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» Authors » Florian Buerger

Florian Buerger

Explore the profile of Florian Buerger including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 27
Citations 167
Followers 0
Related Specialties
Nephrology
Genetics
Biochemistry
Top 10 Co-Authors
Friedhelm Hildebrandt
Shirlee Shril
Ronen Schneider
Amar J Majmundar
Verena Klambt
Nina Mann
Ana C Onuchic-Whitford
Richard P Lifton
Thomas M Kitzler
Daanya Salmanullah
Published In
J Am Soc Nephrol
Am J Hum Genet
J Nephrol
Kidney Int Rep
Genes Dis
Affiliations
Soon will be listed here.
Recent Articles
1.
Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome
Schneider R, Shril S, Buerger F, Deutsch K, Yousef K, Frank C, et al.
Genes Dis . 2024 Nov; 12(2):101280. PMID: 39584075
No abstract available.
2.
Correction to: Phenotypic quantification of Nphs1‑deficient mice
Schneider R, Mansour B, Kolvenbach C, Buerger F, Salmanullah D, Lemberg K, et al.
J Nephrol . 2024 Aug; 37(6):1723. PMID: 39115675
No abstract available.
3.
Phenotypic quantification of Nphs1-deficient mice
Schneider R, Mansour B, Kolvenbach C, Buerger F, Salmanullah D, Lemberg K, et al.
J Nephrol . 2024 Jul; 38(1):143-152. PMID: 39003671
Background: Steroid-resistant nephrotic syndrome (SRNS) is the second most frequent cause of chronic kidney disease in children and young adults. The most severe form of steroid-resistant nephrotic syndrome is congenital...
4.
Quantifiable and reproducible phenotypic assessment of a constitutive knockout mouse model for congenital nephrotic syndrome of the Finnish type
Lemberg K, Mertens N, Yousef K, Schneider R, Merz L, Mansour B, et al.
Sci Rep . 2024 Jul; 14(1):15916. PMID: 38987283
Steroid-resistant nephrotic syndrome (SRNS) is the second most frequent cause of childhood chronic kidney disease. Congenital nephrotic syndrome of the Finnish type (CNF) (MIM# 256300) is caused by biallelic variants...
5.
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding deletions
Deutsch K, Klambt V, Kitzler T, Jobst-Schwan T, Schneider R, Buerger F, et al.
Genes Dis . 2024 Jun; 11(5):101111. PMID: 38868576
No abstract available.
6.
Recessive variants in the intergenic locus cause monogenic kidney disease responsive to anti-proteinuric treatment
Buerger F, Salmanullah D, Liang L, Gauntner V, Krueger K, Qi M, et al.
medRxiv . 2024 Apr; PMID: 38562757
In genetic disease, an accurate expression landscape of disease genes and faithful animal models will enable precise genetic diagnoses and therapeutic discoveries, respectively. We previously discovered that variants in ,...
7.
Quantitative phenotyping of knockout mice as a prerequisite for gene replacement studies
Buerger F, Merz L, Saida K, Yu S, Salmanullah D, Lemberg K, et al.
Am J Physiol Renal Physiol . 2024 Mar; 326(5):F780-F791. PMID: 38482553
Steroid-resistant nephrotic syndrome (SRNS) is the second most frequent cause of chronic kidney disease before the age of 25 yr. Nephrin, encoded by localizes to the slit diaphragm of glomerular...
8.
Normothermic Ex Situ Machine Perfusion of Vascularized Composite Allografts with Oxygen Microcarriers for 12 Hours Using Real-Time Mitochondrial Redox Quantification
Haug V, Peng Y, Tchiloemba B, Wang A, Buerger F, Romfh P, et al.
J Clin Med . 2023 Oct; 12(20). PMID: 37892706
Background: Normothermic ex situ perfusion of vascularized composite allografts (VCAs) necessitates high oxygen demand and, thus, increased metabolic activity, which, in turn, requires the use of blood-based perfusion solutions. However,...
9.
Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal Kidney
Schierbaum L, Schneider S, Buerger F, Halawi A, Seltzsam S, Wang C, et al.
Nephron . 2023 Jul; 147(11):685-692. PMID: 37499630
Introduction: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney disease in the first 3 decades of life. Over 40 genes have...
10.
Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of life
Elshafey S, Thabet M, Elwafa R, Schneider R, Shril S, Buerger F, et al.
Acta Paediatr . 2023 Feb; 112(6):1324-1332. PMID: 36847718
Aim: The earlier the onset of proteinuria, the higher the incidence of genetic forms. Therefore, we aimed to analyse the spectrum of monogenic proteinuria in Egyptian children presenting at age...