Lorraine Mehltretter

Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics

Marcy C. Speer, David S. Enterline, Lorraine Mehltretter et al. · Journal of Genetic Counseling · 2003 · 238 citations · Full text

Medicine, Neurological Surgery, Neurosurgery +17

Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions

Abee L. Boyles, Ashley V. Billups, Kristen Deak et al. · Environmental Health Perspectives · 2006 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Phenotypic definition of Chiari type I malformation coupled with high‐density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15

Abee L. Boyles, David S. Enterline, Preston Hammock et al. · American Journal of Medical Genetics Part A · 2006 · 102 citations

Life Sciences, Genetics, Molecular Genetics +16

Analysis ofALDH1A2,CYP26A1,CYP26B1,CRABP1, andCRABP2 in human neural tube defects suggests a possible association with alleles inALDH1A2

Kristen Deak, Margaret E. Dickerson, Elwood Linney et al. · Birth Defects Research Part A Clinical and Molecular Teratology · 2005 · 81 citations · Full text

Life Sciences, Developmental Biology, Genetics +15

Recurrence risks for neural tube defects in siblings of patients with lipomyelomeningocele

Courtney Sebold, Elizabeth C. Melvin, Debbie Siegel et al. · Genetics in Medicine · 2005 · 46 citations · Full text

Medicine, Pediatrics, Human Genetics +10