Charlotte von der Lippe

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 4

Top Topics

Systematic Review

Gene Expression

Atrial Fibrillation

Top Venues

Molecular genetics & genomic medicine

Qualitative health research

American journal of medical genetics. Part A

Orphanet journal of rare diseases

Telemark Hospital

University of Oslo (PHD)

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

Affiliation History

Telemark Hospital Mar 01 2019

Norway

Senior consultant :: Medical Genetics

Oslo University Hospital Aug 01 2010

Norway

Senior consultant/researcher :: Centre for Rare Disorders

Education History

University of Oslo Jan 10 2012 - Dec 07 2018

Norway

PHD

Publications

Charlotte von der Lippe, Ingrid Neteland, Kristin Billaud Feragen
Children with a rare congenital genetic disorder: a systematic review of parent experiences. Orphanet journal of rare diseases 17 (1) (2022)
Charlotte von der Lippe, Kristian Tveten, Trine E Prescott, Øystein L Holla, Øyvind L Busk, Katherine B Burke, Francis H Sansbury, Júlia Baptista, Andrew E Fry, Derek Lim, Stephen R A Jolles, Jennifer Evans, Deborah Osio, Carol Macmillan, Irene Bruno, Flavio Faltera, Salvador Climent, Roser Urreizti, Janet Hoenicka, Francesc Palau, Ana S A Cohen, Kendra Engleman, Dihong Zhou, Shivarajan M Amudhavalli, Médéric Jeanne, Frédérique Bonnet-Brilhault, Jonathan Lévy, Séverine Drunat, Nicolas Derive, Marte G Haug, Wenche Moe Thorstensen
Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin. American journal of medical genetics. Part A (2021)
Katrine K Brede, Margareta Wandel, Ingrid Wiig, Charlotte von der Lippe
Primary Immunodeficiency Diseases and Gastrointestinal Distress: Coping Strategies and Dietary Experiences to Relieve Symptoms. Qualitative health research 31 (2) (2020)
Charlotte von der Lippe, Plata S Diesen, Kristin B Feragen
Living with a rare disorder: a systematic review of the qualitative literature. Molecular genetics & genomic medicine 5 (6) (2017)