Davut Pehlivan

Davut Pehlivan

Baylor College of Medicine

H-index: 36

North America-United States

Contact Davut Pehlivan

About Davut Pehlivan

Davut Pehlivan, With an exceptional h-index of 36 and a recent h-index of 32 (since 2020), a distinguished researcher at Baylor College of Medicine, specializes in the field of Neurogenetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Detection of mosaic and population-level structural variants with Sniffles2

Corrections & amendments

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders

The impact of the Turkish population variome on the genomic architecture of rare disease traits

Development and validation of parent-reported gastrointestinal health scale in MECP2 duplication syndrome

A Comprehensive Examination of Clinical Characteristics and Determinants of Long-Term Outcomes in Pediatric Cerebral Sinus Venous Thrombosis

RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS

Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders

Davut Pehlivan Information

University	Baylor College of Medicine
Position	Texas children's hospital
Citations(all)	4755
Citations(since 2020)	3165
Cited By	2769
hIndex(all)	36
hIndex(since 2020)	32
i10Index(all)	72
i10Index(since 2020)	64
Email	Access Email
University Profile Page	Baylor College of Medicine
Google Scholar	View Google Scholar Profile

Davut Pehlivan Skills & Research Interests

Neurogenetics

Top articles of Davut Pehlivan

Detection of mosaic and population-level structural variants with Sniffles2

Nature biotechnology

2024/1/2

Medhat Mahmoud

H-Index: 8

Sairam Behera

H-Index: 4

Davut Pehlivan

H-Index: 24

Christos Proukakis

H-Index: 25

Corrections & amendments

2023

Lei Yu

H-Index: 3

Michael Matschiner

H-Index: 20

Mathieu Cusson

H-Index: 16

Marlene Jahnke

H-Index: 10

Claudia Kruschel

H-Index: 11

Masahiro Nakaoka

H-Index: 20

Francesca Rossi

H-Index: 1

Tal Dagan

H-Index: 28

Yves Van De Peer

H-Index: 78

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders

medRxiv

2024

Riccardo Sangermano

H-Index: 9

Zain Dardas

H-Index: 2

Stephanie Efthymiou

H-Index: 14

David Murphy

H-Index: 10

Amir Bahreini

H-Index: 10

Kerby C Oberg

H-Index: 16

Ramy Saad

H-Index: 5

Reza Boostani

H-Index: 22

Davut Pehlivan

H-Index: 24

Kinga Bujakowska

H-Index: 18

Reza Maroofian

H-Index: 16

The impact of the Turkish population variome on the genomic architecture of rare disease traits

Genetics in Medicine Open

2024/1/1

Davut Pehlivan

H-Index: 24

Yavuz Bayram

H-Index: 18

Tomasz Gambin

H-Index: 36

Pengfei Liu

H-Index: 4

Development and validation of parent-reported gastrointestinal health scale in MECP2 duplication syndrome

Orphanet Journal of Rare Diseases

2024/12

Davut Pehlivan

H-Index: 24

A Comprehensive Examination of Clinical Characteristics and Determinants of Long-Term Outcomes in Pediatric Cerebral Sinus Venous Thrombosis

Pediatric Neurology

2024/6/1

Cemal Karakas

H-Index: 2

Davut Pehlivan

H-Index: 24

RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS

medRxiv

2024

Sheraz Khan

H-Index: 12

Reza Maroofian

H-Index: 16

Farid Ullah

H-Index: 4

Kosuke Izumi

H-Index: 15

Laura K Conlin

H-Index: 26

Pengfei Liu

H-Index: 4

Davut Pehlivan

H-Index: 24

Mina Zamani

H-Index: 6

Peter Bauer

H-Index: 15

Faisal Zafar

H-Index: 2

Stephanie Efthymiou

H-Index: 14

Daniel Gossett

H-Index: 17

Shinya Ohta

H-Index: 9

Erica E Davis

H-Index: 40

Jun Liao

H-Index: 10

Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders

BMC Medical Genomics

2024/4/16

Davut Pehlivan

H-Index: 24

Sensory experiences questionnaire unravels differences in sensory profiles between MECP2‐related disorders

