Andreas David Zimmer (A Zimmer, Andreas D Zimmer, A D Zimmer, Andreas Zimmer)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Venues

The British journal of dermatology

European journal of human genetics : EJHG

Genes

Human mutation

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

Publications

Alexandra Baumann, Christian Ruckert, Christoph Meier, Tim Hutschenreiter, Robert Remy, Benedikt Schnur, Marvin Döbel, Rudel Christian Nkouamedjo Fankep, Dariush Skowronek, Oliver Kutz, Norbert Arnold, Anna-Lena Katzke, Michael Forster, Anna-Lena Kobiela, Katharina Thiedig, Andreas David Zimmer, Julia Ritter, Bernhard Heinrich Friedrich Weber, Ellen Honisch, Karl Hackmann, null null, Gunnar Schmidt, Marc Sturm, Corinna Ernst
Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score loci. European journal of human genetics : EJHG 32 (8) (2024)
Alexandra Baumann, Christian Ruckert, Christoph Meier, Tim Hutschenreiter, Robert Remy, Benedikt Schnur, Marvin Döbel, Rudel Christian Nkouamedjo Fankep, Dariush Skowronek, Oliver Kutz, Norbert Arnold, Anna-Lena Katzke, Michael Forster, Anna-Lena Kobiela, Katharina Thiedig, Andreas David Zimmer, Julia Ritter, Bernhard Heinrich Friedrich Weber, Ellen Honisch, Karl Hackmann, null null, Gunnar Schmidt, Marc Sturm, Corinna Ernst
Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score loci. European journal of human genetics : EJHG (2024)
Alexandra Baumann, Christian Ruckert, Christoph Meier, Tim Hutschenreiter, Robert Remy, Benedikt Schnur, Marvin Döbel, Rudel Christian Nkouamedjo Fankep, Dariush Skowronek, Oliver Kutz, Norbert Arnold, Anna-Lena Katzke, Michael Forster, Anna-Lena Kobiela, Katharina Thiedig, Andreas David Zimmer, Julia Ritter, Bernhard Heinrich Friedrich Weber, Ellen Honisch, Karl Hackmann, null null, Gunnar Schmidt, Marc Sturm, Corinna Ernst
Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score loci. European journal of human genetics : EJHG 32 (8) (2024)
Alexandra Baumann, Christian Ruckert, Christoph Meier, Tim Hutschenreiter, Robert Remy, Benedikt Schnur, Marvin Döbel, Rudel Christian Nkouamedjo Fankep, Dariush Skowronek, Oliver Kutz, Norbert Arnold, Anna-Lena Katzke, Michael Forster, Anna-Lena Kobiela, Katharina Thiedig, Andreas David Zimmer, Julia Ritter, Bernhard Heinrich Friedrich Weber, Ellen Honisch, Karl Hackmann, null null, Gunnar Schmidt, Marc Sturm, Corinna Ernst
Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score loci. European journal of human genetics : EJHG 32 (8) (2024)
Alexandra Baumann, Christian Ruckert, Christoph Meier, Tim Hutschenreiter, Robert Remy, Benedikt Schnur, Marvin Döbel, Rudel Christian Nkouamedjo Fankep, Dariush Skowronek, Oliver Kutz, Norbert Arnold, Anna-Lena Katzke, Michael Forster, Anna-Lena Kobiela, Katharina Thiedig, Andreas David Zimmer, Julia Ritter, Bernhard Heinrich Friedrich Weber, Ellen Honisch, Karl Hackmann, null null, Gunnar Schmidt, Marc Sturm, Corinna Ernst
Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score loci. European journal of human genetics : EJHG 32 (8) (2024)
Alrun Hotz, Julia Kopp, Emmanuelle Bourrat, Vinzenz Oji, Kira Süßmuth, Katalin Komlosi, Bakar Bouadjar, Iliana Tantcheva-Poór, Maritta Hellström Pigg, Regina C Betz, Kathrin Giehl, Fiona Schedel, Lisa Weibel, Solveig Schulz, Dora V Stölzl, Gianluca Tadini, Emine Demiral, Karin Berggard, Andreas David Zimmer, Svenja Alter, Judith Fischer
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis. Genes 14 (3) (2023)
Mingfeng Li, Kenneth Lay, Andreas David Zimmer, Kristin Technau-Hafsi, Jasmine Wong, Antonia Reimer, Jan Rohr, Ebtesam Abdalla, Judith Fischer, Bruno Reversade, Cristina Has
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. The British journal of dermatology 188 (2) (2023)
Mingfeng Li, Kenneth Lay, Andreas David Zimmer, Kristin Technau-Hafsi, Jasmine Wong, Antonia Reimer, Jan Rohr, Ebtesam Abdalla, Judith Fischer, Bruno Reversade, Cristina Has
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. The British journal of dermatology 188 (2) (2023)
Alrun Hotz, Julia Kopp, Emmanuelle Bourrat, Vinzenz Oji, Kira Süßmuth, Katalin Komlosi, Bakar Bouadjar, Iliana Tantcheva-Poór, Maritta Hellström Pigg, Regina C Betz, Kathrin Giehl, Fiona Schedel, Lisa Weibel, Solveig Schulz, Dora V Stölzl, Gianluca Tadini, Emine Demiral, Karin Berggard, Andreas David Zimmer, Svenja Alter, Judith Fischer
