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Çiğdem Köroğlu

5PUBLICATIONS

9CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Anthropological geneticsGene expression (incl. microarray and other genome-wide approaches)Genome structure and regulationNeurology and neuromuscular diseases

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Publications (5)

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|Aug 28, 2024

Identification and functional validation of rare coding variants in genes linked to monogenic obesity.

Çiğdem Köroğlu, Michael Traurig, Yunhua L Muller

|Aug 27, 2024

De Novo Genome Assemblies From Two Indigenous Americans from Arizona Identify New Polymorphisms in Non-Reference Sequences.

Çiğdem Köroğlu, Peng Chen, Michael Traurig

|Jan 19, 2022

Functional variants in cytochrome b5 type A (CYB5A) are enriched in Southwest American Indian individuals and associate with obesity.

Samantha E Day, Michael Traurig, Pankaj Kumar

|Feb 22, 2021

Exome Sequencing of 21 Bardet-Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians.

Samantha E Day, Yunhua L Muller, Cigdem Koroglu

|Nov 01, 2017

GNE missense mutation in recessive familial amyotrophic lateral sclerosis.

Çiğdem Köroğlu, Rezzak Yılmaz, Mine Hayriye Sorgun

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Frequent Collaborators

3 joint publications

Samantha E Day

3 joint publications

Clifton Bogardus

2 joint publications

Paolo Piaggi

1 joint publications

Yunhua L Muller

1 joint publications

Peng Chen

1 joint publications

Michael Traurig

1 joint publications

Serdar Altok

1 joint publications

Leslie J Baier

1 joint publications

Cristopher V Van Hout

Frequent Collaborators

3 joint publications

Samantha E Day

3 joint publications

Clifton Bogardus

2 joint publications

Paolo Piaggi

1 joint publications

Yunhua L Muller

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