379 |
|
| 2002 |
Pollak MR. Inherited podocytopathies: FSGS and nephrotic syndrome from a genetic viewpoint. Journal of the American Society of Nephrology : Jasn. 13: 3016-23. PMID 12444222 DOI: 10.1097/01.Asn.0000039569.34360.5E |
0.368 |
|
| 2001 |
Kaplan J, Pollak MR. Familial focal segmental glomerulosclerosis Current Opinion in Nephrology and Hypertension. 10: 183-187. PMID 11224692 DOI: 10.1097/00041552-200103000-00005 |
0.332 |
|
| 2000 |
Kaplan JM, Kim SH, North KN, Rennke H, Correia LA, Tong HQ, Mathis BJ, RodrÃguez-Pérez JC, Allen PG, Beggs AH, Pollak MR. Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis. Nature Genetics. 24: 251-6. PMID 10700177 DOI: 10.1038/73456 |
0.431 |
|
| 1998 |
Brown EM, Pollak M, Hebert SC. The extracellular calcium-sensing receptor: Its role in health and disease Annual Review of Medicine. 49: 15-29. PMID 9509247 DOI: 10.1146/Annurev.Med.49.1.15 |
0.349 |
|
| 1998 |
Mathis BJ, Kim SH, Calabrese K, Haas M, Seidman JG, Seidman CE, Pollak MR. A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13: Rapid communication Kidney International. 53: 282-286. PMID 9461087 DOI: 10.1046/J.1523-1755.1998.00828.X |
0.326 |
|
| 1996 |
Pollak MR, Seidman CE, Brown EM. Three inherited disorders of calcium sensing Medicine. 75: 115-123. PMID 8965680 DOI: 10.1097/00005792-199605000-00001 |
0.361 |
|
| 1996 |
Károlyi L, Ziegler A, Pollak M, Fischbach M, Grzeschik K, Koch MC, Seyberth HW. Gitelman’s syndrome is genetically distinct from other forms of Bartter’s syndrome Pediatric Nephrology. 10: 551-554. PMID 8897553 DOI: 10.1007/S004670050158 |
0.312 |
|
| 1996 |
Bai M, Quinn S, Trivedi S, Kifor O, Pearce SHS, Pollak MR, Krapcho K, Hebert SC, Brown EM. Expression and characterization of inactivating and activating mutations in the human Ca2+(o)-sensing receptor Journal of Biological Chemistry. 271: 19537-19545. PMID 8702647 DOI: 10.1074/Jbc.271.32.19537 |
0.346 |
|
| 1995 |
Brown EM, Pollak M, Chou YH, Seidman CE, Seidman JG, Hebert SC. Cloning and functional characterization of extracellular Ca2+-sensing receptors from parathyroid and kidney Bone. 17. PMID 8579901 DOI: 10.1016/8756-3282(95)00199-N |
0.315 |
|
| 1995 |
Brown EM, Pollak M, Hebert SC. Sensing of extracellular Ca2+ by parathyroid and kidney cells: Cloning and characterization of an extracellular Ca2+-sensing receptor American Journal of Kidney Diseases. 25: 506-513. PMID 7872334 DOI: 10.1016/0272-6386(95)90118-3 |
0.323 |
|
| 1995 |
Brown EM, Pollak M, Hebert SC. Molecular mechanisms underlying the sensing of extracellular Ca2+ by parathyroid and kidney cells European Journal of Endocrinology. 132: 523-531. PMID 7749489 DOI: 10.1530/Eje.0.1320523 |
0.325 |
|
| 1995 |
Brown EM, Pollak M, Chou YHW, Seidman CE, Seidman JG, Hebert SC. The cloning of extracellular Ca2+-sensing receptors from parathyroid and kidney: Molecular mechanisms of extracellular Ca2+-sensing Journal of Nutrition. 125. PMID 7602378 DOI: 10.1093/Jn/125.Suppl_7.1965S |
0.304 |
|
| 1995 |
Hosokawa Y, Pollak MR, Brown EM, Arnold A. Mutational analysis of the extracellular Ca2+-sensing receptor gene in human parathyroid tumors Journal of Clinical Endocrinology and Metabolism. 80: 3107-3110. PMID 7593409 DOI: 10.1210/Jcem.80.11.7593409 |
0.342 |
|
| 1995 |
Ho C, Conner DA, Pollak MR, Ladd DJ, Kifor O, Warren HB, Brown EM, Seidman JG, Seidman CE. A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism Nature Genetics. 11: 389-394. PMID 7493018 DOI: 10.1038/Ng1295-389 |
0.355 |
|
| 1995 |
Pollak MR, Chou YW, Marx SJ, Steinmann B, Cole DEC, Brandi ML, Papapoulos SE, Menko FH, Hendy GN, Brown EM, Seidman CE, Seidman JG. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism Pediatric Nephrology. 9: 297-297. DOI: 10.1016/B978-0-12-397166-1.00024-2 |
