Setareh Sadat Banihosseini

Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pedigree by 500 K SNP Arrays

Seyedmehdi Shojaee, Farzad Sina, Setareh Sadat Banihosseini et al. · The American Journal of Human Genetics · 2008 · 247 citations · Full text

K Snp Arrays, Genome-wide Linkage Analysis, Genetic Disorder +7

Homozygous Missense Mutation in Fibulin-5 in an Iranian Autosomal Recessive Cutis Laxa Pedigree and Associated Haplotype

Elahe Elahi, Reza Kalhor, Setareh Sadat Banihosseini et al. · Journal of Investigative Dermatology · 2006 · 59 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7

Four Mutations (Three Novel, One Founder) in<i>TACSTD2</i>among Iranian GDLD Patients

Afagh Alavi, Elahe Elahi, Mehdi Hosseini Tehrani et al. · Investigative Ophthalmology & Visual Science · 2007 · 24 citations

<i>PRKN</i>, <i>DJ‐1</i>, and <i>PINK1</i> screening identifies novel splice site mutation in <i>PRKN</i> and two novel <i>DJ‐1</i> mutations

Farzaneh Ghazavi, Zeinab Fazlali, Setareh Sadat Banihosseini et al. · Movement Disorders · 2010 · 18 citations

Variation in plasma leptin levels in young Iranian children with cystic fibrosis

Maryam Monajemzadeh, Mohammad Taghi Haghi Ashtıani, Ehsan Sadrian et al. · Archives of Medical Science · 2013 · 10 citations · Full text