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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 1
2015 2
2016 5
2017 5
2018 3
2019 3
2020 6
2021 7
2022 9
2023 6

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37 results

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Page 1
Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.
Cummings BB, Marshall JL, Tukiainen T, Lek M, Donkervoort S, Foley AR, Bolduc V, Waddell LB, Sandaradura SA, O'Grady GL, Estrella E, Reddy HM, Zhao F, Weisburd B, Karczewski KJ, O'Donnell-Luria AH, Birnbaum D, Sarkozy A, Hu Y, Gonorazky H, Claeys K, Joshi H, Bournazos A, Oates EC, Ghaoui R, Davis MR, Laing NG, Topf A; Genotype-Tissue Expression Consortium; Kang PB, Beggs AH, North KN, Straub V, Dowling JJ, Muntoni F, Clarke NF, Cooper ST, Bönnemann CG, MacArthur DG. Cummings BB, et al. Among authors: gonorazky h. Sci Transl Med. 2017 Apr 19;9(386):eaal5209. doi: 10.1126/scitranslmed.aal5209. Sci Transl Med. 2017. PMID: 28424332 Free PMC article.
Newborn Screening for Spinal Muscular Atrophy: Ontario Testing and Follow-up Recommendations.
McMillan HJ, Kernohan KD, Yeh E, Amburgey K, Boyd J, Campbell C, Dowling JJ, Gonorazky H, Marcadier J, Tarnopolsky MA, Vajsar J, MacKenzie A, Chakraborty P. McMillan HJ, et al. Among authors: gonorazky h. Can J Neurol Sci. 2021 Jul;48(4):504-511. doi: 10.1017/cjn.2020.229. Epub 2020 Oct 16. Can J Neurol Sci. 2021. PMID: 33059774 Clinical Trial.
Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease.
Gonorazky HD, Naumenko S, Ramani AK, Nelakuditi V, Mashouri P, Wang P, Kao D, Ohri K, Viththiyapaskaran S, Tarnopolsky MA, Mathews KD, Moore SA, Osorio AN, Villanova D, Kemaladewi DU, Cohn RD, Brudno M, Dowling JJ. Gonorazky HD, et al. Am J Hum Genet. 2019 Mar 7;104(3):466-483. doi: 10.1016/j.ajhg.2019.01.012. Epub 2019 Feb 28. Am J Hum Genet. 2019. PMID: 30827497 Free PMC article.
The genetics of congenital myopathies.
Gonorazky HD, Bönnemann CG, Dowling JJ. Gonorazky HD, et al. Handb Clin Neurol. 2018;148:549-564. doi: 10.1016/B978-0-444-64076-5.00036-3. Handb Clin Neurol. 2018. PMID: 29478600 Review.
Signs and Symptoms in Congenital Myopathies.
Gonorazky HD, Dowling JJ, Volpatti JR, Vajsar J. Gonorazky HD, et al. Semin Pediatr Neurol. 2019 Apr;29:3-11. doi: 10.1016/j.spen.2019.01.002. Epub 2019 Jan 16. Semin Pediatr Neurol. 2019. PMID: 31060723 Review.
CAMK4-related Case of Hyperkinetic Movement Disorder.
Alawneh I, Amburgey K, Gonorazky H, Gorodetsky C. Alawneh I, et al. Among authors: gonorazky h. Mov Disord Clin Pract. 2023 Mar 3;10(4):707-709. doi: 10.1002/mdc3.13702. eCollection 2023 Apr. Mov Disord Clin Pract. 2023. PMID: 37070062 No abstract available.
Ontario Newborn Screening for Spinal Muscular Atrophy: The First Year.
Kernohan KD, McMillan HJ, Yeh E, Lacaria M, Kowalski M, Campbell C, Dowling JJ, Gonorazky H, Marcadier J, Tarnopolsky MA, Vajsar J, Mackenzie A, Chakraborty P. Kernohan KD, et al. Among authors: gonorazky h. Can J Neurol Sci. 2022 Nov;49(6):821-823. doi: 10.1017/cjn.2021.231. Epub 2021 Oct 8. Can J Neurol Sci. 2022. PMID: 34620260 No abstract available.
Natural history of a mouse model of X-linked myotubular myopathy.
Sarikaya E, Sabha N, Volpatti J, Pannia E, Maani N, Gonorazky HD, Celik A, Liang Y, Onofre-Oliveira P, Dowling JJ. Sarikaya E, et al. Among authors: gonorazky hd. Dis Model Mech. 2022 Jul 1;15(7):dmm049342. doi: 10.1242/dmm.049342. Epub 2022 Jul 25. Dis Model Mech. 2022. PMID: 35694952 Free PMC article.
Child Neurology: RNA Sequencing for the Diagnosis of Lissencephaly.
Qashqari H, Ramani A, Gonorazky H, Amburgey K, Ghahramani Seno MM, Brudno M, Naumenko S, Das S, Dowling JJ. Qashqari H, et al. Among authors: gonorazky h. Neurology. 2021 May 20;97(12):e1253-6. doi: 10.1212/WNL.0000000000012265. Online ahead of print. Neurology. 2021. PMID: 34016710 Free PMC article. No abstract available.
37 results