0.364 |
|
| 1994 |
Pollak MR, Chou YHW, Marx SJ, Steinmann B, Cole DEC, Brandi ML, Papapoulos SE, Menko FH, Hendy GN, Brown EM, Seidman CE, Seidman JG. Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism: Effects of mutant gene dosage on phenotype Journal of Clinical Investigation. 93: 1108-1112. PMID 8132750 DOI: 10.1007/Bf02254188 |
0.313 |
|
| 1994 |
Pollak MR, Brown EM, Estep HL, McLaine PN, Kifor O, Park J, Hebert SC, Seidman CE, Seidman JG. Autosomal dominant hypocalcaemia caused by a Ca2+-sensing receptor gene mutation Nature Genetics. 8: 303-307. PMID 7874174 DOI: 10.1038/Ng1194-303 |
0.336 |
|
| 1994 |
Brown EM, Pollak M, Riccardi D, Hebert SC. Cloning and characterization of an extracellular Ca2+ -sensing receptor from parathyroid and kidney: new insights into the physiology and pathophysiology of calcium metabolism Nephrology Dialysis Transplantation. 9: 1703-1706. DOI: 10.1093/Ndt/9.12.1703 |
0.302 |
|
| 1993 |
Pollak MR, Brown EM, Chou YHW, Hebert SC, Marx SJ, Stelnmann B, Levi T, Seidman CE, Seidman JG. Mutations in the human Ca2+-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism Cell. 75: 1297-1303. PMID 7916660 DOI: 10.1016/0092-8674(93)90617-Y |
0.334 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2023 |
Pollak MR, Friedman DJ. APOL1 and APOL1-Associated Kidney Disease: A Common Disease, an Unusual Disease Gene - Proceedings of the Henry Shavelle Professorship. Glomerular Diseases. 3: 75-87. PMID 37113494 DOI: 10.1159/000529227 |
0.3 |
|
| 2014 |
Pollak MR, Quaggin SE, Hoenig MP, Dworkin LD. The glomerulus: the sphere of influence. Clinical Journal of the American Society of Nephrology : Cjasn. 9: 1461-9. PMID 24875196 DOI: 10.2215/Cjn.09400913 |
0.3 |
|
| 2020 |
Bar R, Ben-Shalom E, Duvdevani M, Belostotsky R, Pollak MR, Mount DB, Bar-Gal R, Gnessin E, Tzur S, Curhan GC, Frishberg Y. Mutations in do Not Confer a Dominant Phenotype Manifesting as Kidney Stone Disease. The Journal of Urology. 101097JU000000000000. PMID 33350326 DOI: 10.1097/JU.0000000000001528 |
0.299 |
|
| 2020 |
Feng D, Kumar M, Muntel J, Gurley SB, Birrane G, Stillman IE, Ding L, Wang MB, Ahmed S, Schlondorff J, Alper SL, Novak R, Ingber DE, Steen H, Pollak MR. Increased phosphorylation of ACTN4 leads to podocyte vulnerability and proteinuric kidney disease and is stimulated by high glucose and TGF‐b The Faseb Journal. 34: 1-1. DOI: 10.1096/Fasebj.2020.34.S1.02190 |
0.298 |
|
| 2005 |
Hunt JL, Pollak MR, Denker BM. Cultured podocytes establish a size-selective barrier regulated by specific signaling pathways and demonstrate synchronized barrier assembly in a calcium switch model of junction formation Journal of the American Society of Nephrology. 16: 1593-1602. PMID 15843471 DOI: 10.1681/Asn.2004080679 |
0.296 |
|
| 2019 |
Shao H, Wingert B, Weins A, Pollak MR, Camacho C, Wells A. Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutations. Scientific Reports. 9: 15517. PMID 31664084 DOI: 10.1038/S41598-019-51825-2 |
0.296 |
|
| 2010 |
Sun W, Sun W, Liu J, Zhou X, Xiao Y, Karaplis A, Pollak MR, Brown E, Goltzman D, Miao D. Alterations in phosphorus, calcium and PTHrP contribute to defects in dental and dental alveolar bone formation in calcium-sensing receptor-deficient mice. Development (Cambridge, England). 137: 985-92. PMID 20150282 DOI: 10.1242/Dev.045898 |
0.296 |
|
| 2009 |
Kantham L, Quinn SJ, Egbuna OI, Baxi K, Butters R, Pang JL, Pollak MR, Goltzman D, Brown EM. The calcium-sensing receptor (CaSR) defends against hypercalcemia independently of its regulation of parathyroid hormone secretion. American Journal of Physiology. Endocrinology and Metabolism. 297: E915-23. PMID 19797241 DOI: 10.1152/Ajpendo.00315.2009 |
