Ulrike Hüffmeier (U Hüffmeier)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 20

Top Topics

Atopic Dermatitis

Top Venues

European journal of human genetics : EJHG

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG

Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

BMC medical genetics

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

Publications

Fatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, Ulrike Hüffmeier, Melissa Pauly, André Reis, Laurence Faivre, Julien Maraval, Ange-Line Bruel, Frédéric Tran Mau Them, Tobias B Haack, Ute Grasshoff, Veronka Horber, Rachel Schot, Marjon van Slegtenhorst, Martina Wilke, Tahsin Stefan Barakat
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorder. European journal of human genetics : EJHG 32 (3) (2024)
Fatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, Ulrike Hüffmeier, Melissa Pauly, André Reis, Laurence Faivre, Julien Maraval, Ange-Line Bruel, Frédéric Tran Mau Them, Tobias B Haack, Ute Grasshoff, Veronka Horber, Rachel Schot, Marjon van Slegtenhorst, Martina Wilke, Tahsin Stefan Barakat
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorder. European journal of human genetics : EJHG 32 (3) (2024)
Fatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, Ulrike Hüffmeier, Melissa Pauly, André Reis, Laurence Faivre, Julien Maraval, Ange-Line Bruel, Frédéric Tran Mau Them, Tobias B Haack, Ute Grasshoff, Veronka Horber, Rachel Schot, Marjon van Slegtenhorst, Martina Wilke, Tahsin Stefan Barakat
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorder. European journal of human genetics : EJHG 32 (3) (2024)
Fatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, Ulrike Hüffmeier, Melissa Pauly, André Reis, Laurence Faivre, Julien Maraval, Ange-Line Bruel, Frédéric Tran Mau Them, Tobias B Haack, Ute Grasshoff, Veronka Horber, Rachel Schot, Marjon van Slegtenhorst, Martina Wilke, Tahsin Stefan Barakat
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorder. European journal of human genetics : EJHG 32 (3) (2024)
Fatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, Ulrike Hüffmeier, Melissa Pauly, André Reis, Laurence Faivre, Julien Maraval, Ange-Line Bruel, Frédéric Tran Mau Them, Tobias B Haack, Ute Grasshoff, Veronka Horber, Rachel Schot, Marjon van Slegtenhorst, Martina Wilke, Tahsin Stefan Barakat
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorder. European journal of human genetics : EJHG (2024)
Fatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, Ulrike Hüffmeier, Melissa Pauly, André Reis, Laurence Faivre, Julien Maraval, Ange-Line Bruel, Frédéric Tran Mau Them, Tobias B Haack, Ute Grasshoff, Veronka Horber, Rachel Schot, Marjon van Slegtenhorst, Martina Wilke, Tahsin Stefan Barakat
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorder. European journal of human genetics : EJHG (2024)
Vera Baur, Johanna Stoevesandt, Axel Hueber, Ulrike Hüffmeier, Hermann Kneitz, Henner Morbach, Erwin Schultz, Matthias Goebeler
VEXAS-Syndrom, eine neu beschriebene autoinflammatorische Systemerkrankung mit dermatologischen Manifestationen. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 21 (12) (2023)
Vera Baur, Johanna Stoevesandt, Axel Hueber, Ulrike Hüffmeier, Hermann Kneitz, Henner Morbach, Erwin Schultz, Matthias Goebeler
VEXAS-Syndrom, eine neu beschriebene autoinflammatorische Systemerkrankung mit dermatologischen Manifestationen. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 21 (12) (2023)
Vera Baur, Johanna Stoevesandt, Axel Hueber, Ulrike Hüffmeier, Hermann Kneitz, Henner Morbach, Erwin Schultz, Matthias Goebeler
VEXAS-Syndrom, eine neu beschriebene autoinflammatorische Systemerkrankung mit dermatologischen Manifestationen. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 21 (12) (2023)
Regina C Betz, Ulrike Hüffmeier
