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Katrin Beyer | ORCID 0000-0001-8905-1514 | ResearchHub

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Katrin Beyer

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Katrin Beyer

ResearchHub researcher

1

Publications

33

Citations

1

H-index

0

Recent H-index

0

Reads

0

Followers

Overview Research Publications Projects Datasets Questions Impact Network Activity

Overview

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Research

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Public works are drawn from admitted ResearchHub scholarly records.

Publications

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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 predicted TM2 domain of the presenilin 2 gene in a Spanish patient with late-onset Alzheimer's disease

Neurogenetics · 1998 · journal-article

33 citations · 0 reads

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Publications: 1
Citations: 33
H-index: 1
Recent H-index: 0
Reads: 0

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: 0000-0001-8905-1514

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0 followers

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