0.295 |
|
| 1994 |
Brown EM, Pollak M, Hebert SC. Cloning and Characterization of Extracellular Ca 2+-Sensing Receptors from Parathyroid and Kidney The Endocrinologist. 4: 419-428. DOI: 10.1097/00019616-199411000-00004 |
0.292 |
|
| 2010 |
Feng J, Petersen CD, Coy DH, Jiang JK, Thomas CJ, Pollak MR, Wank SA. Calcium-sensing receptor is a physiologic multimodal chemosensor regulating gastric G-cell growth and gastrin secretion. Proceedings of the National Academy of Sciences of the United States of America. 107: 17791-6. PMID 20876097 DOI: 10.1073/Pnas.1009078107 |
0.291 |
|
| 2015 |
Ehrlicher AJ, Krishnan R, Guo M, Bidan CM, Weitz DA, Pollak MR. Alpha-actinin binding kinetics modulate cellular dynamics and force generation. Proceedings of the National Academy of Sciences of the United States of America. 112: 6619-24. PMID 25918384 DOI: 10.1073/Pnas.1505652112 |
0.291 |
|
| 2013 |
Quinn SJ, Thomsen ARB, Egbuna O, Pang J, Baxi K, Goltzman D, Pollak M, Brown EM. CaSR-mediated interactions between calcium and magnesium homeostasis in mice American Journal of Physiology - Endocrinology and Metabolism. 304: E724-E733. PMID 23360827 DOI: 10.1152/Ajpendo.00557.2012 |
0.291 |
|
| 2020 |
Berrigan M, Austrie J, Fleishman A, Tercyak KP, Pollak MR, Pavlakis M, Rohan V, Baliga PK, Kayler LK, Feeley TH, Rodrigue JR. Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantation. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. PMID 32659871 DOI: 10.1111/Ajt.16206 |
0.289 |
|
| 2006 |
Ardeshirpour L, Dann P, Pollak M, Wysolmerski J, VanHouten J. The calcium-sensing receptor regulates PTHrP production and calcium transport in the lactating mammary gland Bone. 38: 787-793. PMID 16377269 DOI: 10.1016/J.Bone.2005.11.009 |
0.287 |
|
| 1993 |
Pollak MR, Chou YHW, Cerda JJ, Steinmann B, La Du BN, Seidman JG, Seidman CE. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2 Nature Genetics. 5: 201-204. PMID 8252048 DOI: 10.1038/Ng1093-201 |
0.287 |
|
| 2000 |
Olszak IT, Poznansky MC, Evans RH, Olson D, Kos C, Pollak MR, Brown EM, Scadden DT. Extracellular calcium elicits a chemokinetic response from monocytes in vitro and in vivo Journal of Clinical Investigation. 105: 1299-1305. PMID 10792005 DOI: 10.1172/Jci9799 |
0.286 |
|
| 2016 |
Pollak M. Genetics of Familial FSGS. Seminars in Nephrology. 36: 467-472. PMID 27987547 DOI: 10.1016/J.Semnephrol.2016.09.010 |
0.286 |
|
| 1995 |
Brown EM, Pollak M, Seidman CE, Seidman JG, Chou YHW, Riccardi D, Hebert SC. Calcium-ion-sensing cell-surface receptors New England Journal of Medicine. 333: 234-240. PMID 7791841 DOI: 10.1056/Nejm199507273330407 |
0.282 |
|
| 2010 |
Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Uscinski AL, Higgs HN, Henderson JM, Pollak MR. Erratum: Corrigendum: Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis Nature Genetics. 42: 361-361. DOI: 10.1038/Ng0410-361B |
0.281 |
|
| 2008 |
Lee SH, Weins A, Hayes DB, Pollak MR, Dominguez R. Crystal structure of the actin-binding domain of alpha-actinin-4 Lys255Glu mutant implicated in focal segmental glomerulosclerosis. Journal of Molecular Biology. 376: 317-24. PMID 18164029 DOI: 10.1016/J.Jmb.2007.11.084 |
0.28 |
|
| 2010 |
Genovese G, Leibon G, Pollak MR, Rockmore DN. Improved IBD detection using incomplete haplotype information. Bmc Genetics. 11: 58. PMID 20591167 DOI: 10.1186/1471-2156-11-58 |
0.279 |
|
| 2013 |
