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Thomas Haaf (1959-)

Arzt

Name	Thomas Haaf
Time	1959- (Date of birth and death)
Place	Würzburg (Wirkungsort) Regierungsbezirk Unterfranken (Geburtsort) Deutschland
Gender	männlich
Academic degree	Prof. Dr. med.
Profession	Arzt (characteristic profession) Hochschullehrer
Related	Julius-Maximilians-Universität Würzburg Medizin (Studienfach)
Further information	Professor am Institut für Humangenetik der Universität Würzburg
Source	Vorlage, WWW: http://www.humgen.biozentrum.uni-wuerzburg.de/forschung/ag_prof_haaf/ (Stand: 13.03.2017)
Record type	Person
GND-Identifier	1099337496
Record ID	1099337496
Involved in show all Whole-genome sequencing, as a powerful diagnostic tool in hearing loss, reveals novel variants in PTPRQ missed by whole-exome sequencing A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation Age‐related and species‐specific methylation changes in the protein‐coding marmoset sperm epigenome D4Z4 hypomethylation in human germ cells Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome A genome-wide transcriptomic analysis of embryos fathered by obese males in a murine model of diet-induced obesity Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss Genetic and epigenetic changes in clonal descendants of irradiated human fibroblasts Identifizierung und Charakterisierung neuer, mit Hörstörungen assoziierter Gene und Varianten mittels Exom-Sequenzierung Lipid droplets in mammalian eggs are utilized during embryonic diapause Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity Evolution of the degenerated Y-chromosome of the swamp guppy, Micropoecilia picta Genetic characterization of rat hepatic stellate cell line HSC-T6 for in vitro cell line authentication Genetic characterization of rat hepatic stellate cell line PAV-1 Neuroepigenomics in Alzheimer’s disease: The single cell ADds Novel loss-of-function variants in CDC14A are associated with recessive sensorineural hearing loss in Iranian and Pakistani patients Rat hepatic stellate cell line CFSC-2G: genetic markers and short tandem repeat profile useful for cell line authentication Species-specific paternal age effects and sperm methylation levels of developmentally important genes Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line Authentication Rat Hepatic Stellate Cell Line CFSC-2G: Genetic Markers and Short Tandem Repeat Profile Useful for Cell Line Authentication Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans Disease Manifestation and Inflammatory Activity as Modulators of Th17/Treg Balance and RORC/FoxP3 Methylation in Systemic Sclerosis Epigenetic changes in preimplantation embryos from a diabetic pregnancies Epigenetic dysregulation in the developing Down syndrome cortex Epigenetic Information from Ancient DNA Provides New Insights into Human Evolution : Commentary on Gokhman D et al. (2014): Reconstructing the DNA Methylation Maps of the Neanderthal and the Denisovan. Science 344:523–527 Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families Genome‐wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between cytosine‐phosphate‐guanine methylation and histological subtypes Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes Erweiterung des genetischen Mutationsspektrums verschiedener Krankheitsbilder und Identifizierung neuer krankheitsrelevanter Gene im Menschen mittels Whole Exome Sequenzierung Hypermethylation of FOXP3 Promoter and Premature Aging of the Immune System in Female Patients with Panic Disorder? Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer’s disease-related dysregulation Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiation Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3 Genetics of Tinnitus: Still in its Infancy Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals Expanding the clinical phenotype of IARS2-related mitochondrial disease MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss Hereditary hearing loss SNP-microarray pilot study The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management The Arboranan Frogs: Introduction Altersassoziierte und strahleninduzierte Veränderungen des genomweiten DNA-Methylierungs-Profils Analyse genetischer Stabilität in den Nachkommen bestrahlter Zellen mittels klassischer Chromosomenbänderung und verschiedener Hochdurchsatz-Techniken Expanding the clinical phenotype of IARS2-related mitochondrial disease Prenatal and postnatal experiences associated with epigenetic changes in the adult mouse brain Epigenetic signatures of gestational diabetes mellitus on cord blood methylation Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family Alterungsbedingte Effekte auf DNA-Methylierungsprofile entwicklungsrelevanter Gene in Eizellen und Embryonen am Modellorganismus Bos taurus Zu Grad, Konfiguration und Verlauf der Schallempfindungsschwerhörigkeit bei Kindern mit einer Connexin-26-Mutation Epigenetics of gestational diabetes mellitus and offspring health: the time for action is in early stages of life Molecular Characterization of Genes Involved in Hearing Loss

