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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
Am J Hum Genet. 2017 Nov 2;101(5):768-788. doi: 10.1016/j.ajhg.2017.10.003.
Am J Hum Genet. 2017.
PMID: 29100089
Free PMC article.
Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy.
Assia Batzir N, Kishor Bhagwat P, Larson A, Coban Akdemir Z, Bagłaj M, Bofferding L, Bosanko KB, Bouassida S, Callewaert B, Cannon A, Enchautegui Colon Y, Garnica AD, Harr MH, Heck S, Hurst ACE, Jhangiani SN, Isidor B, Littlejohn RO, Liu P, Magoulas P, Mar Fan H, Marom R, McLean S, Nezarati MM, Nugent KM, Petersen MB, Rocha ML, Roeder E, Smigiel R, Tully I, Weisfeld-Adams J, Wells KO; Baylor-Hopkins Center for Mendelian Genomics; Posey JE, Lupski JR, Beaudet AL, Wangler MF.
Assia Batzir N, et al. Among authors: bosanko kb.
Hum Mutat. 2020 Mar;41(3):641-654. doi: 10.1002/humu.23960. Epub 2019 Dec 19.
Hum Mutat. 2020.
PMID: 31769566
Free PMC article.
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An infant with ash-leaf and café au lait spots: a case of double phakomatosis.
Samanta D, Bosanko KB, Zarate YA.
Samanta D, et al. Among authors: bosanko kb.
Acta Neurol Belg. 2017 Mar;117(1):323-324. doi: 10.1007/s13760-016-0638-x. Epub 2016 Apr 4.
Acta Neurol Belg. 2017.
PMID: 27043227
No abstract available.
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Genetic counseling graduate training to address religion and spirituality in clinical practice: A qualitative exploration of programs in North America.
Murray A, Warren NS, Bosanko K, Williamson Dean L.
Murray A, et al.
J Genet Couns. 2020 Dec;29(6):1245-1258. doi: 10.1002/jgc4.1289. Epub 2020 May 30.
J Genet Couns. 2020.
PMID: 32472736
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