Olaf A Bodamer (Olaf Bodamer)

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 10

Top Topics

Muscular Dystrophy

Intellectual Disability

Top Venues

American journal of medical genetics. Part A

Molecular genetics & genomic medicine

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

Publications

Suraj S Shah, Anne Fulton, Mireille Jabroun, Diana Brightman, Brittany N Simpson, Olaf A Bodamer
Insights into the genotype-phenotype relationship of ocular manifestations in Kabuki syndrome. American journal of medical genetics. Part A (2023)
Kelly K Barry, Michaelangelo Tsaparlis, Deborah Hoffman, Deborah Hartman, Margaret P Adam, Christina Hung, Olaf A Bodamer
From Genotype to Phenotype-A Review of Kabuki Syndrome. Genes 13 (10) (2022)
Rachel T Stadelmaier, Margaret A Kenna, Devon Barrett, Thomas E Mullen, Olaf A Bodamer, Pankaj B Agrawal, Caroline D Robson, Monica Hsiung Wojcik
Neuroimaging in Kabuki syndrome and another KMT2D-related disorder. American journal of medical genetics. Part A 185 (12) (2021)
Aya Abu-El-Haija, Caroline McGowan, Deborah Vanderveen, Olaf A Bodamer
Autosomal-dominant WFS1-related disorder-Report of a novel WFS1 variant and review of the phenotypic spectrum of autosomal recessive and dominant forms. American journal of medical genetics. Part A 185 (2) (2020)
Suraj S Shah, Asma Rashid, Olaf A Bodamer
Congenital microgastria-limb reduction association: A case report and review of the literature. American journal of medical genetics. Part A 182 (12) (2020)
Christina Y Hung, Mario Rodriguez, Abra Roberts, Mislen Bauer, Ivana Mihalek, Olaf A Bodamer
A novel FAM20C mutation causes a rare form of neonatal lethal Raine syndrome. American journal of medical genetics. Part A 179 (9) (2019)
Chen E Rosenberg, Tara Daly, Christina Hung, Irene Hsueh, Andrew W Lindsley, Olaf A Bodamer
Prenatal and perinatal history in Kabuki Syndrome. American journal of medical genetics. Part A 182 (1) (2019)
Yirou Wang, Niu Li, Zhe Su, Yufei Xu, Shijian Liu, Yao Chen, Xin Li, Yiping Shen, Christina Hung, Jian Wang, Xiumin Wang, Olaf A Bodamer
The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series. American journal of medical genetics. Part A 182 (4) (2019)
Teresa Romeo Luperchio, Carolyn D Applegate, Olaf A Bodamer, Hans Tomas Bjornsson
Haploinsufficiency of KMT2D is sufficient to cause Kabuki syndrome and is compatible with life. Molecular genetics & genomic medicine 8 (2) (2019)
Tara Daly, Abra Roberts, Edward Yang, Ganeshwaran H Mochida, Olaf A Bodamer
Holoprosencephaly in Kabuki syndrome. American journal of medical genetics. Part A 182 (3) (2019)