IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23

[1]  M. Hughson,et al.  Mesangial proliferative glomerulonephritis in southwestern American Indians. , 1993, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[2]  F. Schena.  A retrospective analysis of the natural history of primary IgA nephropathy worldwide. , 1990, The American journal of medicine.

[3]  B. Julian,et al.  Familial IgA nephropathy. Evidence of an inherited mechanism of disease. , 1985, The New England journal of medicine.

[4]  B. Julian,et al.  IgA nephropathy, the most common glomerulonephritis worldwide. A neglected disease in the United States? , 1988, The American journal of medicine.

[5]  F. Schena,et al.  IgA nephropathy: pros and cons for a familial disease. , 1993, Contributions to nephrology.

[6]  J. Ward,et al.  Uteroglobin is essential in preventing immunoglobulin A nephropathy in mice , 1999, Nature Medicine.

[7]  R. Lifton,et al.  Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter , 1996, Nature Genetics.

[8]  D. Gerhard,et al.  Human uteroglobin gene: structure, subchromosomal localization, and polymorphism. , 1997, DNA and cell biology.

[9]  L Kruglyak,et al.  Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.

[10]  G. Hitman,et al.  HLA-DQ gene polymorphism in primary IgA nephropathy in three European populations. , 1996, Kidney international.

[11]  B. Julian,et al.  Regionalization in hereditary IgA nephropathy. , 1987, American journal of human genetics.

[12]  R. Scott,et al.  Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27. , 1998, Human molecular genetics.

[13]  J. D. de Fijter,et al.  Reduced binding of immunoglobulin A (IgA) from patients with primary IgA nephropathy to the myeloid IgA Fc-receptor, CD89. , 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[14]  G. D'Amico,et al.  The commonest glomerulonephritis in the world: IgA nephropathy. , 1987, The Quarterly journal of medicine.

[15]  J. Stephens,et al.  Mapping by admixture linkage disequilibrium in human populations: limits and guidelines. , 1994, American journal of human genetics.

[16]  M. Endoh,et al.  Polymorphism in the Iα1 Germ-Line Transcript Regulatory Region and IgA Productivity in Patients with IgA Nephropathy , 1998, The Journal of Immunology.

[17]  L. Ibels,et al.  IgA Nephropathy: Analysis of the Natural History, Important Factors in the Progression of Renal Disease, and a Review of the Literature , 1994, Medicine.

[18]  E. Lander,et al.  Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results , 1995, Nature Genetics.

[19]  J. Terwilliger.  A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. , 1995, American journal of human genetics.

[20]  S. Wall,et al.  Low incidence of IgA nephropathy in blacks. , 1985, Kidney international.

[21]  G. Lathrop,et al.  Easy calculations of lod scores and genetic risks on small computers. , 1984, American journal of human genetics.

[22]  F. Schena.  Immunogenetic aspects of primary IgA nephropathy. , 1995, Kidney international.

[23]  E. Jones,et al.  Distribution of primary renal diseases leading to end-stage renal failure in the United States, Europe, and Australia/New Zealand: results from an international comparative study. , 2000, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[24]  F. Scolari,et al.  Familial clustering of IgA nephropathy: further evidence in an Italian population. , 1999, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[25]  B. Julian,et al.  Progress in the pathogenesis of IgA nephropathy. , 1999, Advances in nephrology from the Necker Hospital.

[26]  P. Zucchelli,et al.  [IgA nephropathy]. , 1985, Medicina clinica.

[27]  F. Scolari,et al.  Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors. , 1992, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[28]  H. Oksa,et al.  Immunoglobulin and complement deposition in glomeruli of 756 subjects who had committed suicide or met with a violent death. , 1993, Journal of clinical pathology.

[29]  J J Faraway,et al.  Distribution of the admixture test for the detection of linkage under heterogeneity , 1993, Genetic epidemiology.

[30]  S. Harper,et al.  Nephrology Dialysis Transplantation Leucocyte B1,3 Galactosyltransferase Activity in Iga Nephropathy , 2022 .