Autism Research

2024/4

Davut Pehlivan

H-Index: 24

Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

Brain

2024/4

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for …

Genetics in Medicine

2024/3/21

Yiming Zheng

H-Index: 10

Oguz Kanca

H-Index: 10

Sehime G Temel

H-Index: 10

Yufeng Shen

H-Index: 6

Xueyang Pan

H-Index: 10

Davut Pehlivan

H-Index: 24

HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data

Nucleic Acids Research

2024/2/28

Zain Dardas

H-Index: 2

He Li

H-Index: 6

Davut Pehlivan

H-Index: 24

Tomasz Gambin

H-Index: 36

MECP2-related disorders while gene-based therapies are on the horizon

2024/2/12

Mirjana Maletic-Savatic

H-Index: 22

Davut Pehlivan

H-Index: 24

Generation of five induced pluripotent stem cell lines from patients with MECP2 Duplication Syndrome

Stem Cell Research

2024/2/1

Jennifer Sheppard

H-Index: 3

Aleksandar Bajic

H-Index: 10

Davut Pehlivan

H-Index: 24

Mirjana Maletic-Savatic

H-Index: 22

Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

The American Journal of Human Genetics

2023/8/3

Tianyu Guo

H-Index: 5

Chen Wang

H-Index: 22

Konrad Platzer

H-Index: 12

Davut Pehlivan

H-Index: 24

Exploring gastrointestinal health in MECP2 duplication syndrome

Neurogastroenterology & Motility

2023/8

Davut Pehlivan

H-Index: 24

Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals

Genetics in Medicine

2023/1/1

Reza Maroofian

H-Index: 16

Toru Sengoku

H-Index: 11

Mina Zamani

H-Index: 6

David Murphy

H-Index: 10

Seda Kanmaz

H-Index: 1

Rachel E Goldberg

H-Index: 10

Chong Ae Kim

H-Index: 27

Serhat Guler

H-Index: 8

Yavuz Bayram

H-Index: 18

Davut Pehlivan

H-Index: 24

Hui Yang

H-Index: 6

Mahsa Motavaf

H-Index: 10

Saeid Safari

H-Index: 23

Kazuhiro Ogata

H-Index: 9

Naomichi Matsumoto

H-Index: 56

The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders

Brain

2023/8

Stephanie Efthymiou

H-Index: 14

Shahnaz Ibrahim

H-Index: 2

Walla Al-Hertani

H-Index: 10

Emma Bedoukian

H-Index: 12

Konrad Platzer

H-Index: 12

Felicity Collins

H-Index: 7

Monkol Lek

H-Index: 52

Javad Akhondian

H-Index: 8

Mojtaba Safi

H-Index: 1

Natalia Gomez-Ospina

H-Index: 15

Davut Pehlivan

H-Index: 24

Peter Bauer

H-Index: 15

John Christodoulou

H-Index: 28

Darius Ebrahimi-Fakhari

H-Index: 27

Reza Maroofian

H-Index: 16

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

The American Journal of Human Genetics

2023/6/1

Davut Pehlivan

H-Index: 24

Ying Hu

H-Index: 10

Lynn Pais

H-Index: 6

Brendan Lee

H-Index: 55

Biallelic variants in ADAMTS15 cause a novel form of distal arthrogryposis

Genetics in Medicine

2022/10/1

Davut Pehlivan

H-Index: 24

Björn Fischer-Zirnsak

H-Index: 23

Burak Durmaz

H-Index: 11

Sigmar Stricker

H-Index: 27

Uwe Kornak

H-Index: 32

See List of Professors in Davut Pehlivan University(Baylor College of Medicine)

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