BCL11B-related disorder in two canadian children: Expanding the clinical phenotype

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

Sue Richards, Nazneen Aziz, Sherri J. Bale et al. · Genetics in Medicine · 2015 · 32.2K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Analysis of protein-coding genetic variation in 60,706 humans

Monkol Lek, Konrad J. Karczewski, Eric Vallabh Minikel et al. · Nature · 2016 · 10.3K citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The BCL11 gene family: involvement of BCL11A in lymphoid malignancies

Ed Satterwhite, Takashi Sonoki, Tony G. Willis et al. · Blood · 2001 · 313 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription

Cristina Dias, Sara B. Estruch, Sarah A. Graham et al. · The American Journal of Human Genetics · 2016 · 164 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype

Christian Brendel, Swaroopa Guda, Raffaele Renella et al. · Journal of Clinical Investigation · 2016 · 161 citations · Full text

Life Sciences, Genetics, Hematology +15