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis. Genes 14 (3) (2023)
Sabine Jägle, Hao-Hsiang Hsu, Hazem A Juratli, Andreas David Zimmer, Amelie Prieschl, Svenja Alter, Bernhard Wiedenhofer, Dieter Metze, Steffen Emmert, Judith Fischer
Pathogenic variants in the SPTLC1 gene cause hyperkeratosis lenticularis perstans. The British journal of dermatology 188 (1) (2023)
Mingfeng Li, Kenneth Lay, Andreas David Zimmer, Kristin Technau-Hafsi, Jasmine Wong, Antonia Reimer, Jan Rohr, Ebtesam Abdalla, Judith Fischer, Bruno Reversade, Cristina Has
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. The British journal of dermatology 188 (2) (2023)
Alrun Hotz, Julia Kopp, Emmanuelle Bourrat, Vinzenz Oji, Kira Süßmuth, Katalin Komlosi, Bakar Bouadjar, Iliana Tantcheva-Poór, Maritta Hellström Pigg, Regina C Betz, Kathrin Giehl, Fiona Schedel, Lisa Weibel, Solveig Schulz, Dora V Stölzl, Gianluca Tadini, Emine Demiral, Karin Berggard, Andreas David Zimmer, Svenja Alter, Judith Fischer
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis. Genes 14 (3) (2023)
Leonie Frommherz, Katalin Komlosi, Charlotte Hewel, Julia Kopp, Malin Dewenter, Andreas David Zimmer, Oliver Bartsch, Matthias Linke, Kristin Technau-Hafsi, Susanne Gerber, Judith Fischer, Cristina Has
Acral lamellar ichthyosis with amino acid substitution in the C-terminus of keratin 2. Journal of the European Academy of Dermatology and Venereology : JEADV (2022)
Luise D Resch, Alrun Hotz, Andreas David Zimmer, Katalin Komlosi, Nina Singh, Andreas Tzschach, Marisa Windfuhr-Blum, Ingolf Juhasz-Boess, Thalia Erbes, Judith Fischer, Svenja Alter
The Importance of Extended Analysis Using Current Molecular Genetic Methods Based on the Example of a Cohort of 228 Patients with Hereditary Breast and Ovarian Cancer Syndrome. Genes 12 (10) (2021)
Alrun Hotz, Julia Kopp, Emmanuelle Bourrat, Vinzenz Oji, Katalin Komlosi, Kathrin Giehl, Bakar Bouadjar, Anette Bygum, Iliana Tantcheva-Poor, Maritta Hellström Pigg, Cristina Has, Zhou Yang, Alan D Irvine, Regina C Betz, Giovanna Zambruno, Gianluca Tadini, Kira Süßmuth, Robert Gruber, Matthias Schmuth, Juliette Mazereeuw-Hautier, Natalie Jonca, Sophie Guez, Michela Brena, Angela Hernandez-Martin, Peter van den Akker, Maria C Bolling, Katariina Hannula-Jouppi, Andreas David Zimmer, Svenja Alter, Anders Vahlquist, Judith Fischer
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients. Genes 12 (1) (2021)
Julia Vornweg, S Gläser, M Ahmad-Anwar, Andreas David Zimmer, M Kuhn, S Hörer, G C Korenke, J Grothaus, H Ott, Judith Fischer
Identification of compound heterozygous mutations in AP1B1 leading to the newly described recessive keratitis-ichthyosis-deafness (KIDAR) syndrome. The British journal of dermatology 184 (6) (2021)
Svenja Alter, Andreas David Zimmer, Misun Park, Jianli Gong, Almuth Caliebe, Regina Fölster-Holst, Antonio Torrelo, Isabel Colmenero, Susan F Steinberg, Judith Fischer
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in protein kinase D1. Journal of medical genetics 58 (6) (2020)
L Frommherz, J Küsel, Andreas David Zimmer, J Fischer, Cristina Has
Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosis. The British journal of dermatology 182 (3) (2019)
Nadja Ballin, Alrun Hotz, Emmanuelle Bourrat, Julia Küsel, Vinzenz Oji, Bakar Bouadjar, Davide Brognoli, Geoffroy Hickman, Lisa Heinz, Pierre Vabres, Slaheddine Marrakchi, Stéphanie Leclerc-Mercier, Alan Irvine, Gianluca Tadini, Henning Hamm, Cristina Has, Ulrike Blume-Peytavi, Diana Mitter, Marina Reitenbach, Ingrid Hausser, Andreas David Zimmer, Svenja Alter, Judith Fischer
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4. Human mutation 40 (12) (2019)
Lisa Heinz, E Bourrat, P Vabres, J Thevenon, Alrun Hotz, S Hörer, J Küsel, Andreas David Zimmer, S Alter, R Happle, Judith Fischer
Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia. The British journal of dermatology 180 (3) (2018)

Andreas David Zimmer.css-eqlu8i{font-size:small;padding-left:4px;} (A Zimmer, Andreas D Zimmer, A D Zimmer, Andreas Zimmer)

Publication Activity (10 Years)

Top Topics

Top Venues

Andreas David Zimmer (A Zimmer, Andreas D Zimmer, A D Zimmer, Andreas Zimmer)