Thomas Haaf

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 30

Top Topics

Multiple Myeloma

Dna Methylation

Top Venues

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Asuman Koparir, Caroline Lekszas, Kemal Keseroğlu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome. Human genomics 18 (1) (2024)
Marcus Dittrich, Laura Bernhardt, Christopher A Penfold, Thorsten E Boroviak, Charis Drummer, Rüdiger Behr, Tobias Müller, Thomas Haaf
Age-related and species-specific methylation changes in the protein-coding marmoset sperm epigenome. Aging cell 23 (8) (2024)
Asuman Koparir, Caroline Lekszas, Kemal Keseroğlu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome. Human genomics 18 (1) (2024)
Asuman Koparir, Caroline Lekszas, Kemal Keseroğlu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome. Human genomics 18 (1) (2024)
Ramya Potabattula, Jana Durackova, Sarah Kießling, Alina Michler, Thomas Hahn, Martin Schorsch, Tom Trapphoff, Stefan Dieterle, Thomas Haaf
D4Z4 Hypomethylation in Human Germ Cells. Cells 13 (17) (2024)
Marcus Dittrich, Laura Bernhardt, Christopher A Penfold, Thorsten E Boroviak, Charis Drummer, Rüdiger Behr, Tobias Müller, Thomas Haaf
Age-related and species-specific methylation changes in the protein-coding marmoset sperm epigenome. Aging cell 23 (8) (2024)
Marcus Dittrich, Laura Bernhardt, Christopher A Penfold, Thorsten E Boroviak, Charis Drummer, Rüdiger Behr, Tobias Müller, Thomas Haaf
Age-related and species-specific methylation changes in the protein-coding marmoset sperm epigenome. Aging cell 23 (8) (2024)
Marcus Dittrich, Laura Bernhardt, Christopher A Penfold, Thorsten E Boroviak, Charis Drummer, Rüdiger Behr, Tobias Müller, Thomas Haaf
Age-related and species-specific methylation changes in the protein-coding marmoset sperm epigenome. Aging cell (2024)
Kiara Gäberlein, Sarah K Schröder, Indrajit Nanda, Claus Steinlein, Thomas Haaf, Eva M Buhl, Sauvant Patrick, Vincent Sapin, Armando Abergel, Ralf Weiskirchen
Genetic Characterization of Rat Hepatic Stellate Cell Line PAV-1. Cells 12 (12) (2023)
Kiara Gäberlein, Sarah K Schröder, Indrajit Nanda, Claus Steinlein, Thomas Haaf, Eva M Buhl, Sauvant Patrick, Vincent Sapin, Armando Abergel, Ralf Weiskirchen
Genetic Characterization of Rat Hepatic Stellate Cell Line PAV-1. Cells 12 (12) (2023)
Kiara Gäberlein, Sarah K Schröder, Indrajit Nanda, Claus Steinlein, Thomas Haaf, Eva M Buhl, Sauvant Patrick, Vincent Sapin, Armando Abergel, Ralf Weiskirchen
Genetic Characterization of Rat Hepatic Stellate Cell Line PAV-1. Cells 12 (12) (2023)
Indrajit Nanda, Sarah K Schröder, Claus Steinlein, Thomas Haaf, Eva M Buhl, Dominik G Grimm, Ralf Weiskirchen
Rat Hepatic Stellate Cell Line CFSC-2G: Genetic Markers and Short Tandem Repeat Profile Useful for Cell Line Authentication. Cells 11 (18) (2022)
Andreas Prell, Mustafa Orkun Sen, Ramya Potabattula, Laura Bernhardt, Marcus Dittrich, Thomas Hahn, Martin Schorsch, Federica Zacchini, Grazyna Ewa Ptak, Heiner Niemann, Thomas Haaf
Species-Specific Paternal Age Effects and Sperm Methylation Levels of Developmentally Important Genes. Cells 11 (4) (2022)
