Neena B. Haider

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate

Neena B. Haider, Samuel G. Jacobson, Artur V. Cideciyan et al. · Nature Genetics · 2000 · 497 citations

Ocular Disease, Developmental Biology, Signal Transduction +10

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4

Kirk Mykytyn, Terry A. Braun, Rivka Carmi et al. · Nature Genetics · 2001 · 268 citations

Obesity, Metabolic Syndrome, Metabolic Disorder +8

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

Neena B. Haider · Human Molecular Genetics · 2001 · 200 citations · Full text

Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome

Lihua Ying, Yitzhak Katz, Menachem Schlesinger et al. · The American Journal of Human Genetics · 1999 · 123 citations · Full text

Immunohematology, Urology, Mendelian Disorder +9

A Bedouin Kindred with Infantile Nephronophthisis Demonstrates Linkage to Chromosome 9 by Homozygosity Mapping

Neena B. Haider, Rivka Carmi, Hana Shalev et al. · The American Journal of Human Genetics · 1998 · 87 citations · Full text

Bedouin Kindred, Homozygosity Mapping, Cytogenetics +12