Quinn SJ, Thomsen ARB, Pang JL, Kantham L, Bräuner-Osborne H, Pollak M, Goltzman D, Brown EM. Interactions between calcium and phosphorus in the regulation of the production of fibroblast growth factor 23 in vivo American Journal of Physiology - Endocrinology and Metabolism. 304: E310-E320. PMID 23233539 DOI: 10.1152/Ajpendo.00460.2012 |
0.278 |
|
| 2010 |
Parikh SM, Pollak MR. VEGF receptors and glomerular function. Journal of the American Society of Nephrology : Jasn. 21: 1599-600. PMID 20847145 DOI: 10.1681/Asn.2010080871 |
0.277 |
|
| 2013 |
Genovese G, Handsaker RE, Li H, Altemose N, Lindgren AM, Chambert K, Pasaniuc B, Price AL, Reich D, Morton CC, Pollak MR, Wilson JG, McCarroll SA. Using population admixture to help complete maps of the human genome. Nature Genetics. 45: 406-14, 414e1-2. PMID 23435088 DOI: 10.1038/Ng.2565 |
0.269 |
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| 2006 |
Adams GB, Chabner KT, Alley IR, Olson DP, Szczepiorkowski ZM, Poznansky MC, Kos CH, Pollak MR, Brown EM, Scadden DT. Stem cell engraftment at the endosteal niche is specified by the calcium-sensing receptor. Nature. 439: 599-603. PMID 16382241 DOI: 10.1038/Nature04247 |
0.268 |
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| 2012 |
Xue Y, Xiao Y, Liu J, Karaplis AC, Pollak MR, Brown EM, Miao D, Goltzman D. The calcium-sensing receptor complements parathyroid hormone-induced bone turnover in discrete skeletal compartments in mice. American Journal of Physiology. Endocrinology and Metabolism. 302: E841-51. PMID 22275754 DOI: 10.1152/Ajpendo.00599.2011 |
0.268 |
|
| 2008 |
Forman JP, Fisher ND, Pollak MR, Cox DG, Tonna S, Curhan GC. Renin-angiotensin system polymorphisms and risk of hypertension: influence of environmental factors. Journal of Clinical Hypertension (Greenwich, Conn.). 10: 459-66. PMID 18550936 DOI: 10.1111/J.1751-7176.2008.08007.X |
0.267 |
|
| 2007 |
Weins A, Schlondorff JS, Nakamura F, Pollak MR. 234 American Journal of Kidney Diseases. 49: B83. DOI: 10.1053/J.Ajkd.2007.02.242 |
0.265 |
|
| 2007 |
Chattopadhyay N, Jeong KH, Yano S, Huang S, Pang JL, Ren X, Terwilliger E, Kaiser UB, Vassilev PM, Pollak MR, Brown EM. Calcium receptor stimulates chemotaxis and secretion of MCP-1 in GnRH neurons in vitro: potential impact on reduced GnRH neuron population in CaR-null mice. American Journal of Physiology. Endocrinology and Metabolism. 292: E523-32. PMID 17003237 DOI: 10.1152/Ajpendo.00372.2005 |
0.265 |
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| 2023 |
Egbuna O, Zimmerman B, Manos G, Fortier A, Chirieac MC, Dakin LA, Friedman DJ, Bramham K, Campbell K, Knebelmann B, Barisoni L, Falk RJ, Gipson DS, Lipkowitz MS, Ojo A, ... ... Pollak MR, et al. Inaxaplin for Proteinuric Kidney Disease in Persons with Two Variants. The New England Journal of Medicine. 388: 969-979. PMID 36920755 DOI: 10.1056/NEJMoa2202396 |
0.265 |
|
| 2015 |
Heneghan JF, Vandorpe DH, Shmukler BE, Giovinnazo JA, Raper J, Friedman DJ, Pollak MR, Alper SL. BH3 domain-independent apolipoprotein L1 toxicity rescued by BCL2 prosurvival proteins. American Journal of Physiology. Cell Physiology. 309: C332-47. PMID 26108665 DOI: 10.1152/Ajpcell.00142.2015 |
0.265 |
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| 2021 |
Weng PL, Majmundar AJ, Khan K, Lim TY, Shril S, Jin G, Musgrove J, Wang M, Ahram DF, Aggarwal VS, Bier LE, Heinzen EL, Onuchic-Whitford AC, Mann N, Buerger F, ... ... Pollak MR, et al. De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis. American Journal of Human Genetics. PMID 33508234 DOI: 10.1016/j.ajhg.2021.01.008 |
0.263 |
|
| 2011 |
Shu L, Ji J, Zhu Q, Cao G, Karaplis A, Pollak MR, Brown E, Goltzman D, Miao D. The calcium-sensing receptor mediates bone turnover induced by dietary calcium and parathyroid hormone in neonates. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 26: 1057-71. PMID 21542007 DOI: 10.1002/Jbmr.300 |
