Saul Merin

Comparative Genomics and Gene Expression Analysis Identifies BBS9, a New Bardet-Biedl Syndrome Gene

Darryl Nishimura, Ruth E. Swiderski, Charles Searby et al. · The American Journal of Human Genetics · 2005 · 212 citations · Full text

Engineering, Mendelian Disorder, Genetic Disorder +9

A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews

Lina Zelinger, Eyal Banin, Alexey Obolensky et al. · The American Journal of Human Genetics · 2011 · 138 citations · Full text

Mendelian Disorder, Genetic Disorder, Ashkenazi Jews +7

Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa

Dikla Bandah‐Rozenfeld, Liliana Mizrahi‐Meissonnier, Chen Farhy et al. · The American Journal of Human Genetics · 2010 · 103 citations · Full text

Engineering, Mendelian Disorder, Genetic Disorder +9

Schirmer Test and Break-Up Time of Tear Film in Normal Subjects

Amiram Shapiro, Saul Merin · American Journal of Ophthalmology · 1979 · 97 citations

Schirmer Test, Tear Film, Normal Subjects

Long-term assessment of combined vitamin A and E treatment for the prevention of retinal degeneration in abetalipoproteinaemia and hypobetalipo-proteinaemia patients

Itay Chowers, Eyal Banin, Saul Merin et al. · Eye · 2001 · 81 citations · Full text

Nutrition, Long-term Assessment, Ocular Disease +7