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T. Haaf · SciRah

Researcher profile · Semantic Scholar

T. Haaf

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T. Haaf — researcher profile on SciRah

h-index: 66
Works: 399
Citations: 17K

Most-cited papers

Gene panel testing of 5589 BRCA1/2‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer
J. Hauke, J. Horváth, E. Gross, A. Gehrig +41 more
2018Cancer Medicine172 citations Open access
Semantic Scholar
Human Mutation
M. Parsons, Emma Tudini, Hong-Yan Li, E. Hahnen +89 more
2019154 citations
Semantic Scholar
Epigenetic signatures of gestational diabetes mellitus on cord blood methylation
Larissa Haertle, N. El Hajj, M. Dittrich, Tobias Müller +3 more
2017Clinical Epigenetics107 citations Open access
Semantic Scholar
DNA methylation signatures in cord blood of ICSI children
N. El Hajj, Larissa Haertle, M. Dittrich, S. Denk +4 more
2017Human Reproduction85 citations Open access
Semantic Scholar
Lipid droplets in mammalian eggs are utilized during embryonic diapause
R. Arena, S. Bisogno, Ł. Gąsior, J. Rudnicka +13 more
2021Proceedings of the National Academy of Sciences of the United States of America72 citations Open access
Semantic Scholar
Epigenetic dysregulation of protocadherins in human disease.
N. El Hajj, M. Dittrich, T. Haaf
2017Seminars in Cell and Developmental Biology71 citations Open access
Semantic Scholar
Biallelic TANGO1 mutations cause a novel syndromal disease due to hampered cellular collagen secretion
Caroline Lekszas, O. Foresti, I. Raote, D. Liedtke +7 more
2019bioRxiv66 citations Open access
Semantic Scholar
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling.
Yuh-Charn Lin, M. Niceta, V. Muto, B. Vona +42 more
2020American Journal of Human Genetics60 citations Open access
Semantic Scholar
In Vitro Fertilization Technology and Child Health.
M. von Wolff, T. Haaf
2020Deutsches Ärzteblatt International52 citations Open access
Semantic Scholar
Male obesity effects on sperm and next-generation cord blood DNA methylation
R. Potabattula, M. Dittrich, M. Schorsch, T. Hahn +2 more
2019PLoS ONE52 citations Open access
Semantic Scholar
Parental metabolic syndrome epigenetically reprograms offspring hepatic lipid metabolism in mice.
D. D. De Jesus, K. Orime, D. Kamińska, Tomohiko Kimura +13 more
2020Journal of Clinical Investigation49 citations Open access
Semantic Scholar
Exposure to Gestational Diabetes Mellitus (GDM) Alters DNA Methylation in Placenta and Fetal Cord Blood.
Zain Awamleh, D. Butcher, A. Hanley, R. Retnakaran +4 more
2021Diabetes Research and Clinical Practice48 citations
Semantic Scholar
Genetics of Tinnitus: Still in its Infancy
B. Vona, I. Nanda, W. Shehata-Dieler, T. Haaf
2017Frontiers in Neuroscience48 citations Open access
Semantic Scholar
Cereblon Enhancer Methylation and IMiD Resistance in Multiple Myeloma.
L. Haertle, S. Barrio, U. Munawar, Seung-Bin Han +22 more
2021Blood46 citations Open access
Semantic Scholar
Epigenetic age prediction in semen – marker selection and model development
A. Pisarek, E. Pośpiech, A. Heidegger, C. Xavier +15 more
2021Aging46 citations Open access
Semantic Scholar
Increasing methylation of sperm rDNA and other repetitive elements in the aging male mammalian germline
R. Potabattula, F. Zacchini, G. Ptak, M. Dittrich +9 more
2020Aging Cell39 citations Open access
Semantic Scholar
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management
L. Tranebjærg, N. Strenzke, Sture Lindholm, N. D. Rendtorff +27 more
2018Human Genetics36 citations Open access
Semantic Scholar
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes
Anna Maierhofer, Julia Flunkert, J. Oshima, G. Martin +5 more
2019Aging Cell35 citations Open access
Semantic Scholar
Gene expression and epigenetic aberrations in F1‐placentas fathered by obese males
M. Mitchell, R. Strick, P. Strissel, R. Dittrich +6 more
2017Molecular Reproduction and Development33 citations Open access
Semantic Scholar
DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome
Yosra Bejaoui, Aleem Razzaq, N. Yousri, J. Oshima +9 more
2022Aging Cell32 citations Open access
Semantic Scholar
SLC2A3 single‐nucleotide polymorphism and duplication influence cognitive processing and population‐specific risk for attention‐deficit/hyperactivity disorder
S. Merker, A. Reif, G. C. Ziegler, H. Weber +20 more
2017Journal of Child Psychology and Psychiatry and Allied Disciplines30 citations Open access
Semantic Scholar
Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing loss
B. Vona, Julia Doll, Michaela A. H. Hofrichter, T. Haaf +1 more
2020Hearing Research28 citations Open access
Semantic Scholar
Age-related methylation changes in the human sperm epigenome
Laura Bernhardt, M. Dittrich, A. Prell, R. Potabattula +6 more
2023Aging27 citations Open access
Semantic Scholar
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish
Sheng-Jia Lin, B. Vona, P. Barbalho, R. Kaiyrzhanov +101 more
2021Genetics in Medicine27 citations Open access
Semantic Scholar
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss
G. Bademci, C. Abad, A. İncesulu, A. Rad +21 more
2018Human Genetics27 citations Open access
Semantic Scholar
