Heidemarie Neitzel
Publications by Year
Research Areas
Chromosomal and Genetic Variations, Genomic variations and chromosomal abnormalities, DNA Repair Mechanisms, Prenatal Screening and Diagnostics, Genomics and Chromatin Dynamics
Most-Cited Works
- → A routine method for the establishment of permanent growing lymphoblastoid cell lines(1986)644 cited
- → Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer(2006)641 cited
- → DNA Ligase IV Mutations Identified in Patients Exhibiting Developmental Delay and Immunodeficiency(2001)537 cited
- → Establishment and Characterization of an Immortalized Human Sebaceous Gland Cell Line (SZ95)1(1999)353 cited
- → Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation(2004)266 cited
- → Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1)(2003)171 cited
- → Regulation of mitotic entry by microcephalin and its overlap with ATR signalling(2006)165 cited
- → Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition(2002)159 cited
- → Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12(1996)145 cited
- → Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor(2003)138 cited