Andreas Zankl - Concepedia

Author

Andreas Zankl

The University of Queensland ORCID

Also Known As

A Zankl, A. McInerney-Leo, A. Zankl, ANDREAS ZANKL, Andreas Zankl, Zankl, Andreas, Zankl, Andreas;

132

Publications

5.6K

Citations

H-Index

Concepts

All Affiliations

The University of Queensland Royal Brisbane and Women's Hospital The University of Sydney Royal Children's Hospital Children's Hospital at Westmead

About

Andreas Zankl is an author at The University of Queensland specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	22	1.5K
2	Public Health	6	6	735
3	Engineering	3	3	52
4	Biostatistics	3	3	52
5	Cell Biology	3	3	206

Andreas Zankl

Publications

4.2K

Citations

H-Index

Page 1

	Year	Citations
Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome Gillian Rice, Teresa Patrick, Rekha Parmar, The American Journal of Human Genetics CardiomyopathyHeart FailureCardiorenal SyndromesCardiovascular DiseaseMolecular Phenotype	2007	442
The Human Phenotype Ontology in 2024: phenotypes around the world Michael Gargano, Nicolas Matentzoglu, Ben Coleman, Nucleic Acids Research	2023	311
The Zinc Transporter SLC39A13/ZIP13 Is Required for Connective Tissue Development; Its Involvement in BMP/TGF-β Signaling Pathways Toshiyuki Fukada, Natacha Civic, Tatsuya Furuichi, PLoS ONE	2008	287
The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease Tudor Groza, Sebastian Köhler, Dawid Moldenhauer, The American Journal of Human Genetics	2015	239
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans Jan Halbritter, Albane A. Bizet, Miriam Schmidts, The American Journal of Human Genetics	2013	225
Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in <i>PLOD2</i> Russia Hà-Vinh Leuchter, Yasemin Alanay, Ruud A. Bank, American Journal of Medical Genetics Part A	2004	175
Short-Rib Polydactyly and Jeune Syndromes Are Caused by Mutations in WDR60 Aideen McInerney‐Leo, Miriam Schmidts, Claudio R. Cortés, The American Journal of Human Genetics	2013	131
Pseudoachondroplasia and multiple epiphyseal dysplasia: A 7‐year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution Gail C. Jackson, Lauréane Mittaz‐Crettol, Jacqueline Taylor, Human Mutation	2011	125
Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy Miriam Schmidts, Julia Vodopiutz, Sonia Christou-Savina, The American Journal of Human Genetics Genetic DisorderGeneticsDegenerative DiseaseMolecular GeneticsDisease Gene Identification	2013	122
Growth charts for nose length, nasal protrusion, and philtrum length from birth to 97 years Andreas Zankl, Lukas Eberle, Luciano Molinari, American Journal of Medical Genetics	2002	121

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