Indrajit Nanda, Susanne Schories, Ivan Simeonov, Mateus Contar Adolfi, Kang Du, Claus Steinlein, Manfred Alsheimer, Thomas Haaf, Manfred Schartl
Evolution of the Degenerated Y-Chromosome of the Swamp Guppy, Micropoecilia picta . Cells 11 (7) (2022)
Renzo J M Riemens, Gunter Kenis, Jennifer Nolz, Sonia C Susano Chaves, Diane Duroux, Ehsan Pishva, Diego Mastroeni, Kristel Van Steen, Thomas Haaf, Daniel L A van den Hove
Targeted Methylation Profiling of Single Laser-Capture Microdissected Post-Mortem Brain Cells by Adapted Limiting Dilution Bisulfite Pyrosequencing (LDBSP). International journal of molecular sciences 23 (24) (2022)
Larissa Haertle, Santiago Barrio, Umair Munawar, Seungbin Han, Xiang Zhou, Michal Simicek, Cornelia Vogt, Marietta Truger, Rafael Alonso Fernández, Maximilian Johannes Steinhardt, Julia Weingart, Renata Snaurova, Silvia Nerreter, Eva Teufel, Andoni Garitano-Trojaola, Matteo Claudio Da Via, Yanira Ruiz-Heredia, Andreas Rosenwald, Niccolo' Bolli, Roman Hájek, Peter Raab, Marc-Steffen Raab, Niels Weinhold, Claudia Haferlach, Thomas Haaf, Joaquin Martinez Lopez, Hermann Einsele, Leo Rasche, Klaus Martin Kortüm
Single Nucleotide Variants and Epimutations Induce Proteasome Inhibitor Resistance in Multiple Myeloma. Clinical cancer research : an official journal of the American Association for Cancer Research (2022)
Indrajit Nanda, Claus Steinlein, Thomas Haaf, Eva M Buhl, Dominik G Grimm, Scott L Friedman, Steffen K Meurer, Sarah K Schröder, Ralf Weiskirchen
Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line Authentication. Cells 11 (11) (2022)
Renzo J M Riemens, Gunter Kenis, Jennifer Nolz, Sonia C Susano Chaves, Diane Duroux, Ehsan Pishva, Diego Mastroeni, Kristel Van Steen, Thomas Haaf, Daniel L A van den Hove
Targeted Methylation Profiling of Single Laser-Capture Microdissected Post-Mortem Brain Cells by Adapted Limiting Dilution Bisulfite Pyrosequencing (LDBSP). International journal of molecular sciences 23 (24) (2022)
Yosra Bejaoui, Aleem Razzaq, Noha A Yousri, Junko Oshima, Andre Megarbane, Abeer Qannan, Ramya Potabattula, Tanvir Alam, George M Martin, Henning F Horn, Thomas Haaf, Steve Horvath, Nady El Hajj
DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome. Aging cell 21 (2) (2022)
Renzo J M Riemens, Gunter Kenis, Jennifer Nolz, Sonia C Susano Chaves, Diane Duroux, Ehsan Pishva, Diego Mastroeni, Kristel Van Steen, Thomas Haaf, Daniel L A van den Hove
Targeted Methylation Profiling of Single Laser-Capture Microdissected Post-Mortem Brain Cells by Adapted Limiting Dilution Bisulfite Pyrosequencing (LDBSP). International journal of molecular sciences 23 (24) (2022)
Paulina Bahena, Narsis Daftarian, Reza Maroofian, Paola Linares, Daniel Villalobos, Mehraban Mirrahimi, Aboulfazl Rad, Julia Doll, Michaela A H Hofrichter, Asuman Koparir, Tabea Röder, Seungbin Han, Hamideh Sabbaghi, Hamid Ahmadieh, Hassan Behboudi, Cristina Villanueva-Mendoza, Vianney Cortés-Gonzalez, Rocio Zamora-Ortiz, Susanne Kohl, Laura Kuehlewein, Hossein Darvish, Elham Alehabib, Maria de la Luz Arenas-Sordo, Fatemeh Suri, Barbara Vona, Thomas Haaf
Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment. Human genetics (2021)
