Stergachis A - Search Results

1

Development and evaluation of a continuous quality improvement programme for antimicrobial stewardship in six hospitals in Uganda.

Kiggundu R, Waswa JP, Nakambale HN, Kakooza F, Kassuja H, Murungi M, Akello H, Morries S, Joshi MP, Stergachis A, Konduri N. Kiggundu R, et al. Among authors: stergachis a. BMJ Open Qual. 2023 Jun;12(2):e002293. doi: 10.1136/bmjoq-2023-002293. BMJ Open Qual. 2023. PMID: 37336576 Free PMC article.

2

Effect of tenofovir containing ART on renal function in patients with moderate/severe reduced creatinine clearance at baseline: A retrospective study at two referral hospitals in Namibia.

Kalemeera F, Godman B, Stergachis A, Rennie T. Kalemeera F, et al. Among authors: stergachis a. Pharmacol Res Perspect. 2023 Feb;11(1):e00681. doi: 10.1002/prp2.681. Pharmacol Res Perspect. 2023. PMID: 36585791 Free PMC article.

3

STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179.

Grasberger H, Dumitrescu AM, Liao XH, Swanson EG, Weiss RE, Srichomkwun P, Pappa T, Chen J, Yoshimura T, Hoffmann P, França MM, Tagett R, Onigata K, Costagliola S, Ranchalis J, Vollger MR, Stergachis AB, Chong JX, Bamshad MJ, Smits G, Vassart G, Refetoff S. Grasberger H, et al. Among authors: stergachis ab. Nat Genet. 2024 May 7. doi: 10.1038/s41588-024-01717-7. Online ahead of print. Nat Genet. 2024. PMID: 38714869

4

Global burden associated with 85 pathogens in 2019: a systematic analysis for the Global Burden of Disease Study 2019.

IHME Pathogen Core Group. IHME Pathogen Core Group. Lancet Infect Dis. 2024 Apr 16:S1473-3099(24)00158-0. doi: 10.1016/S1473-3099(24)00158-0. Online ahead of print. Lancet Infect Dis. 2024. PMID: 38640940 Free article.

5

Global, regional, and national incidence and mortality burden of non-COVID-19 lower respiratory infections and aetiologies, 1990-2021: a systematic analysis from the Global Burden of Disease Study 2021.

GBD 2021 Lower Respiratory Infections and Antimicrobial Resistance Collaborators. GBD 2021 Lower Respiratory Infections and Antimicrobial Resistance Collaborators. Lancet Infect Dis. 2024 Apr 15:S1473-3099(24)00176-2. doi: 10.1016/S1473-3099(24)00176-2. Online ahead of print. Lancet Infect Dis. 2024. PMID: 38636536 Free article.

6

Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant.

Ezell KM, Tinker RJ, Furuta Y, Gulsevin A, Bastarache L, Hamid R, Cogan JD, Rives L, Neumann S, Corner B, Kozuria M, Phillips JA 3rd; Undiagnosed Diseases Network. Ezell KM, et al. Am J Med Genet A. 2024 Mar 21:e63597. doi: 10.1002/ajmg.a.63597. Online ahead of print. Am J Med Genet A. 2024. PMID: 38511854

7

Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism.

Dohrn MF, Bademci G, Rebelo AP, Jeanne M, Borja NA, Beijer D, Danzi MC, Bivona SA, Gueguen P, Zafeer MF; Undiagnosed Diseases Network; Tekin M, Züchner S. Dohrn MF, et al. Ann Clin Transl Neurol. 2024 Apr;11(4):1075-1079. doi: 10.1002/acn3.51963. Epub 2024 Mar 19. Ann Clin Transl Neurol. 2024. PMID: 38504481 Free PMC article.

8

Maternal and perinatal health research during emerging and ongoing epidemic threats: a landscape analysis and expert consultation.

Bonet M, Babinska M, Buekens P, Goudar SS, Kampmann B, Knight M, Meaney-Delman D, Lamprianou S, Rivas FM, Stergachis A, Toscano CM, Bhatia J, Chamberlain S, Chaudhry U, Mills J, Serazin E, Short H, Steene A, Wahlen M, Oladapo OT. Bonet M, et al. Among authors: stergachis a. BMJ Glob Health. 2024 Mar 7;9(3):e014393. doi: 10.1136/bmjgh-2023-014393. BMJ Glob Health. 2024. PMID: 38453249 Free PMC article.

9

Functional categorization of gene regulatory variants that cause Mendelian conditions.

Cheng YHH, Bohaczuk SC, Stergachis AB. Cheng YHH, et al. Among authors: stergachis ab. Hum Genet. 2024 Apr;143(4):559-605. doi: 10.1007/s00439-023-02639-w. Epub 2024 Mar 4. Hum Genet. 2024. PMID: 38436667 Free PMC article. Review.

10

Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis.

Pucel J, Briere LC, Reuter C, Gochyyev P; Undiagnosed Diseases Network; LeBlanc K. Pucel J, et al. Genet Med. 2024 Mar 1;26(6):101115. doi: 10.1016/j.gim.2024.101115. Online ahead of print. Genet Med. 2024. PMID: 38436216

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