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John Schulga | ORCID 0000-0001-9688-1997 | ResearchHub

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John Schulga

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Researcher profile

John Schulga

ResearchHub researcher

1

Publications

0

Citations

0

H-index

0

Recent H-index

3

Reads

0

Followers

Overview Research Publications Projects Datasets Questions Impact Network Activity

Overview

Research identity

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Research

Research outputs

Public works are drawn from admitted ResearchHub scholarly records.

Publications

Selected public works

Search public worksYearWork typeSort works

1 of 1 listed works

Exports contain available public metadata for the works currently shown.

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 · 3 reads

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Impact

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Publications: 1
Citations: 0
H-index: 0
Recent H-index: 0
Reads: 3

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.

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ORCID: 0000-0001-9688-1997

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0 followers

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