# Davut Pehli̇van

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/davut-pehlivan/

## Facts

| Field | Value |
| --- | --- |
| Citations | 6,698 |
| Field | Genomics and Rare Diseases |
| h-index | 38 |
| i10-index | 106 |
| Last Known Institution | Baylor College of Medicine |
| OpenAlex ID | https://openalex.org/A5023261072 |
| ORCID iD | 0000-0001-5788-0270 |
| Works | 189 |

## Researcher papers

- [Detection of mosaic and population-level structural variants with Sniffles2](https://scholariq.org/papers/detection-of-mosaic-and-population-level-structural-variants-with-sniffles2/)
- [A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases](https://scholariq.org/papers/a-drosophila-genetic-resource-of-mutants-to-study-mechanisms-underlying-human/)
- [Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease](https://scholariq.org/papers/genes-that-affect-brain-structure-and-function-identified-by-rare-variant/)
- [Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy](https://scholariq.org/papers/exome-sequence-analysis-suggests-that-genetic-burden-contributes-to-phenotypic/)
- [Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome](https://scholariq.org/papers/inverted-genomic-segments-and-complex-triplication-rearrangements-are-mediated/)
- [Human CLP1 Mutations Alter tRNA Biogenesis, Affecting Both Peripheral and Central Nervous System Function](https://scholariq.org/papers/human-clp1-mutations-alter-trna-biogenesis-affecting-both-peripheral-and-central/)
- [Insights into genetics, human biology and disease gleaned from family based genomic studies](https://scholariq.org/papers/insights-into-genetics-human-biology-and-disease-gleaned-from-family-based/)
- [Compound Heterozygosity for Loss-of-Function Lysyl-tRNA Synthetase Mutations in a Patient with Peripheral Neuropathy](https://scholariq.org/papers/compound-heterozygosity-for-loss-of-function-lysyl-trna-synthetase-mutations-in/)
- [ARMC4 Mutations Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry](https://scholariq.org/papers/armc4-mutations-cause-primary-ciliary-dyskinesia-with-randomization-of-left/)
- [Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes](https://scholariq.org/papers/global-transcriptional-disturbances-underlie-cornelia-de-lange-syndrome-and/)
- [Assessing the Burden on Caregivers of MECP2 Duplication Syndrome](https://scholariq.org/papers/assessing-the-burden-on-caregivers-of-mecp2-duplication-syndrome/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)

## Researcher university

- [Baylor College of Medicine](https://scholariq.org/institutions/baylor-college-of-medicine/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.