0.262 |
|
| 2005 |
Leykin I, Hao K, Cheng J, Meyer N, Pollak MR, Smith RJ, Wong WH, Rosenow C, Li C. Comparative linkage analysis and visualization of high-density oligonucleotide SNP array data. Bmc Genetics. 6: 7. PMID 15713228 DOI: 10.1186/1471-2156-6-7 |
0.262 |
|
| 2010 |
Rhee EP, Souza A, Farrell L, Pollak MR, Lewis GD, Steele DJ, Thadhani R, Clish CB, Greka A, Gerszten RE. Metabolite profiling identifies markers of uremia. Journal of the American Society of Nephrology : Jasn. 21: 1041-1051. PMID 20378825 DOI: 10.1681/Asn.2009111132 |
0.261 |
|
| 2010 |
Gu C, Yaddanapudi S, Weins A, Osborn T, Reiser J, Pollak M, Hartwig J, Sever S. Direct dynamin-actin interactions regulate the actin cytoskeleton. The Embo Journal. 29: 3593-606. PMID 20935625 DOI: 10.1038/Emboj.2010.249 |
0.26 |
|
| 2012 |
Carrasquillo R, Tian D, Krishna S, Pollak MR, Greka A, Schlöndorff J. SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activity. Bmc Cell Biology. 13: 33. PMID 23171048 DOI: 10.1186/1471-2121-13-33 |
0.257 |
|
| 2016 |
Shukha K, Mueller JL, Chung RT, Curry MP, Friedman DJ, Pollak MR, Berg AH. Most ApoL1 Is Secreted by the Liver. Journal of the American Society of Nephrology : Jasn. PMID 27932478 DOI: 10.1681/Asn.2016040441 |
0.254 |
|
| 2010 |
Shao H, Wang JH, Pollak MR, Wells A. α-actinin-4 is essential for maintaining the spreading, motility and contractility of fibroblasts. Plos One. 5: e13921. PMID 21085685 DOI: 10.1371/Journal.Pone.0013921 |
0.251 |
|
| 2022 |
Karp S, Pollak MR, Subramanian B. Disease Modeling with Kidney Organoids. Micromachines. 13. PMID 36144007 DOI: 10.3390/mi13091384 |
0.24 |
|
| 2023 |
Gupta Y, Friedman DJ, McNulty M, Khan A, Lane B, Wang C, Ke J, Jin G, Wooden B, Knob AL, Lim TY, Appel GB, Huggins K, Liu L, Mitrotti A, ... ... Pollak MR, et al. Strong protective effect of the p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37577628 DOI: 10.1101/2023.08.02.23293554 |
0.239 |
|
| 2012 |
Zhang X, Giovannucci EL, Wu K, Smith-Warner SA, Fuchs CS, Pollak MR, Willett WC, Ma J. Magnesium intake, plasma C-peptide, and colorectal cancer incidence in US women: a 28-year follow-up study British Journal of Cancer. 106: 1335-1341. PMID 22415230 DOI: 10.1038/Bjc.2012.76 |
0.237 |
|
| 2023 |
Gupta Y, Friedman DJ, McNulty MT, Khan A, Lane B, Wang C, Ke J, Jin G, Wooden B, Knob AL, Lim TY, Appel GB, Huggins K, Liu L, Mitrotti A, ... ... Pollak MR, et al. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Nature Communications. 14: 7836. PMID 38036523 DOI: 10.1038/s41467-023-43020-9 |
0.236 |
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| 2022 |
Nadkarni GN, Fei K, Ramos MA, Hauser D, Bagiella E, Ellis SB, Sanderson S, Scott SA, Sabin T, Madden E, Cooper R, Pollak M, Calman N, Bottinger EP, Horowitz CR. Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial. Jama Network Open. 5: e221048. PMID 35244702 DOI: 10.1001/jamanetworkopen.2022.1048 |
0.229 |
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| 2022 |
Riella CV, McNulty M, Ribas GT, Tattersfield CF, Perez-Gill C, Eichinger F, Kelly J, Chun J, Subramanian B, Guizelini D, Alper SL, Pollak MR, Sampson MG, Friedman DJ. ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuit. Proceedings of the National Academy of Sciences of the United States of America. 119: e2210150119. PMID 36282916 DOI: 10.1073/pnas.2210150119 |
0.229 |
|
| 2014 |
Pollak MR. Familial FSGS. Advances in Chronic Kidney Disease. 21: 422-5. PMID 25168831 DOI: 10.1053/j.ackd.2014.06.001 |
0.228 |
|
| 2009 |