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Katalog der Deutschen Nationalbibliothek

Thomas Haaf (1959-)

Whole-genome sequencing, as a powerful diagnostic tool in hearing loss, reveals novel variants in PTPRQ missed by whole-exome sequencing

A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation

Age‐related and species‐specific methylation changes in the protein‐coding marmoset sperm epigenome

D4Z4 hypomethylation in human germ cells

Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome

A genome-wide transcriptomic analysis of embryos fathered by obese males in a murine model of diet-induced obesity

Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss

Genetic and epigenetic changes in clonal descendants of irradiated human fibroblasts

Identifizierung und Charakterisierung neuer, mit Hörstörungen assoziierter Gene und Varianten mittels Exom-Sequenzierung

Lipid droplets in mammalian eggs are utilized during embryonic diapause

Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity

Evolution of the degenerated Y-chromosome of the swamp guppy, Micropoecilia picta

Genetic characterization of rat hepatic stellate cell line HSC-T6 for in vitro cell line authentication

Genetic characterization of rat hepatic stellate cell line PAV-1

Neuroepigenomics in Alzheimer’s disease: The single cell ADds

Novel loss-of-function variants in CDC14A are associated with recessive sensorineural hearing loss in Iranian and Pakistani patients

Rat hepatic stellate cell line CFSC-2G: genetic markers and short tandem repeat profile useful for cell line authentication

Species-specific paternal age effects and sperm methylation levels of developmentally important genes

Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line Authentication

Rat Hepatic Stellate Cell Line CFSC-2G: Genetic Markers and Short Tandem Repeat Profile Useful for Cell Line Authentication

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment

Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Disease Manifestation and Inflammatory Activity as Modulators of Th17/Treg Balance and RORC/FoxP3 Methylation in Systemic Sclerosis

Epigenetic changes in preimplantation embryos from a diabetic pregnancies

Epigenetic dysregulation in the developing Down syndrome cortex

Epigenetic Information from Ancient DNA Provides New Insights into Human Evolution : Commentary on Gokhman D et al. (2014): Reconstructing the DNA Methylation Maps of the Neanderthal and the Denisovan. Science 344:523–527

Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families

Genome‐wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between cytosine‐phosphate‐guanine methylation and histological subtypes

Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements

Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients

CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development

Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes

Erweiterung des genetischen Mutationsspektrums verschiedener Krankheitsbilder und Identifizierung neuer krankheitsrelevanter Gene im Menschen mittels Whole Exome Sequenzierung

Hypermethylation of FOXP3 Promoter and Premature Aging of the Immune System in Female Patients with Panic Disorder?

Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer’s disease-related dysregulation

Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report

Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiation

Generation of a human induced pluripotent stem cell (iPSC) line from a 51-year-old female with attention-deficit/hyperactivity disorder (ADHD) carrying a duplication of SLC2A3

Genetics of Tinnitus: Still in its Infancy

Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals

Expanding the clinical phenotype of IARS2-related mitochondrial disease

MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss

Hereditary hearing loss SNP-microarray pilot study

The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian family

Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management

The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management

The Arboranan Frogs: Introduction

Altersassoziierte und strahleninduzierte Veränderungen des genomweiten DNA-Methylierungs-Profils

Analyse genetischer Stabilität in den Nachkommen bestrahlter Zellen mittels klassischer Chromosomenbänderung und verschiedener Hochdurchsatz-Techniken

Expanding the clinical phenotype of IARS2-related mitochondrial disease

Prenatal and postnatal experiences associated with epigenetic changes in the adult mouse brain

Epigenetic signatures of gestational diabetes mellitus on cord blood methylation

Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family

Alterungsbedingte Effekte auf DNA-Methylierungsprofile entwicklungsrelevanter Gene in Eizellen und Embryonen am Modellorganismus Bos taurus

Zu Grad, Konfiguration und Verlauf der Schallempfindungsschwerhörigkeit bei Kindern mit einer Connexin-26-Mutation

Epigenetics of gestational diabetes mellitus and offspring health: the time for action is in early stages of life

Molecular Characterization of Genes Involved in Hearing Loss