Brenda Finucane

Mutations in RAI1 associated with Smith–Magenis syndrome

Rebecca E. Slager, Tiffany Lynn Newton, Christopher N. Vlangos et al. · Nature Genetics · 2003 · 357 citations · Full text

Mendelian Disorder, Smith–magenis Syndrome, Genetic Disorder +7

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: Cast a wide FISHing net!

Donna M. McDonald‐McGinn, Melissa K. Tonnesen, Ayala Laufer‐Cahana et al. · Genetics in Medicine · 2001 · 314 citations · Full text

Biology, Genotype-phenotype Association, Wide Fishing Net +6

Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia

Lars Feuk, Aino Kalervo, Marita Lipsanen‐Nyman et al. · The American Journal of Human Genetics · 2006 · 185 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +8

Genetic Counseling for Fragile X Syndrome: Updated Recommendations of the National Society of Genetic Counselors

Allyn McConkie‐Rosell, Brenda Finucane, Amy Cronister et al. · Journal of Genetic Counseling · 2005 · 160 citations · Full text

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission

Carolyn M. Yrigollen, Loreto Martorell, Blythe Durbin‐Johnson et al. · Journal of Neurodevelopmental Disorders · 2014 · 109 citations · Full text