Saghira Malik Sharif

Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report

Hanan Hamamy, Stylianos E. Antonarakis, Luigi Luca Cavalli-Sforza et al. · Genetics in Medicine · 2011 · 333 citations · Full text

Intimate Relationship, Gender Studies, Sociology +8

The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat

Ursula M. Smith, Mark Consugar, Louise Tee et al. · Nature Genetics · 2006 · 289 citations

Signal Transduction, Developmental Biology, Transmembrane Protein Meckelin +5

Quantification of Homozygosity in Consanguineous Individuals with Autosomal Recessive Disease

C. Geoffrey Woods, James J. Cox, Kelly Springell et al. · The American Journal of Human Genetics · 2006 · 264 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +9

Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome

C. Geoffrey Woods, Sigmar Stricker, Petra Seemann et al. · The American Journal of Human Genetics · 2006 · 158 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +9

Human ASPM participates in spindle organisation, spindle orientation and cytokinesis

J. William Higgins, Carol Midgley, Anna-Maria Bergh et al. · BMC Cell Biology · 2010 · 125 citations · Full text