Pia Hermanns - Concepedia

Concepedia

Author

Pia Hermanns

Johannes Gutenberg University Mainz

Also Known As

Hermanns P, Hermanns, P., Hermanns, Pia, P Hermanns, P M Hermanns, P. Hermanns, Pia Hermanns

63

Publications

1.4K

Citations

22

H-Index

53

Concepts

All Affiliations

Johannes Gutenberg University Mainz Baylor College of Medicine University Medical Center of the Johannes Gutenberg University Mainz Howard Hughes Medical Institute University of Freiburg

PH

About

Pia Hermanns is an author at Johannes Gutenberg University Mainz specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	568
2	Natural Sciences	3	3	191
3	Cell Biology	3	3	230
4	Anatomy	1	1	24
5	Biochemistry	1	1	54

Pia Hermanns

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32

Publications

1.4K

Citations

22

H-Index

	Year	Citations
Effectiveness of hand and rotary instrumentation for removing a new synthetic polymer‐based root canal obturation material (Epiphany) during retreatment Jörg Schirrmeister, K. M. Meyer, Pia Hermanns, International Endodontic Journal	2006	119
TBX15 Mutations Cause Craniofacial Dysmorphism, Hypoplasia of Scapula and Pelvis, and Short Stature in Cousin Syndrome Ekkehart Lausch, Pia Hermanns, Henner F. Farin, The American Journal of Human Genetics Cousin SyndromeShort StatureGenetic DisorderGeneticsCraniofacial Anomalies	2008	110
Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia Pia Hermanns, Alison A. Bertuch, Terry Bertin, Human Molecular Genetics GeneticsMolecular BiologyPathologyMolecular GeneticsDisease Gene Identification	2005	110
Congenital Joint Dislocations Caused by Carbohydrate Sulfotransferase 3 Deficiency in Recessive Larsen Syndrome and Humero-Spinal Dysostosis Pia Hermanns, Sheila Unger, Antonio Rossi, The American Journal of Human Genetics Carbohydrate Sulfotransferase 3Recessive Larsen SyndromeOrthopaedic SurgeryCongenital Joint Dislocations	2008	102
A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations Andreas Herzog, Ralf Hartung, Arnold Reuser, Orphanet Journal of Rare Diseases	2012	88
Detectability of residual Epiphany and gutta‐percha after root canal retreatment using a dental operating microscope and radiographs – an <i>ex vivo</i> study Jörg Schirrmeister, Pia Hermanns, K. M. Meyer, International Endodontic Journal	2006	82
Brachy–syndactyly caused by loss of <i>Sfrp2</i> function Roy Morello, Terry Bertin, Silke Schlaubitz, Journal of Cellular Physiology Transcriptional RegulationDevelopmental BiologyTissue DevelopmentConsistent ShorteningSfrp2 Results	2008	66
<i>RMRP</i> mutations in cartilage‐hair hypoplasia Pia Hermanns, Alyssa A. Tran, Elda Munivez, American Journal of Medical Genetics Part A	2006	64
A Single Copy of the Recently Identified Dual Oxidase Maturation Factor (DUOXA) 1 Gene Produces Only Mild Transient Hypothyroidism in a Patient with a Novel Biallelic DUOXA2 Mutation and Monoallelic DUOXA1 Deletion Imge Hulur, Pia Hermanns, C Nestoris, The Journal of Clinical Endocrinology & Metabolism	2011	60
Expression profile of <i>Papss2</i> (3′‐phosphoadenosine 5′‐phosphosulfate synthase 2) during cartilage formation and skeletal development in the mouse embryo Christiane Stelzer, Annette Brimmer, Pia Hermanns, Developmental Dynamics GlycobiologyMolecular BiologyExpression ProfileBiosynthesisTissue Development	2007	54

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