Harvard Catalyst Profiles

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Andrzej Stefan Krolewski, Ph.D., M.D.

Co-Author

This page shows the publications co-authored by Andrzej Krolewski and Alessandro Doria.
Connection Strength

4.314
  1. Diabetes: Lowering serum uric acid levels to prevent kidney failure. Nat Rev Nephrol. 2011 Aug 02; 7(9):495-6.
    View in: PubMed
    Score: 0.475
  2. Comprehensive Search for Novel Circulating miRNAs and Axon Guidance Pathway Proteins Associated with Risk of ESKD in Diabetes. J Am Soc Nephrol. 2021 09; 32(9):2331-2351.
    View in: PubMed
    Score: 0.236
  3. A signature of circulating inflammatory proteins and development of end-stage renal disease in diabetes. Nat Med. 2019 05; 25(5):805-813.
    View in: PubMed
    Score: 0.203
  4. Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes. Diabetes Care. 1999 Feb; 22(2):253-61.
    View in: PubMed
    Score: 0.200
  5. Synergistic effect of angiotensin II type 1 receptor genotype and poor glycaemic control on risk of nephropathy in IDDM. Diabetologia. 1997 Nov; 40(11):1293-9.
    View in: PubMed
    Score: 0.183
  6. Improved clinical trial enrollment criterion to identify patients with diabetes at risk of end-stage renal disease. Kidney Int. 2017 07; 92(1):258-266.
    View in: PubMed
    Score: 0.176
  7. Diabetes susceptibility at IDDM2 cannot be positively mapped to the VNTR locus of the insulin gene. Diabetologia. 1996 May; 39(5):594-9.
    View in: PubMed
    Score: 0.165
  8. Angiotensinogen polymorphism M235T, hypertension, and nephropathy in insulin-dependent diabetes. Hypertension. 1996 May; 27(5):1134-9.
    View in: PubMed
    Score: 0.165
  9. Genetic susceptibility to nephropathy in insulin-dependent diabetes: from epidemiology to molecular genetics. Diabetes Metab Rev. 1995 Dec; 11(4):287-314.
    View in: PubMed
    Score: 0.160
  10. Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16q. Diabetes. 1995 Feb; 44(2):243-7.
    View in: PubMed
    Score: 0.151
  11. DdeI polymorphism in the AGTR1 gene. Hum Mol Genet. 1994 Aug; 3(8):1444.
    View in: PubMed
    Score: 0.146
  12. Angiotensin I-converting enzyme (ACE): estimation of DNA haplotypes in unrelated individuals using denaturing gradient gel blots. Hum Genet. 1994 Aug; 94(2):117-23.
    View in: PubMed
    Score: 0.146
  13. Genetic predisposition to diabetic nephropathy. Evidence for a role of the angiotensin I--converting enzyme gene. Diabetes. 1994 May; 43(5):690-5.
    View in: PubMed
    Score: 0.144
  14. Molecular characterization of a DDEI melting polymorphism at the angiotensin I-converting enzyme (ACE) locus. Hum Mutat. 1994; 4(2):155-7.
    View in: PubMed
    Score: 0.141
  15. Four RSAI restriction fragment melting polymorphisms in the region of the insulin receptor gene encoding for the alpha subunit. Clin Genet. 1993 Nov; 44(5):279-80.
    View in: PubMed
    Score: 0.139
  16. Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes. JAMA. 2013 Aug 28; 310(8):821-8.
    View in: PubMed
    Score: 0.137
  17. Early progressive renal decline precedes the onset of microalbuminuria and its progression to macroalbuminuria. Diabetes Care. 2014; 37(1):226-34.
    View in: PubMed
    Score: 0.137
  18. Circulating TNF receptors 1 and 2 predict ESRD in type 2 diabetes. J Am Soc Nephrol. 2012 Mar; 23(3):507-15.
    View in: PubMed
    Score: 0.123
  19. High-normal serum uric acid increases risk of early progressive renal function loss in type 1 diabetes: results of a 6-year follow-up. Diabetes Care. 2010 Jun; 33(6):1337-43.
    View in: PubMed
    Score: 0.108
  20. Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction. Proc Natl Acad Sci U S A. 2009 Aug 25; 106(34):14460-5.
    View in: PubMed
    Score: 0.104
  21. Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes. Diabetes. 2009 Jun; 58(6):1403-10.
    View in: PubMed
    Score: 0.100
  22. Identification of a locus modulating serum C-reactive protein levels on chromosome 5p15. Atherosclerosis. 2008 Feb; 196(2):863-70.
    View in: PubMed
    Score: 0.088
  23. Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY loci on chromosome 8p23. Ann Hum Genet. 2006 Sep; 70(Pt 5):587-93.
    View in: PubMed
    Score: 0.085
  24. Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23. Diabetes. 2004 May; 53(5):1375-84.
    View in: PubMed
    Score: 0.072
  25. Genetic modifiers of the age at diagnosis of diabetes (MODY3) in carriers of hepatocyte nuclear factor-1alpha mutations map to chromosomes 5p15, 9q22, and 14q24. Diabetes. 2003 Aug; 52(8):2182-6.
    View in: PubMed
    Score: 0.068
  26. Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect. Diabetes Care. 2002 Dec; 25(12):2292-301.
    View in: PubMed
    Score: 0.065
  27. Mutation screening of the neurogenin-3 gene in autosomal dominant diabetes. J Clin Endocrinol Metab. 2001 May; 86(5):2320-2.
    View in: PubMed
    Score: 0.058
  28. Type 2 diabetes locus on 12q15. Further mapping and mutation screening of two candidate genes. Diabetes. 2001 Jan; 50(1):204-8.
    View in: PubMed
    Score: 0.057
  29. Evidence of a novel type 2 diabetes locus 50 cM centromeric to NIDDM2 on chromosome 12q. Diabetes. 1999 Nov; 48(11):2246-51.
    View in: PubMed
    Score: 0.053
  30. Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus. Nat Genet. 1999 Nov; 23(3):323-8.
    View in: PubMed
    Score: 0.053
  31. Hepatocyte nuclear factor-4gamma: cDNA sequence, gene organization, and mutation screening in early-onset autosomal-dominant type 2 diabetes. Diabetes. 1999 Oct; 48(10):2099-102.
    View in: PubMed
    Score: 0.052
  32. Exclusion of insulin receptor substrate 2 (IRS-2) as a major locus for early-onset autosomal dominant type 2 diabetes. Diabetes. 1999 Mar; 48(3):640-2.
    View in: PubMed
    Score: 0.050
  33. Codon 972 polymorphism in the insulin receptor substrate-1 gene, obesity, and risk of noninsulin-dependent diabetes mellitus. J Clin Endocrinol Metab. 1996 Apr; 81(4):1657-9.
    View in: PubMed
    Score: 0.041
  34. Molecular genetic approaches to the identification of genes involved in the development of nephropathy in insulin-dependent diabetes mellitus. J Am Soc Nephrol. 1992 Oct; 3(4 Suppl):S9-17.
    View in: PubMed
    Score: 0.032
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.