Gualberto A, Dolled-Filhart MP, Hixon ML, Christensen J, Rimm DL, Lee AV, Wang Y, Pollak M, Paz-Ares LG, Karp DD. Molecular bases for sensitivity to figitumumab (CP-751,871) in NSCLC. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 27: 8091. PMID 27962669 DOI: 10.1200/Jco.2009.27.15_Suppl.8091 |
0.227 |
|
| 2022 |
Milosavljevic J, Lempicki C, Lang K, Heinkele H, Kampf L, Leroy C, Chen M, Gerstner L, Spitz D, Wang M, Knob A, Kayser S, Helmstädter M, Walz G, Pollak M, et al. Nephrotic Syndrome Gene is Required for Endosomal Maturation and Nephrin Endocytosis in . Journal of the American Society of Nephrology : Jasn. PMID 36137753 DOI: 10.1681/ASN.2022030275 |
0.224 |
|
| 2015 |
Allen DB, Backeljauw P, Bidlingmaier M, Biller B, Boguszewski M, Burman P, Butler G, Chihara K, Christiansen JS, Cianfarani S, Clayton PE, Clemmons D, Cohen P, Darendeliler F, Deal C, ... ... Pollak M, et al. Growth Hormone Safety Workshop Position Paper: a critical appraisal of recombinant human growth hormone therapy in children and adults. European Journal of Endocrinology / European Federation of Endocrine Societies. PMID 26563978 DOI: 10.1530/Eje-15-0873 |
0.221 |
|
| 2004 |
Diorio C, Pollak M, Byrne C, Mâsse B, Côté G, Hébert-Croteau N, Yaffe M, Bérubé S, Morin C, Brisson J. Insulin-like growth factor-I (IGF-I), IGF-binding protein-3 (IGFBP-3), and mammographic breast density Journal of Clinical Oncology. 22: 9501-9501. DOI: 10.1200/Jco.2004.22.90140.9501 |
0.218 |
|
| 2022 |
Chun J, Riella C, Chung H, Shah S, Wang M, Magraner J, Ribas G, Ribas H, Zhang JY, Alper S, Friedman D, Pollak M. DGAT2 Inhibition Potentiates Lipid Droplet Formation to Reduce Cytotoxicity in APOL1 Kidney Risk Variants. Journal of the American Society of Nephrology : Jasn. PMID 35232775 DOI: 10.1681/ASN.2021050723 |
0.216 |
|
| 2023 |
Barry A, McNulty MT, Jia X, Gupta Y, Debiec H, Luo Y, Nagano C, Horinouchi T, Jung S, Colucci M, Ahram DF, Mitrotti A, Sinha A, Teeninga N, Jin G, ... ... Pollak MR, et al. Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Nature Communications. 14: 2481. PMID 37120605 DOI: 10.1038/s41467-023-37985-w |
0.215 |
|
| 2010 |
Broedersz CP, Depken M, Yao NY, Pollak MR, Weitz DA, MacKintosh FC. Cross-link-governed dynamics of biopolymer networks. Physical Review Letters. 105: 238101. PMID 21231506 DOI: 10.1103/Physrevlett.105.238101 |
0.214 |
|
| 2004 |
Fuchs C, Pollak M, Sargent DJ, Meyerhardt JA, Ramanathan RK, Williamson S, Findlay B, Green E, Goldberg RM. Insulin-like growth factor-I (IGF-1), IGF binding protein-3 (IGFBP-3), and outcome in metastatic colorectal cancer (CRC): Results from Intergroup Trial N9741 Journal of Clinical Oncology. 22: 3521-3521. DOI: 10.1200/Jco.2004.22.90140.3521 |
0.213 |
|
| 2009 |
Hixon ML, Gualberto A, Demers L, Paz-Ares LG, Novello S, Blakely LJ, Langer CL, Lipton A, Pollak M, Karp DD. Correlation of plasma levels of free insulin-like growth factor 1 and clinical benefit of the IGF-IR inhibitor figitumumab (CP- 751, 871). Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 27: 3539. PMID 27961330 DOI: 10.1200/Jco.2009.27.15_Suppl.3539 |
0.213 |
|
| 2013 |
Yao NY, Broedersz CP, Depken M, Becker DJ, Pollak MR, Mackintosh FC, Weitz DA. Stress-enhanced gelation: a dynamic nonlinearity of elasticity. Physical Review Letters. 110: 018103. PMID 23383843 DOI: 10.1103/Physrevlett.110.018103 |
0.21 |
|
| 2021 |
Lane BM, Murray S, Benson K, Bierzynska A, Chryst-Stangl M, Wang L, Wu G, Cavalleri G, Doyle B, Fennelly N, Dorman A, Conlon S, Vega-Warner V, Fermin D, Vijayan P, ... ... Pollak M, et al. A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 () Gene Confers Enhanced Calcineurin Activity and May Cause FSGS. Journal of the American Society of Nephrology : Jasn. PMID 33863784 DOI: 10.1681/ASN.2020081234 |