Genetic and epigenetic changes in clonal descendants of irradiated human fibroblasts
Julia Flunkert, Anna Maierhofer, M. Dittrich, Tobias Müller +3 more
2018Experimental Cell Research27 citations Open access
Semantic Scholar
DNA Damage Signaling Instructs Polyploid Macrophage Fate in Granulomas.
Laura Herrtwich, I. Nanda, K. Evangelou, T. Nikolova +34 more
2018Cell27 citations Open access
Semantic Scholar
Expanding the clinical phenotype of IARS2-related mitochondrial disease
B. Vona, R. Maroofian, E. Bellacchio, M. Najafi +19 more
2018BMC Medical Genetics26 citations Open access
Semantic Scholar
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans
B. Vona, Neda Mazaheri, Sheng-Jia Lin, Lucy A Dunbar +22 more
2021Human Genetics25 citations Open access
Semantic Scholar
Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors
R. Potabattula, M. Dittrich, Julia Böck, Larissa Haertle +5 more
2018Epigenomics25 citations Open access
Semantic Scholar
Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia.
A. Kariminejad, E. Szenker-Ravi, Caroline Lekszas, H. Tajsharghi +16 more
2019American Journal of Human Genetics24 citations Open access
Semantic Scholar
Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation
A. Ziegler, R. Duclaux-Loras, Céline Revenu, F. Charbit-Henrion +43 more
2021American Journal of Human Genetics23 citations Open access
Semantic Scholar
Non-syndromic hearing loss: clinical and diagnostic challenges
B. Vona, Julia Doll, Michaela A. H. Hofrichter, T. Haaf
2020Medizinische Genetik23 citations Open access
Semantic Scholar
Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line Authentication
I. Nanda, C. Steinlein, T. Haaf, E. M. Buhl +5 more
2022Cells20 citations Open access
Semantic Scholar
Ribosomal DNA methylation in human and mouse oocytes increases with age
R. Potabattula, T. Trapphoff, M. Dittrich, K. Fic +3 more
2022Aging19 citations Open access
Semantic Scholar
Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment
Paulina Bahena, N. Daftarian, R. Maroofian, Paola Linares +22 more
2021Human Genetics19 citations Open access
Semantic Scholar
Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation‐negative early‐onset and high‐risk breast cancer patients
Julia Böck, S. Appenzeller, Larissa Haertle, T. Schneider +7 more
2018International Journal of Cancer19 citations Open access
Semantic Scholar
The First Inherited Retinal Disease Registry in Iran: Research Protocol and Results of a Pilot Study.
Hamideh Sabbaghi, N. Daftarian, Fatemeh Suri, M. Mirrahimi +26 more
2020Archives of Iranian medicine17 citations Open access
Semantic Scholar
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer’s disease-related dysregulation
Larissa Haertle, Tobias Müller, R. Lardenoije, Anna Maierhofer +18 more
2019Clinical Epigenetics17 citations Open access
Semantic Scholar
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function
Sheng-Jia Lin, B. Vona, Hillary M Porter, M. Izadi +21 more
2022Human Mutation16 citations Open access
Semantic Scholar
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
Julia Doll, B. Vona, Linda Schnapp, F. Rüschendorf +20 more
2020Genes16 citations Open access
Semantic Scholar
Single Nucleotide Variants and Epimutations Induce Proteasome Inhibitor Resistance in Multiple Myeloma.
L. Haertle, S. Barrio, U. Munawar, Seung-Bin Han +25 more
2022Clinical Cancer Research15 citations Open access
Semantic Scholar
A piggyBac-based platform for genome editing and clonal rhesus macaque iPSC line derivation
Ignacio Rodríguez-Polo, S. Mißbach, S. Petkov, F. Mattern +8 more
2021Scientific Reports15 citations Open access
Semantic Scholar
Genome-wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between cytosine-phosphate-guanine methylation and histological subtypes
D. Fiedler, D. Hirsch, N. El Hajj, H. Yang +9 more
2019Genes, Chromosomes and Cancer15 citations Open access
Semantic Scholar
Prenatal and postnatal experiences associated with epigenetic changes in the adult mouse brain
F. Mattern, A. Post, F. Solger, A. O'Leary +3 more
2019Behavioural Brain Research15 citations Open access
Semantic Scholar
Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family
B. Vona, Reza Maroofian, G. Mendiratta, M. Croken +8 more
2017Molecular Syndromology14 citations Open access
Semantic Scholar
Phenotypic Characterization of DFNB16-associated Hearing Loss.
D. Back, W. Shehata-Dieler, B. Vona, Michaela A. H. Hofrichter +5 more
2019Otology and Neurotology13 citations
Semantic Scholar
Species-Specific Paternal Age Effects and Sperm Methylation Levels of Developmentally Important Genes
A. Prell, Mustafa Orkun Sen, R. Potabattula, Laura Bernhardt +7 more
2022Cells12 citations Open access
Semantic Scholar
Evolution of the Degenerated Y-Chromosome of the Swamp Guppy, Micropoecilia picta
I. Nanda, Susanne Schories, I. Simeonov, M. Adolfi +5 more
2022Cells12 citations Open access
Semantic Scholar
A genome-wide transcriptomic analysis of embryos fathered by obese males in a murine model of diet-induced obesity
Laura Bernhardt, M. Dittrich, Rabih El-Merahbi, A. Saliba +7 more
2021Scientific Reports12 citations Open access
Semantic Scholar

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