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A human MAP kinase interactome.
Bandyopadhyay S, Chiang CY, Srivastava J, Gersten M, White S, Bell R, Kurschner C, Martin C, Smoot M, Sahasrabudhe S, Barber DL, Chanda SK, Ideker T. Bandyopadhyay S, et al. Among authors: white s. Nat Methods. 2010 Oct;7(10):801-5. doi: 10.1038/nmeth.1506. Nat Methods. 2010. PMID: 20936779 Free PMC article.
Genome-scale functional profiling of the mammalian AP-1 signaling pathway.
Chanda SK, White S, Orth AP, Reisdorph R, Miraglia L, Thomas RS, DeJesus P, Mason DE, Huang Q, Vega R, Yu DH, Nelson CG, Smith BM, Terry R, Linford AS, Yu Y, Chirn GW, Song C, Labow MA, Cohen D, King FJ, Peters EC, Schultz PG, Vogt PK, Hogenesch JB, Caldwell JS. Chanda SK, et al. Among authors: white s. Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12153-8. doi: 10.1073/pnas.1934839100. Epub 2003 Sep 26. Proc Natl Acad Sci U S A. 2003. PMID: 14514886 Free PMC article.
Biomarkers.
Liebscher M, White S, Touron E, Mézenge F, Chocat A, Coulbaut L, Vivien D, la Sayette V, Marchant NL, Chételat G, Klimecki OM, Poisnel G, Wirth M; Medit‐Ageing Research Group. Liebscher M, et al. Among authors: white s. Alzheimers Dement. 2024 Dec;20 Suppl 2:e088827. doi: 10.1002/alz.088827. Alzheimers Dement. 2024. PMID: 39785588
Public Health.
Key MN, White S, Zweydoff R, Hawes T, Billinger SA, Szabo-Reed A, Vidoni ED. Key MN, et al. Among authors: white s. Alzheimers Dement. 2024 Dec;20 Suppl 7:e093192. doi: 10.1002/alz.093192. Alzheimers Dement. 2024. PMID: 39784648
Biomarkers.
Parker TD, Bethlehem RAI, Seidlitz J, White SR, Dorfschmidt L, Bernstock JD, Bourke N, David MC, de Taurines AFLG, Giovane MD, Graham NS, Kolanko MA, Zimmerman KA, Malhotra P, Patel M, Scott GP, Alexander-Bloch A, Bullmore ET, Sharp DJ. Parker TD, et al. Among authors: white sr. Alzheimers Dement. 2024 Dec;20 Suppl 2:e086445. doi: 10.1002/alz.086445. Alzheimers Dement. 2024. PMID: 39784424
A blended learning approach for capacity strengthening to improve the quality of integrated HIV, TB, and malaria services during antenatal and postnatal care in LMICs: a feasibility study.
Ladur AN, Egere U, Ravit M, Mgawadere F, Murray C, White SA, Hauwa M, Mutai R, Nyaga L, Duncan S, Bashir I, Ayinde OO, Bakar R, Katalambula L, Federici C, Torbica A, Furtado N, Kumah EA, Ameh C. Ladur AN, et al. Among authors: white sa. BMC Med Educ. 2025 Jan 8;25(1):35. doi: 10.1186/s12909-024-06633-2. BMC Med Educ. 2025. PMID: 39780210 Free article.
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases.
Stenton SL, Laricchia K, Lake NJ, Chaluvadi S, Ganesh V, DiTroia S, Osei-Owusu I, Pais L, O'Heir E, Austin-Tse C, O'Leary M, Abu Shanap M, Barrows C, Berger S, Bönnemann CG, Bujakowska KM, Campagna DR, Compton AG, Donkervoort S, Fleming MD, Gallacher L, Gleeson JG, Haliloglu G, Pierce EA, Place EM, Sankaran VG, Shimamura A, Stark Z, Yang Tan T, Thorburn DR, White SM; Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium; Vilain E, Lek M, Rehm HL, O'Donnell-Luria A. Stenton SL, et al. Among authors: white sm. medRxiv [Preprint]. 2024 Dec 26:2024.12.22.24319370. doi: 10.1101/2024.12.22.24319370. medRxiv. 2024. PMID: 39763565 Free PMC article. Preprint.
6,487 results