Ahmet Yaramış

A Randomized Trial of Granulocyte-Macrophage Colony-Stimulating Factor in Neonates With Sepsis and Neutropenia

Kemal Bi ̇lgi ̇n, Ahmet Yaramış, Kenan Haspolat et al. · PEDIATRICS · 2001 · 138 citations

Medicine, Hematology, Pediatrics +17

Identification of mutations in the<i>MYO9A</i>gene in patients with congenital myasthenic syndrome

Emily O’Connor, Ana Töpf, Juliane S. Müller et al. · Brain · 2016 · 57 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing

Daliya Kancheva, Derek Atkinson, Peter De Rijk et al. · Genetics in Medicine · 2015 · 39 citations · Full text

Life Sciences, Genetics, Neurology +17

Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

Leslie Matalonga, Steven Laurie, Anastasios Papakonstantinou et al. · Journal of Molecular Diagnostics · 2020 · 34 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases

Semra Hız Kurul, Yavuz Oktay, Ana Töpf et al. · Brain · 2021 · 34 citations · Full text

Life Sciences, Genetics, Pediatrics +13