0.209 |
|
| 2022 |
Vandorpe DH, Heneghan JF, Waitzman JS, McCarthy GM, Blasio A, Magraner JM, Donovan OG, Schaller LB, Shah SS, Subramanian B, Riella CV, Friedman DJ, Pollak MR, Alper SL. Apolipoprotein L1 (APOL1) cation current in HEK-293 cells and in human podocytes. Pflugers Archiv : European Journal of Physiology. PMID 36449077 DOI: 10.1007/s00424-022-02767-8 |
0.208 |
|
| 2021 |
Bhargava R, Lehoux S, Maeda K, Tsokos MG, Krishfield S, Ellezian LY, Pollak M, Stillman IE, Cummings RD, Tsokos GC. Aberrantly glycosylated IgG elicits pathogenic signaling in podocytes and signifies lupus nephritis. Jci Insight. PMID 33784256 DOI: 10.1172/jci.insight.147789 |
0.206 |
|
| 2024 |
Cunanan J, Rajyam SS, Sharif B, Udwan K, Rana A, De Gregorio V, Ricardo S, Elia A, Brooks B, Weins A, Pollak M, John R, Barua M. Mice with a missense variant display impaired glomerular repair. American Journal of Physiology. Renal Physiology. PMID 38482556 DOI: 10.1152/ajprenal.00259.2023 |
0.205 |
|
| 2014 |
Rotimi C, Abayomi A, Abimiku A, Adabayeri VM, Adebamowo C, Adebiyi E, Ademola AD, Adeyemo A, Adu D, Affolabi D, Agongo G, Ajayi S, Akarolo-Anthony S, Akinyemi R, ... ... Pollak M, et al. Research capacity. Enabling the genomic revolution in Africa. Science (New York, N.Y.). 344: 1346-8. PMID 24948725 DOI: 10.1126/Science.1251546 |
0.203 |
|
| 2023 |
Lemire G, Sanchis-Juan A, Russell K, Baxter S, Chao KR, Singer-Berk M, Groopman E, Wong I, England E, Goodrich J, Pais L, Austin-Tse C, DiTroia S, O'Heir E, Ganesh VS, ... ... Pollak MR, et al. Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37873196 DOI: 10.1101/2023.10.05.23296595 |
0.202 |
|
| 2009 |
Ali SM, Chapman JW, Demers L, Shepherd L, Han L, Wilson C, Pritchard K, Leitzel K, Pollak M, Lipton A. Effect of adjuvant chemotherapy on bone resorption marker beta C-telopeptide (B-CTX) in postmenopausal women. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 27: 594. PMID 27960704 DOI: 10.1200/Jco.2009.27.15_Suppl.594 |
0.198 |
|
| 2020 |
Sun H, Perez-Gill C, Schlöndorff JS, Subramanian B, Pollak MR. Dysregulated Dynein-mediated Trafficking of Nephrin Causes INF2-related Podocytopathy. Journal of the American Society of Nephrology : Jasn. PMID 33443052 DOI: 10.1681/ASN.2020081109 |
0.194 |
|
| 2008 |
Weins A, Pollak MR. Inherited nephroses Molecular and Genetic Basis of Renal Disease. 141-150. DOI: 10.1016/B978-1-4160-0252-9.50013-6 |
0.192 |
|
| 2021 |
McNulty MT, Fermin D, Eichinger F, Jang D, Kretzler M, Burtt N, Pollak MR, Flannick J, Weins A, Friedman DJ, Sampson MG. A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis. Kidney International. PMID 34929253 DOI: 10.1016/j.kint.2021.10.041 |
0.19 |
|
| 2022 |
Harris DD, Fleishman A, Pavlakis M, Pollak MR, Baliga PK, Rohan V, Kayler LK, Rodrigue JR. Apolipoprotein L1 Opinions of African American Living Kidney Donors, Kidney Transplant Patients, and Nonpatients. The Journal of Surgical Research. 277: 116-124. PMID 35489216 DOI: 10.1016/j.jss.2022.04.011 |
0.181 |
|
| 2014 |
Barua M, Pollak MR. Focal and segmental glomerulosclerosis Core Concepts in Parenchymal Kidney Disease. 2147483647: 33-49. DOI: 10.1007/978-1-4614-8166-9_4 |
0.178 |
|
| 2020 |
Hoenig MP, Steinman TI, Pollak MR, Zeidel ML. In Memorium: Burton Rose, 1942-2020. Journal of the American Society of Nephrology : Jasn. PMID 32527976 DOI: 10.1681/Asn.2020050702 |
0.178 |
|
| 2021 |
McCarthy GM, Blasio A, Donovan OG, Schaller LB, Bock-Hughes A, Magraner JM, Suh JH, Tattersfield CF, Stillman IE, Shah SS, Zsengeller ZK, Subramanian B, Friedman DJ, Pollak MR. Recessive, gain-of-function toxicity in an APOL1 BAC transgenic mouse model mirrors human APOL1 kidney disease. Disease Models & Mechanisms. 14. PMID 34350953 DOI: 10.1242/dmm.048952 |