Dermatological diseases from a genetic perspective. Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V 35 (1) (2023)
Vera Baur, Johanna Stoevesandt, Axel Hueber, Ulrike Hüffmeier, Hermann Kneitz, Henner Morbach, Erwin Schultz, Matthias Goebeler
VEXAS-Syndrom, eine neu beschriebene autoinflammatorische Systemerkrankung mit dermatologischen Manifestationen. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 21 (12) (2023)
Ulrike Hüffmeier, Janine Klima, Mohammad Deen Hayatu
Genetic underpinnings of the psoriatic spectrum. Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V 35 (1) (2023)
Ulrike Hüffmeier, Janine Klima, Mohammad Deen Hayatu
Genetic underpinnings of the psoriatic spectrum. Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V 35 (1) (2023)
Stephanie Oates, Michael Absoud, Sushma Goyal, Sophie Bayley, Jennifer Baulcomb, Annemarie Sims, Amy Riddett, Katrina Allis, Charlotte Brasch-Andersen, Meena Balasubramanian, Renkui Bai, Bert Callewaert, Ulrike Hüffmeier, Diana Le Duc, Maximilian Radtke, Christian M Korff, Joanna Kennedy, Karen Jaqueline Low, Rikke Steensjerre Moller, Jens Erik Klint Nielsen, Bernt Popp, Lina Quteineh, Gitte Rønde, Bitten Schönewolf-Greulich, Amelle Shillington, Matthew R G Taylor, Emily Todd, Pernille Mathiesen Torring, Zeynep Tümer, Georgia Vasileiou, T Michael Yates, Christiane Zweier, Richard E Rosch, M Albert Basson, Deb K Pal
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. Clinical genetics 100 (4) (2021)
Ulrike Hüffmeier, Cornelia Kraus, Miriam S Reuter, Steffen Uebe, Mary-Alice Abbott, Syed A Ahmed, Kristyn L Rawson, Eileen Barr, Hong Li, Ange-Line Bruel, Laurence Faivre, Frédéric Tran Mau-Them, Christina Botti, Susan Brooks, Kaitlyn Burns, D Isum Ward, Marina Dutra-Clarke, Julian A Martinez-Agosto, Hane Lee, Stanley F Nelson, null null, Pia Zacher, Rami Abou Jamra, Chiara Klöckner, Julie McGaughran, Jürgen Kohlhase, Sarah Schuhmann, Ellen Moran, John Pappas, Annick Raas-Rothschild, Maria J Guillen Sacoto, Lindsay B Henderson, Timothy Blake Palculict, Sureni V Mullegama, Houda Zghal Elloumi, Adi Reich, Samantha A Schrier Vergano, Erica Wahl, André Reis, Christiane Zweier
EIF3F-related neurodevelopmental disorder: refining the phenotypic and expanding the molecular spectrum. Orphanet journal of rare diseases 16 (1) (2021)
Gunter Assmann, Michaela Köhm, Volker Schuster, Frank Behrens, Rotraut Mössner, Nina Magnolo, Vinzenz Oji, Harald Burkhardt, Ulrike Hüffmeier
Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups. BMC medical genetics 21 (1) (2020)
Rotraut Mössner, D Wilsmann-Theis, V Oji, P Gkogkolou, S Löhr, P Schulz, A Körber, J C Prinz, R Renner, K Schäkel, L Vogelsang, K-P Peters, S Philipp, Kristian Reich, H Ständer, A Jacobi, A Weyergraf, K Kingo, S Kõks, S Gerdes, K Steinz, T Schill, K G Griewank, M Müller, S Frey, L Ebertsch, S Uebe, M Sticherling, H Sticht, Ulrike Hüffmeier
The genetic basis for most patients with pustular skin disease remains elusive. The British journal of dermatology 178 (3) (2018)
Jianghong Zhong, Tatjana Scholz, Anthony C Y Yau, Simon Guerard, Ulrike Hüffmeier, Harald Burkhardt, Rickard Holmdahl
Mannan-induced Nos2 in macrophages enhances IL-17-driven psoriatic arthritis by innate lymphocytes. Science advances 4 (5) (2018)
R Sighart, Juergen Rech, Alexander Pfeil, Norbert Blank, S Löhr, André Reis, Heinrich Sticht, Ulrike Hüffmeier
Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes. Rheumatology international 38 (1) (2017)
Steffen Uebe, Maria Ehrlicher, Arif Bülent Ekici, Frank Behrens, Beate Böhm, Georg Homuth, Claudia Schurmann, Uwe Völker, Michael Jünger, Matthias Nauck, Henry Völzke, Heiko Traupe, Michael Krawczak, Harald Burkhardt, André Reis, Ulrike Hüffmeier
Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients. BMC medical genetics 18 (1) (2017)