Anne Gregor

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Venues

Scientific reports

Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

American journal of medical genetics. Part A

Human molecular genetics

Rockefeller University

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

Affiliation History

Rockefeller University Jan 01 2014 - Dec 31 2017

United States

PostDoc :: Laboratory of Pediatric Brain Disease

University Hospital Erlangen Jan 01 2010 - Dec 31 2014

Germany

PhD student :: Institute of Human Genetics

Publications

Matthias Christen, Anne Gregor, Rodrigo Gutierrez Quintana, Jos Jacqueline Bongers, Angie Rupp, Jacques Penderis, G Diane Shelton, Vidhya Jagannathan, Christiane Zweier, Tosso Leeb
NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. Scientific reports 14 (1) (2024)
Matthias Christen, Anne Gregor, Rodrigo Gutierrez Quintana, Jos Jacqueline Bongers, Angie Rupp, Jacques Penderis, G Diane Shelton, Vidhya Jagannathan, Christiane Zweier, Tosso Leeb
NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. Scientific reports 14 (1) (2024)
Matthias Christen, Anne Gregor, Rodrigo Gutierrez Quintana, Jos Jacqueline Bongers, Angie Rupp, Jacques Penderis, G Diane Shelton, Vidhya Jagannathan, Christiane Zweier, Tosso Leeb
NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. Scientific reports 14 (1) (2024)
Matthias Christen, Anne Gregor, Rodrigo Gutierrez Quintana, Jos Jacqueline Bongers, Angie Rupp, Jacques Penderis, G Diane Shelton, Vidhya Jagannathan, Christiane Zweier, Tosso Leeb
NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. Scientific reports 14 (1) (2024)
Matthias Christen, Anne Gregor, Rodrigo Gutierrez Quintana, Jos Jacqueline Bongers, Angie Rupp, Jacques Penderis, G Diane Shelton, Vidhya Jagannathan, Christiane Zweier, Tosso Leeb
NDUFS7 variant in dogs with Leigh syndrome and its functional validation in a Drosophila melanogaster model. Scientific reports 14 (1) (2024)
Anne Gregor, Christiane Zweier
Modelling phenotypes, variants and pathomechanisms of syndromic diseases in different systems. Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V 36 (2) (2024)
Anne Gregor, Christiane Zweier
Modelling phenotypes, variants and pathomechanisms of syndromic diseases in different systems. Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V 36 (2) (2024)
M Makenzie Beaman, Lucia Guidugli, Monia Hammer, Chelsea Barrows, Anne Gregor, Sangmoon Lee, Kristen L Deak, Marie T McDonald, Courtney Jensen, Maha Saad Zaki, Amira T Masri, Charlotte A Hobbs, Joseph G Gleeson, Jennifer L Cohen
Novel association of Dandy-Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome. American journal of medical genetics. Part A (2023)
Anne Gregor, Tanja Meerbrei, Thorsten Gerstner, Annick Toutain, Sally Ann Lynch, Karen Stals, Caroline Maxton, Johannes R Lemke, John A Bernat, Hannah M Bombei, Nicola Foulds, David Hunt, Alma Kuechler, Jasmin Beygo, Petra Stöbe, Arjan Bouman, Maria Palomares-Bralo, Fernando Santos-Simarro, Sixto Garcia-Minaur, Marta Pacio-Miguez, Bernt Popp, Georgia Vasileiou, Moritz Hebebrand, André Reis, Sarah Schuhmann, Mandy Krumbiegel, Natasha J Brown, Peter Sparber, Lyusya Melikyan, Liudmila Bessonova, Tatiana Cherevatova, Artem Sharkov, Natalia Shcherbakova, Tabib Dabir, Usha Kini, Eva M C Schwaibold, Tobias B Haack, Marta Bertoli, Sabine Hoffjan, Ruth Falb, Marwan Shinawi, Heinrich Sticht, Christiane Zweier
De novo missense variants in FBXO11 alter its protein expression and subcellular localization. Human molecular genetics (2021)
Enrico D H Konrad, Niels Nardini, Almuth Caliebe, Inga Nagel, Dana Young, Gabriella Horvath, Stephanie L Santoro, Christine Shuss, Alban Ziegler, Dominique Bonneau, Marlies Kempers, Rolph Pfundt, Eric Legius, Arjan Bouman, Kyra E Stuurman, Katrin Õunap, Sander Pajusalu, Monica Hsiung Wojcik, Georgia Vasileiou, Gwenaël Le Guyader, Hege M Schnelle, Siren Berland, Evelien Zonneveld-Huijssoon, Simone Kersten, Aditi Gupta, Patrick R Blackburn, Marissa S Ellingson, Matthew J Ferber, Radhika Dhamija, Eric W Klee, Meriel McEntagart, Klaske D Lichtenbelt, Amy Kenney, Samantha A Vergano, Rami Abou Jamra, Konrad Platzer, Mary Ella Pierpont, Divya Khattar, Robert J Hopkin, Richard J Martin, Marjolijn C J Jongmans, Vivian Y Chang, Julian A Martinez-Agosto, Outi Kuismin, Mitja I Kurki, Olli Pietiläinen, Aarno Palotie, Timothy J Maarup, Diana S Johnson, Katja Venborg Pedersen, Lone W Laulund, Sally A Lynch, Moira Blyth, Katrina Prescott, Natalie Canham, Rita Ibitoye, Eva H Brilstra, Marwan Shinawi, Emily Fassi, null null, Heinrich Sticht, Anne Gregor, Hilde Van Esch, Christiane Zweier
CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (2019)

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Publication Activity (10 Years)

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Anne Gregor