Larissa Haertle, Santiago Barrio, Umair Munawar, Seungbin Han, Xiang Zhou, Cornelia Vogt, Rafael Alonso Fernández, Markus Krebs, Yanira Ruiz-Heredia, Matteo Claudio Da Via, Josip Zovko, Andoni Garitano-Trojaola, Niccolò Bolli, Anna Ruckdeschel, Thorsten Stühmer, Manik Chatterjee, Miriam Kull, Jan Krönke, Xabier Agirre, Jose I Martin-Subero, Peter Raab, Hermann Einsele, Leo Rasche, Joaquin Martinez-Lopez, Thomas Haaf, Klaus Martin Kortüm
Cereblon enhancer methylation and IMiD resistance in multiple myeloma. Blood 138 (18) (2021)
Barbara Vona, Neda Mazaheri, Sheng-Jia Lin, Lucy A Dunbar, Reza Maroofian, Hela Azaiez, Kevin T A Booth, Sandrine Vitry, Aboulfazl Rad, Franz Rüschendorf, Pratishtha Varshney, Ben Fowler, Christian Beetz, Kumar N Alagramam, David P Murphy, Gholamreza Shariati, Alireza Sedaghat, Henry Houlden, Cassidy Petree, Shruthi VijayKumar, Richard J H Smith, Thomas Haaf, Aziz El-Amraoui, Michael R Bowl, Guarav K Varshney, Hamid Galehdari
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans. Human genetics 140 (6) (2021)
Julia Doll, Barbara Vona, Linda Schnapp, Franz Rüschendorf, Imran Khan, Saadullah Khan, Noor Muhammad, Sher Alam Khan, Hamed Nawaz, Ajmal Khan, Naseer Ahmad, Susanne M Kolb, Laura Kuehlewein, Jonathan D J Labonne, Lawrence C Layman, Michaela A H Hofrichter, Tabea Röder, Marcus Dittrich, Tobias Müller, Tyler D Graves, Il-Keun Kong, Indrajit Nanda, Hyung-Goo Kim, Thomas Haaf
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families. Genes 11 (11) (2020)
Julia Doll, Michaela A H Hofrichter, Paulina Bahena, Alfred Heihoff, Dennis Segebarth, Tobias Müller, Marcus Dittrich, Thomas Haaf, Barbara Vona
A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family. Molecular genetics & genomic medicine 8 (8) (2020)
Ramya Potabattula, Federica Zacchini, Grazyna Ewa Ptak, Marcus Dittrich, Tobias Müller, Nady El Hajj, Thomas Hahn, Charis Drummer, Rüdiger Behr, Andrea Lucas-Hahn, Heiner Niemann, Martin Schorsch, Thomas Haaf
Increasing methylation of sperm rDNA and other repetitive elements in the aging male mammalian germline. Aging cell 19 (8) (2020)
Caroline Lekszas, Ombretta Foresti, Ishier Raote, Daniel Liedtke, Eva-Maria König, Indrajit Nanda, Barbara Vona, Peter De Coster, R G E C Cauwels, Vivek Malhotra, Thomas Haaf
Biallelic TANGO1 mutations cause a novel syndromal disease due to hampered cellular collagen secretion. eLife 9 (2020)
Caroline Lekszas, Indrajit Nanda, Barbara Vona, Julia Böck, Farah Ashrafzadeh, Nahid Donyadideh, Farnoosh Ebrahimzadeh, Najmeh Ahangari, Reza Maroofian, Ehsan Ghayoor Karimiani, Thomas Haaf
Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report. BMC medical genomics 12 (1) (2019)
Anna Maierhofer, Julia Flunkert, Junko Oshima, George M Martin, Martin Poot, Indrajit Nanda, Marcus Dittrich, Tobias Müller, Thomas Haaf
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes. Aging cell 18 (5) (2019)
Julia Böck, Silke Appenzeller, Larissa Haertle, Tamara Schneider, Andrea Gehrig, Jörg Schröder, Simone Rost, Beat Wolf, Claus R Bartram, Christian Sutter, Thomas Haaf
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. International journal of cancer 143 (6) (2018)