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Pia Hermanns | Researcher profile | ResearchHub

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Pia Hermanns

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Researcher profile

Pia Hermanns

ResearchHub researcher

Johannes Gutenberg University Mainz

2

Publications

0

Citations

0

H-index

0

Recent H-index

2

Reads

0

Followers

Overview Research Publications Projects Datasets Questions Impact Network Activity

Overview

Research identity

Research areas

Not available

Education

Not available

Research

Research outputs

Public works are drawn from admitted ResearchHub scholarly records.

Publications

Selected public works

Search public worksYearWork typeSort works

2 of 2 listed works

Exports contain available public metadata for the works currently shown.

Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders

Molecular and Cellular Pediatrics · 2015 · journal-article

0 citations · 0 reads

A novel mutation in the PAX8 promoter region causes permanent congenital hypothyroidism in a patient with Down’s Syndrome

Molecular and Cellular Pediatrics · 2014 · journal-article

0 citations · 2 reads

Projects

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No public projects are available.

Datasets

Public datasets

No public datasets are available.

Questions

Questions & answers

Not available

Impact

Measured impact

Publications: 2
Citations: 0
H-index: 0
Recent H-index: 0
Reads: 2

H-index follows the standard Hirsch definition: the largest h for which h publications each have at least h citations. Recent H-index applies the same calculation to the five most recent complete calendar years (2021-2025); the current year is excluded while incomplete.

Affiliations

Institutions

JJohannes Gutenberg University MainzAffiliation

Identifiers

Scholarly links

Not available

Network

Research network

0 followers

Public network totals only

Activity

Recent activity

Not available

Recognition

Professional record

Not available