Ines Kapferer‐Seebacher

The 2017 international classification of the Ehlers–Danlos syndromes

Fransiska Malfait, Clair A. Francomano, Peter H. Byers et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2017 · 1.9K citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , which Encode Subcomponents C1r and C1s of Complement

Ines Kapferer‐Seebacher, Melanie Pepin, Roland Werner et al. · The American Journal of Human Genetics · 2016 · 119 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

<i>SLC13A5</i> is the second gene associated with Kohlschütter–Tönz syndrome

Anna Schossig, Agnès Bloch‐Zupan, Adrian Lussi et al. · Journal of Medical Genetics · 2016 · 56 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome

Rebekka Gröbner, Ines Kapferer‐Seebacher, Albert Amberger et al. · Frontiers in Immunology · 2019 · 31 citations · Full text

Life Sciences, Immunology, Molecular Biology +17

Prospective clinical investigations of children with periodontal Ehlers–Danlos syndrome identify generalized lack of attached gingiva as a pathognomonic feature

Ines Kapferer‐Seebacher, Elizabeth Oakley-Hannibal, Ulrike Lepperdinger et al. · Genetics in Medicine · 2020 · 31 citations · Full text

Dentistry, Periodontics, Periodontology +17