0.171 |
|
| 2021 |
Nadkarni GN, Fei K, Galarneau G, Gao Y, Wilson JG, Cooper R, Madden EB, Denny JC, Richardson LD, Pollak M, Loos RJF, Horowitz CR. APOL1 renal risk variants are associated with obesity and body composition in African ancestry adults: An observational genotype-phenotype association study. Medicine. 100: e27785. PMID 34766590 DOI: 10.1097/MD.0000000000027785 |
0.167 |
|
| 2014 |
Gładysz S, Li X, Kong X, Yu X, Zhu Y, Xing C, Mao H, Wu B, Yan W, Stubnova V, Os I, Grundtvig M, Atar D, Waldum-Grevbo B, Lou L, ... ... Pollak MR, et al. Front & Back Matter Cardiorenal Medicine. 4. DOI: 10.1159/000362632 |
0.167 |
|
| 2022 |
Lieberman KV, Chang AR, Block GA, Robinson K, Bristow SL, Morales A, Mitchell A, McCalley S, McKay J, Pollak MR, Aradhya S, Warady BA. The KIDNEYCODE Program: Diagnostic Yield and Clinical Features of Individuals with CKD. Kidney360. 3: 900-909. PMID 36128480 DOI: 10.34067/KID.0004162021 |
0.163 |
|
| 2008 |
Pollak MR, Mount DB. The impact of molecular genetics on nephrology Molecular and Genetic Basis of Renal Disease. 1-2. DOI: 10.1016/B978-1-4160-0252-9.50005-7 |
0.135 |
|
| 2022 |
Morales-Alvarez MC, Knob A, Rennke HG, Pollak MR, Denker BM. Clinical and Pathological Heterogeneity in FSGS due to Mutations. Kidney International Reports. 7: 2741-2745. PMID 36506246 DOI: 10.1016/j.ekir.2022.08.033 |
0.133 |
|
| 2021 |
Williams S, Charest J, Pollak M, Subramanian BK. Bioengineering Strategies To Develop Podocyte Culture Systems. Tissue Engineering. Part B, Reviews. PMID 34541902 DOI: 10.1089/ten.TEB.2021.0154 |
0.125 |
|
| 2024 |
Lemire G, Sanchis-Juan A, Russell K, Baxter S, Chao KR, Singer-Berk M, Groopman E, Wong I, England E, Goodrich J, Pais L, Austin-Tse C, DiTroia S, O'Heir E, Ganesh VS, ... ... Pollak MR, et al. Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease. American Journal of Human Genetics. PMID 38565148 DOI: 10.1016/j.ajhg.2024.03.008 |
0.12 |
|
| 2024 |
Gbadegesin R, Martinelli E, Gupta Y, Friedman DJ, Sampson MG, Pollak MR, Sanna-Cherchi S. Genotyping Is Incomplete without Testing for the Protective M1 Modifier p.N264K Variant. Glomerular Diseases. 4: 43-48. PMID 38495868 DOI: 10.1159/000537948 |
0.12 |
|
| 1997 |
Pollak MR, Brown EM. Chapter 8 Molecular aspects of familial hypocalciuric hypercalcemia Advances in Molecular and Cellular Endocrinology. 1: 229-239. DOI: 10.1016/S1569-2566(97)80039-7 |
0.082 |
|
| 2000 |
Tsukaguchi H, Yager H, Dawborn J, Jost L, Cohlmia J, Abreu PF, Pereira AB, Pollak MR. A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31. Journal of the American Society of Nephrology : Jasn. 11: 1674-80. PMID 10966492 |
0.077 |
|
| 1984 |
Pollak MR, Schuler RH. Numerical treatment of the kinetics of track processes in radiation chemistry Radiation Physics and Chemistry. 23: 285-291. DOI: 10.1016/0146-5724(84)90121-3 |
0.049 |
|
| 2021 |
Běhálek L, Dobránsky J, Pollák M, Borůvka M, Brdlík P. Application of Physical Methods for the Detection of a Thermally Degraded Recycled Material in Plastic Parts Made of Polypropylene Copolymer. Materials (Basel, Switzerland). 14. PMID 33498867 DOI: 10.3390/ma14030552 |
0.028 |
|
| 2009 |
Lipton A, Chapman J, Demers L, Shepherd L, Han L, Wilson C, Pritchard K, Leitzel K, Ali S, Pollak M. 0068 Elevated bone resorption predicts shorter recurrence-free survival (RFS) for bone metastasis in breast cancer (BC) The Breast. 18: S35. DOI: 10.1016/S0960-9776(09)70113-4 |
0.026 |
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