Tammy Kammin

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L. Collins et al. · Nature Genetics · 2016 · 346 citations · Full text

Human Congenital Anomalies, Developmental Anomaly, Developmental Biology +8

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Natalie D. Shaw, Harrison Brand, Zachary A Kupchinsky et al. · Nature Genetics · 2017 · 160 citations · Full text

Rare Diseases, Smchd1 Mutations, Mendelian Disorder +9

SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility

Samantha L.P. Schilit, Shreya Menon, Corinna Friedrich et al. · The American Journal of Human Genetics · 2019 · 96 citations · Full text

Infertility, Andrology, Fertility +10

Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis

Zehra Ordulu, Tammy Kammin, Harrison Brand et al. · The American Journal of Human Genetics · 2016 · 95 citations · Full text

Chromatin, Dna Sequencing, Dna +13

Actin capping protein CAPZB regulates cell morphology, differentiation, and neural crest migration in craniofacial morphogenesis

Kusumika Mukherjee, Kana Ishii, Vamsee Pillalamarri et al. · Human Molecular Genetics · 2016 · 55 citations · Full text

Neural Crest Cells, Maxillofacial Growth, Cytoskeleton +19