Sheila Unger
Université de Lausanne
H-index: 53
Europe-Switzerland
Top articles of Sheila Unger
Exome sequencing and the identification of new genes and shared mechanisms in polymicrogyria
JAMA neurology
2023/9/1
Alisa Mo
H-Index: 4
Richard S Smith
H-Index: 19
Harrison Brand
H-Index: 21
Edward Yang
H-Index: 19
Annapurna Poduri
H-Index: 44
Christopher A Walsh
H-Index: 80
Stephen Brown
H-Index: 19
Michael Clarke
H-Index: 1
Andrew Green
H-Index: 21
Laila Mahmoud
H-Index: 8
Amira Masri
H-Index: 20
Dang Khoa Nguyen
H-Index: 5
Mustafa Sahin
H-Index: 2
Siddharth Srivastava
H-Index: 2
Sheila Unger
H-Index: 31
Thomas Voit
H-Index: 52
Cardiac hereditary diseases: genetic insights from a single center 15-year experience
Europace
2023/6
Cardiogenetics and Artificial Intelligence: the Mutscore Algorithm
Europace
2023/6
Nosology of genetic skeletal disorders: 2023 revision
American Journal of Medical Genetics Part A
2023/5
Sheila Unger
H-Index: 31
Christine Hall
H-Index: 4
Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage
The American Journal of Human Genetics
2023/4/6
Genetische Beratung: Konzepte, Missverständnisse, Perspektiven
Schweizerische Ärztezeitung (SÄZ)
2022/12/7
Thierry Nouspikel
H-Index: 13
Sheila Unger
H-Index: 31
Conseil génétique: concepts, malentendus et perspectives
Bulletin des médecins suisses
2022/12/7
Thierry Nouspikel
H-Index: 13
Sheila Unger
H-Index: 31
Molecular genetic diagnosis in children with cochlear implants in the Western french speaking part of Switzerland
Revue Medicale Suisse
2022/10/1
Sheila Unger
H-Index: 31
Christian Simon
H-Index: 5
Short telomere syndrome in adults: a rare entity that should be evoked
Revue Medicale Suisse
2022/8/1
Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicity
The American Journal of Human Genetics
2022/3/3
Katarina Cisarova
H-Index: 5
Beryl Royer-Bertrand
H-Index: 11
Sheila Unger
H-Index: 31
Andrea Superti-Furga
H-Index: 45
Clinical and molecular diagnosis of osteocraniostenosis in fetuses and newborns: Prenatal ultrasound, clinical, radiological and pathological features
2022/1/28
Making the right choice. How unaffected women carrying BRCA1/BRCA2 germline mutations decide for prophylactic mastectomy to reduce cancer risk
2022
Sheila Unger
H-Index: 31
Maria Caiata Zufferey
H-Index: 11
Chondrodysplasia and growth failure in children after early hematopoietic stem cell transplantation for non‐oncologic disorders
American Journal of Medical Genetics Part A
2021/2
Melita Irving
H-Index: 20
Ann Nordgren
H-Index: 30
Giedre Grigelioniene
H-Index: 20
Sheila Unger
H-Index: 31
Update Swiss guideline for counselling and testing for predisposition to breast, ovarian, pancreatic and prostate cancer
Swiss Medical Weekly
2021/9/13
Sheila Unger
H-Index: 31
Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 gene
Clinical Genetics
2021/6
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator
Nature
2021/4
