Andreas Laner (A Laner)

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 16

Top Venues

European journal of human genetics : EJHG

Movement disorders : official journal of the Movement Disorder Society

Genes

Familial cancer

Medizinisch Genetisches Zentrum

Technical University Munich (PHD)

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

Affiliation History

Medizinisch Genetisches Zentrum Feb 01 2002

Germany

Head :: Genomics Programm

Education History

Technical University Munich

Germany

PHD :: Human Gentics

Publications

Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG (2024)
Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (6) (2024)
Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (6) (2024)
Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (6) (2024)
Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG 32 (7) (2024)
Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG 32 (7) (2024)
Gunnar Houge, Eirik Bratland, Ingvild Aukrust, Kristian Tveten, Gabrielė Žukauskaitė, Ivona Sansovic, Alejandro J Brea-Fernández, Karin Mayer, Teija Paakkola, Caoimhe McKenna, William Wright, Milica Keckarevic Markovic, Dorte Launholt Lildballe, Michal Konecny, Thomas Smol, Pia Alhopuro, Estelle Arnaud Gouttenoire, Katharina Obeid, Albena Todorova, Milena Jankovic, Joanna M Lubieniecka, Maja Stojiljkovic, Marie-Pierre Buisine, Bjørn Ivar Haukanes, Marie Lorans, Hanno Roomere, François Mickaël Petit, Maria K Haanpää, Claire Beneteau, Belén Pérez, Dijana Plaseska-Karanfilska, Matthias Rath, Nico Fuhrmann, Bibiana I Ferreira, Coralea Stephanou, Wenche Sjursen, Aleš Maver, Cécile Rouzier, Adela Chiriță-Emandi, João Gonçalves, Wei Cheng David Kuek, Martin Broly, Lonneke Haer-Wigman, Meow-Keong Thong, Sok-Kun Tae, Michaela Hyblova, Johan T den Dunnen, Andreas Laner
Comparison of the ABC and ACMG systems for variant classification. European journal of human genetics : EJHG 32 (7) (2024)
Rauan Kaiyrzhanov, Juan Dario Ortigoza-Escobar, Brett W Stringer, Manizha Ganieva, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Alfons Macaya, Andreas Laner, Enas Onbool, Randa Al-Shammari, Mohammed Al-Owain, Nicolas Deconinck, Catheline Vilain, Pauline Dontaine, Eleanor Self, Rabia Akram, Ghulam Hussain, Shahid Mahmood Baig, Javed Iqbal, Vincenzo Salpietro, Maedeh Neshatdoust, Mahboubeh Kasiri, Gozde Yesil Sayın, Turkan Uygur, Karen Pysden, Ian R Berry, Cesar Augusto Alves, Jean Giacomotto, Henry Houlden, Reza Maroofian
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society (2024)
Alexander German, Jelena Jukic, Andreas Laner, Philipp Arnold, Eileen Socher, Angelika Barbara Mennecke, Manuel Alexander Schmidt, Juergen Winkler, Angela Abicht, Martin Regensburger
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes 15 (1) (2023)
Alexander German, Jelena Jukic, Andreas Laner, Philipp Arnold, Eileen Socher, Angelika Barbara Mennecke, Manuel Alexander Schmidt, Juergen Winkler, Angela Abicht, Martin Regensburger
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes 15 (1) (2023)
Alexander German, Jelena Jukic, Andreas Laner, Philipp Arnold, Eileen Socher, Angelika Barbara Mennecke, Manuel Alexander Schmidt, Juergen Winkler, Angela Abicht, Martin Regensburger
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes 15 (1) (2023)
Alexander German, Jelena Jukic, Andreas Laner, Philipp Arnold, Eileen Socher, Angelika Barbara Mennecke, Manuel Alexander Schmidt, Juergen Winkler, Angela Abicht, Martin Regensburger
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35). Genes 15 (1) (2023)
Monika Morak, Marta Pineda, Alexandra Martins, Pascaline Gaildrat, Hélène Tubeuf, Aurélie Drouet, Carolina Gómez, Estela Dámaso, Kerstin Schaefer, Verena Steinke-Lange, Udo Koehler, Andreas Laner, Julie Hauchard, Karine Chauris, Elke Holinski-Feder, Gabriel Capellá Munar
Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working Group. European journal of human genetics : EJHG 30 (9) (2022)
Teresa M Neuhann, Katharina Haub, Verena Steinke-Lange, Monika Morak, Andreas Laner, Melanie Locher, Elke Holinski-Feder
Long-term chemoprevention in patients with adenomatous polyposis coli: an observational study. Familial cancer 21 (4) (2022)
Monika Morak, Verena Steinke-Lange, Trisari Massdorf, Anna Benet-Pages, Melanie Locher, Andreas Laner, Katrin Kayser, Stefan Aretz, Elke Holinski-Feder
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics. Familial cancer 19 (2) (2021)
Andreas Laner, A Benet-Pages, B Neitzel, E Holinski-Feder
Analysis of 3297 individuals suggests that the pathogenic germline 5'-UTR variant BRCA1 c.-107A > T is not common in south-east Germany. Familial cancer 19 (3) (2020)

Andreas Laner.css-eqlu8i{font-size:small;padding-left:4px;} (A Laner)

Publication Activity (10 Years)

Top Topics

Top Venues

Andreas Laner (A Laner)