Mustafa Khokha
Affiliations: | Genetics | Yale Med Sch, New Haven, CT, United States |
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| MacColl Garfinkel A, Mnatsakanyan N, Patel JH, et al. (2023) Mitochondrial leak metabolism induces the Spemann-Mangold Organizer via Hif-1α in Xenopus. Developmental Cell |
| Khokha MK, Liu KJ, Wallingford JB. (2020) Challenges and opportunities at the interface of birth defects, human genetics and developmental biology. Development (Cambridge, England). 147 |
| Brodsky NN, Boyarchuk O, Kovalchuk T, et al. (2020) Novel compound heterozygous variants in NHLRC2 in a patient with FINCA syndrome. Journal of Human Genetics |
| Alharatani R, Ververi A, Beleza-Meireles A, et al. (2020) Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. Human Molecular Genetics |
| Duncan AR, González DP, Del Viso F, et al. (2019) Alkylglycerol monooxygenase, a heterotaxy candidate gene, regulates left-right patterning via Wnt signaling. Developmental Biology |
| Mitros T, Lyons JB, Session AM, et al. (2019) A chromosome-scale genome assembly and dense genetic map for Xenopus tropicalis. Developmental Biology |
| Griffin JN, Del Viso F, Duncan AR, et al. (2017) RAPGEF5 Regulates Nuclear Translocation of β-Catenin. Developmental Cell |
| Khokha MK, Mitchell LE, Wallingford JB. (2017) White paper on the study of birth defects. Birth Defects Research. 109: 180-185 |
| Khokha MK, Mitchell LE, Wallingford JB. (2016) An opportunity to address the genetic causes of birth defects. Pediatric Research |
| Endicott SJ, Basu B, Khokha M, et al. (2015) The NIMA-like kinase Nek2 is a key switch balancing cilia biogenesis and resorption in the development of left-right asymmetry. Development (Cambridge, England) |