Jens Michael Hertz - Concepedia

Author

Jens Michael Hertz

Also Known As

Hans Gjørup, Hertz, Jens Michael, J HERTZ, J Hertz, J M Hertz, J. M. Hertz, J.M. Hertz, JENS M. HERTZ, JENS MICHAEL HERTZ, JM Hertz

185

Publications

5.6K

Citations

H-Index

154

Concepts

All Affiliations

Aarhus University Hospital Odense University Hospital Aarhus University Rigshospitalet University of Copenhagen

About

Jens Michael Hertz is an author at Aarhus University Hospital specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	48	2.3K
2	Public Health	10	10	500
3	Health Sciences	2	2	188
4	Natural Sciences	2	2	34
5	Engineering	1	1	139

Jens Michael Hertz

Publications

5.1K

Citations

H-Index

Page 1

	Year	Citations
X-linked Alport Syndrome Jean Philippe Jaïs, Bertrand Knebelmann, Iannis Giatras, Journal of the American Society of Nephrology	2000	574
X-Linked Alport Syndrome Jean Philippe Jaïs, Bertrand Knebelmann, Iannis Giatras, Journal of the American Society of Nephrology	2003	469
Transcriptional regulator PRDM12 is essential for human pain perception Ya-Chun Chen, Michaela Auer‐Grumbach, Shinya Matsukawa, Nature Genetics Pain SyndromeSignal TransductionHealth SciencesPain MedicineMolecular Pain	2015	170
Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2 Erik‐Jan Kamsteeg, Claudio Catalli, Jens Michael Hertz, European Journal of Human Genetics Molecular DiagnosisGeneticsDiagnosisPathologyMendelian Disorder	2012	160
Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient. Jingbin Zhou, Jens Michael Hertz, Anu Leinonen, Journal of Biological Chemistry Female CousinFibrosisMendelian DisorderCollagen ChainGenetic Disorder	1992	148
High mutation detection rate in the COL4A5 collagen gene in suspected Alport syndrome using PCR and direct DNA sequencing. Paula Martin, Niina Heiskari, Jing Zhou, Journal of the American Society of Nephrology EngineeringGeneticsGenetic EpidemiologyPathologyMolecular Genetics	1998	139
Anthropometry in Klinefelter Syndrome - Multifactorial Influences Due to CAG Length, Testosterone Treatment and Possibly Intrauterine Hypogonadism Simon Chang, Anne Skakkebæk, Christian Trolle, The Journal of Clinical Endocrinology & Metabolism	2014	134
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism Georgia Karadima, Merete Bugge, Peter Nicolaidis, European Journal of Human Genetics Developmental BiologyCytogeneticsGenetic DisorderGeneticsTrisomy 8	1998	131
Non-disjunction of chromosome 13 Merete Bugge, Andrew Collins, Jens Michael Hertz, Human Molecular Genetics CytogeneticsGeneticsMolecular GeneticsParental OriginReproductive Biology	2007	118
Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria Judy Savige, Helen Storey, E. Watson, European Journal of Human Genetics	2021	117

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