Hanns-Georg Klein

Hanns-Georg Klein

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Hanns-Georg Klein

Hanns-Georg Klein

Publications by authors named "Hanns-Georg Klein"

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18Publications

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Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providers.

Eur J Med Genet 2020 Jan 14;63(1):103616. Epub 2019 Jan 14.

Prenatal Genetic Diagnosis Unit, Genetic Institute, Tel Aviv Medical Center, Tel Aviv, Israel. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S17697212183071
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http://dx.doi.org/10.1016/j.ejmg.2019.01.006DOI Listing
January 2020

Variant panorama in 1,385 index patients and sensitivity of expanded next-generation sequencing panels in arrhythmogenic disorders.

Cardiovasc Diagn Ther 2019 Oct;9(Suppl 2):S292-S298

Center for Human Genetics and Laboratory Diagnostics, Martinsried, Germany.

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http://dx.doi.org/10.21037/cdt.2019.06.06DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837920PMC
October 2019

Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis.

Pediatr Nephrol 2018 03 6;33(3):433-437. Epub 2017 Oct 6.

Institute of Human Genetics, Technical University of Munich, Munich, Germany.

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http://dx.doi.org/10.1007/s00467-017-3811-4DOI Listing
March 2018

Lessons From the EThIGII Trial: Proper Putative Benefit Assessment of Low-Molecular-Weight Heparin Treatment in M2/ANXA5 Haplotype Carriers.

Clin Appl Thromb Hemost 2017 Jan 14;23(1):27-33. Epub 2016 Jul 14.

Division of Gynecological Endocrinology and Reproductive Medicine, Department of Gynecology and Obstetrics, Klinikum der Ludwig-Maximilians-Universität, Munich, Germany.

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http://dx.doi.org/10.1177/1076029616658117DOI Listing
January 2017

Rare co-occurrence of osteogenesis imperfecta type I and autosomal dominant polycystic kidney disease.

World J Pediatr 2016 Nov 8;12(4):501-503. Epub 2016 Apr 8.

Department of Pediatrics, General Hospital, Celle, Germany.

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http://dx.doi.org/10.1007/s12519-016-0014-1DOI Listing
November 2016

Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.

Pediatr Nephrol 2016 Jun 25;31(6):941-55. Epub 2016 Jan 25.

Center for Human Genetics and Laboratory Diagnostics Dr. Klein, Dr. Rost and Colleagues, Martinsried, Germany.

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http://dx.doi.org/10.1007/s00467-015-3302-4DOI Listing
June 2016

Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndrome.

Gene 2013 Sep 31;526(2):474-7. Epub 2013 May 31.

Center for Human Genetics and Laboratory Medicine Dr. Klein, Dr. Rost and Colleagues, Martinsried, Germany.

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http://dx.doi.org/10.1016/j.gene.2013.05.045DOI Listing
September 2013

A novel interstitial deletion of 10q24.2q24.32 in a patient with renal coloboma syndrome.

Eur J Med Genet 2012 Mar 31;55(3):211-5. Epub 2012 Jan 31.

Center for Human Genetics and Laboratory Medicine Dr. Klein and Dr. Rost, Martinsried, Germany.

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http://dx.doi.org/10.1016/j.ejmg.2012.01.011DOI Listing
March 2012

Novel PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease (ADPKD).

Nephrol Dial Transplant 2011 Jul 29;26(7):2181-8. Epub 2010 Nov 29.

Center for Human Genetics and Laboratory Medicine Dr Klein and Dr Rost, Martinsried, Germany.

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http://dx.doi.org/10.1093/ndt/gfq720DOI Listing
July 2011

Left ventricular non-compaction associated with a genetic variant of the CYP2C9 gene.

Heart Lung Circ 2006 Aug 3;15(4):269-71. Epub 2006 Apr 3.

Department of Cardiothoracic Surgery, Julius-Maximilians University of Wuerzburg, Oberduerrbacherstr. 7, 97080 Wuerzburg, Germany.

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http://linkinghub.elsevier.com/retrieve/pii/S144395060600043
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http://dx.doi.org/10.1016/j.hlc.2006.02.007DOI Listing
August 2006