Suchergebnisse - "Fuhrmann, Nico"

PubPharm (19)

1

Polygenic adaptation from standing genetic variation allows rapid ecotype formation

enthalten in: bioRxiv.org | 2024

von Fuhrmann, N. | Prakash, C. | Kaiser, T.

2

Polygenic adaptation from standing genetic variation allows rapid ecotype formation

enthalten in: eLife | 2023

von Fuhrmann, N. | Prakash, C. | Kaiser, T.

3

Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease

enthalten in: Human mutation | 2021

von Keller, N. | Paketci, C. | Altmueller, J. | +14

4

The importance of DNA barcode choice in biogeographic analyses - a case study on marine midges of the genus Clunio

enthalten in: Genome | 2021

von Fuhrmann, N. | Kaiser, T.

5

Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease

enthalten in: Human mutation | 2021

von Keller, N. | Paketci, C. | Altmueller, J. | +14

6

De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation

enthalten in: American journal of human genetics | 2020

von Mendoza-Ferreira, N. | Karakaya, M. | Cengiz, N. | +18

7

A Dipteran's Novel Sucker Punch : Evolution of Arthropod Atypical Venom with a Neurotoxic Component in Robber Flies (Asilidae, Diptera)

enthalten in: Toxins | 2018

von Drukewitz, S. | Fuhrmann, N. | Undheim, E. | +6

8

Dominant optic atrophy, OPA1, and mitochondrial quality control : understanding mitochondrial network dynamics

enthalten in: Molecular neurodegeneration | 2013

von Alavi, M. | Fuhrmann, N.

9

Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamics

enthalten in: Molecular neurodegeneration | 2013

von Alavi, M. | Fuhrmann, N.

10

A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16

enthalten in: Human molecular genetics | 2011

von Carelli, V. | Schimpf, S. | Fuhrmann, N. | +22