Kwame Anyane‐Yeboa

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study

Slavé Petrovski, Vimla S. Aggarwal, Jessica L. Giordano et al. · The Lancet · 2019 · 590 citations

Developmental Anomaly, Sequencing, Whole-exome Sequencing +12

Molecular mechanism for duplication 17p11.2— the homologous recombination reciprocal of the Smith-Magenis microdeletion

Lorraine Potocki, Ken-Shiung Chen, Sung Sup Park et al. · Nature Genetics · 2000 · 422 citations · Full text

Genome Instability, Duplication 17P11.2—, Genetics +9

Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients

Christine Carlson, Howard I. Sirotkin, Raj K. Pandita et al. · The American Journal of Human Genetics · 1997 · 357 citations · Full text

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

The usefulness of whole-exome sequencing in routine clinical practice

Alejandro Iglesias, Kwame Anyane‐Yeboa, Julia Wynn et al. · Genetics in Medicine · 2014 · 237 citations · Full text

Bioinformatics, Long-read Sequencing, Medicine +8