Yasmin Raashid

An SCN9A channelopathy causes congenital inability to experience pain

James J. Cox, Frank Reimann, Adeline K. Nicholas et al. · Nature · 2006 · 1.6K citations · Full text

Life Sciences, Neurobiology, Neuroscience +11

Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

Manir Ali, Martin McKibbin, Adam Booth et al. · The American Journal of Human Genetics · 2009 · 325 citations · Full text

Medicine, Genetics, Ophthalmology +12

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

Kamron N. Khan, Clare V. Logan, Martin McKibbin et al. · Human Molecular Genetics · 2011 · 95 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

Kamron N. Khan, Adam K Rudkin, David Parry et al. · The American Journal of Human Genetics · 2011 · 81 citations · Full text

Medicine, Genetics, Ophthalmology +17

‘All is done by Allah’. Understandings of Down syndrome and prenatal testing in Pakistan

Louise Bryant, Shenaz Ahmed, Mushtaq Ahmed et al. · Social Science & Medicine · 2011 · 61 citations

Medicine, Maternal Health, Obstetrics +16