Esra Battaloğlu

Q: What Schools Are Affiliated With Esra Battaloğlu

Esra Battaloğlu is affiliated with the following schools: Koç University, Middle East Technical University, Bilkent University, Boğaziçi University, Sabancı University

Esra Battaloğlu's AcademicInfluence.com Rankings

Esra Battaloğlu

Biology

#6609

World Rank

#9361

Historical Rank

Genetics

#1437

World Rank

#1539

Historical Rank

Molecular Biology

#1845

World Rank

#1874

Historical Rank

biology Degrees

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Biology

Esra Battaloğlu's Degrees

Bachelors Molecular Biology and Genetics Middle East Technical University
Masters Molecular Biology and Genetics Middle East Technical University
PhD Molecular Biology and Genetics Bilkent University

Why Is Esra Battaloğlu Influential?

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According to Wikipedia, Esra Battaloğlu is a Turkish geneticist researching the human genetics of inherited peripheral neuropathies. She is an assistant professor at Boğaziçi University. Education Battaloğlu graduated from High School TED Ankara Koleji in 1982. She completed a B.S. in the department of biology at the Middle East Technical University in 1986. Battaloğlu earned an M.S. and Ph.D. in the department of biology at Boğaziçi University.

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Esra Battaloğlu's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Voltage-Gated Sodium Channel Expression and Potentiation of Human Breast Cancer Metastasis (2005) (422)
A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases (2014) (297)
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy. (2015) (206)
Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy. (2003) (186)
Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. (2007) (134)
Genetic spectrum of hereditary neuropathies with onset in the first year of life (2011) (104)
A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis. (2006) (73)
Clinicopathological and genetic study of early-onset demyelinating neuropathy. (2004) (72)
Motor protein mutations cause a new form of hereditary spastic paraplegia (2014) (47)
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 (2015) (35)
Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients (2000) (34)
Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D (2013) (33)
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach (2014) (31)
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia (2017) (29)
Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians (2000) (24)
MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability (2017) (23)
Neonatal Nav1.5 protein expression in normal adult human tissues and breast cancer. (2017) (22)
Low dose vincristine-induced severe polyneuropathy in a Hodgkin lymphoma patient: a case report (vincristine-induced severe polyneuropathy). (2009) (21)
SIK2 attenuates proliferation and survival of breast cancer cells with simultaneous perturbation of MAPK and PI3K/Akt pathways (2018) (20)
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene (2004) (19)
Charcot‐Marie‐Tooth disease associated with Type 2 diabetes mellitus (2001) (17)
A multicenter retrospective study of charcot‐marie‐tooth disease type 4B (CMT4B) associated with mutations in myotubularin‐related proteins (MTMRs) (2019) (17)
Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: A case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decade (2009) (16)
Ultrasonographic findings in hereditary neuropathy with liability to pressure palsies (2015) (16)
Clinical and genetic features of PKAN patients in a tertiary centre in Turkey (2017) (16)
X-linked Charcot-Marie-Tooth disease and multiple sclerosis (2007) (15)
Nerve conduction studies in Charcot–Marie–Tooth disease in a cohort from Turkey (2011) (13)
High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus–Merzbacher disease (2013) (11)
DNA analysis in Turkish Duchenne/Becker muscular dystrophy families (1992) (11)
A LARGE FAMILY WITH CHARCOT-MARIE-TOOTH TYPE 1A AND TYPE 2 DIABETES MELLITUS (2006) (11)
Combination of myotonic dystrophy and hereditary motor and sensory neuropathy (2010) (11)
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype (2019) (9)
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family (2019) (9)
Two novel mutations in the MPZ gene coding region in Charcot‐Marie‐Tooth type 1 patients of Turkish origin: S54P, [I30del; GVYI29ins] (1999) (5)
Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages (2022) (4)
Recessively transmitted predominantly motor neuropathies. (2013) (4)
A multiplexed ARMS-PCR approach for the detection of common MECP2 mutations. (2009) (3)
MCM 3 AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability (3)
Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity. (2022) (3)
Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort (2021) (2)
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family (2019) (2)
Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder (2021) (1)
Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey. (2020) (1)
Warfarin maintenance dose associated with genetic polymorphisms of CYP2C9. (2017) (1)
An autosomal recessive CMT family with a new mutation in the NDRG1 gene (2013) (0)
A Multiplexed ARMS-PCR Approach for the Detection of CommonMECP2Mutations (2009) (0)
Reply (2012) (0)
Genotype-phenotype Correlation in Pelizaeus Merzbacher Disease and Pelizaeus Merzbacher-like Disease (2018) (0)
MCM3AP in recessive axonal neuropathy and mild intellectual disability (2018) (0)
Congenital Hypothyroidism But Not Athyreosis A Novel Missense Mutation in Human TTF-2 ( FKHL 15 ) Gene Associated with Society (2006) (0)
Herediter Spastik Paraparezi: Genetikten Patogeneze (2011) (0)
Selective Bilateral Vestibular Neuropathy in a Turkish CMT1B Family With a Novel MPZ Mutation (2020) (0)
The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype (2019) (0)
Genotype-Phenotype Correlation in Pelizaeus Merzbacher Disease and Pelizaeus Merzbacher-Like Disease Running Head : Genotype-Phenotype in Pelizaeus Merzbacher (2018) (0)
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach (2014) (0)
Clinical and Genetic Heterogeneity in Charcot-Marie-Tooth Neuropathy Type 2 Patients from Turkey (P5.024) (2016) (0)
Carrier detection by DNA analysis in Duchenne muscular dystrophy families. (1992) (0)
Genotypic And Phenotypic Features of Patients with GJB1 Mutations: Single Center Experience (P11-8.003) (2023) (0)
A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotonia. (2023) (0)
Detection of junction fragments in Turkish CMT1A/HNPP patients (1998) (0)
Congenital Hypothyroidism But Not Athyreosis A Novel Missense Mutation in Human TTF-2 (FKHL15) Gene Associated with (2006) (0)
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features (2021) (0)
ERRATUM: Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D (2014) (0)
A Family with Vocal Cord Paralysis Associated with GDAP1 Mutation in Giresun, Turkey (2015) (0)
G.P.1.10 Clinicopathological and genetic study of CMT2 (2008) (0)

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Other Resources About Esra Battaloğlu

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What Schools Are Affiliated With Esra Battaloğlu?

Esra Battaloğlu is affiliated with the following schools:

Esra Battaloğlu's Academic­Influence.com Rankings

Esra Battaloğlu's Degrees

Why Is Esra Battaloğlu Influential?

Esra Battaloğlu's Published Works

Published Works

Other Resources About Esra Battaloğlu

What Schools Are Affiliated With Esra Battaloğlu?

Esra Battaloğlu's AcademicInfluence.com Rankings