Weiss S - Search Results

1

Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry.

Ben Yosef T, Banin E, Chervinsky E, Shalev SA, Leibu R, Mezer E, Rotenstreich Y, Goldenberg-Cohen N, Weiss S, Khan MI, Panneman DM, Hitti-Malin RJ, Weiner C, Roosing S, Cremers FPM, Pras E, Zur D, Newman H, Deitch I, Sharon D, Ehrenberg M. Ben Yosef T, et al. Among authors: weiss s. Mol Vis. 2023 Apr 22;29:1-12. eCollection 2023. Mol Vis. 2023. PMID: 37287645 Free PMC article.

2

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population.

Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B. Baldwin CT, et al. Among authors: weiss s. Hum Mol Genet. 1995 Sep;4(9):1637-42. doi: 10.1093/hmg/4.9.1637. Hum Mol Genet. 1995. PMID: 8541853

3

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, Blumenfeld A, Frydman M, Friedman TB, King MC, Avraham KB. Vahava O, et al. Among authors: weiss s. Science. 1998 Mar 20;279(5358):1950-4. doi: 10.1126/science.279.5358.1950. Science. 1998. PMID: 9506947

4

Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor.

Frydman M, Vreugde S, Nageris BI, Weiss S, Vahava O, Avraham KB. Frydman M, et al. Among authors: weiss s. Arch Otolaryngol Head Neck Surg. 2000 May;126(5):633-7. doi: 10.1001/archotol.126.5.633. Arch Otolaryngol Head Neck Surg. 2000. PMID: 10807331

5

Genetic mapping of the gene for Usher syndrome: linkage analysis in a large Samaritan kindred.

Bonné-Tamir B, Korostishevsky M, Kalinsky H, Seroussi E, Beker R, Weiss S, Godel V. Bonné-Tamir B, et al. Among authors: weiss s. Genomics. 1994 Mar 1;20(1):36-42. doi: 10.1006/geno.1994.1124. Genomics. 1994. PMID: 8020954

6

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Bonné-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA. Bonné-Tamir B, et al. Among authors: weiss s. Am J Hum Genet. 1996 Jun;58(6):1254-9. Am J Hum Genet. 1996. PMID: 8651303 Free PMC article.

7

Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.

Iyengar S, Kalinsky H, Weiss S, Korostishevsky M, Sadeh M, Zhao Y, Kidd KK, Bonne-Tamir B. Iyengar S, et al. Among authors: weiss s. J Med Genet. 1997 May;34(5):391-4. doi: 10.1136/jmg.34.5.391. J Med Genet. 1997. PMID: 9152836 Free PMC article.

8

Interferon signaling in the nasal epithelium distinguishes among lethal and common cold coronaviruses and mediates viral clearance.

Otter CJ, Renner DM, Fausto A, Tan LH, Cohen NA, Weiss SR. Otter CJ, et al. Among authors: weiss sr. Proc Natl Acad Sci U S A. 2024 May 21;121(21):e2402540121. doi: 10.1073/pnas.2402540121. Epub 2024 May 17. Proc Natl Acad Sci U S A. 2024. PMID: 38758698

9

To plan efficacious epilepsy surgery.

Weiss SA, Sperling MR, Engel J Jr, Staba R. Weiss SA, et al. Brain. 2024 May 17:awae162. doi: 10.1093/brain/awae162. Online ahead of print. Brain. 2024. PMID: 38758083 No abstract available.

10

The aged tumor microenvironment limits T cell control of cancer.

Chen ACY, Jaiswal S, Martinez D, Yerinde C, Ji K, Miranda V, Fung ME, Weiss SA, Zschummel M, Taguchi K, Garris CS, Mempel TR, Hacohen N, Sen DR. Chen ACY, et al. Among authors: weiss sa. Nat Immunol. 2024 May 14. doi: 10.1038/s41590-024-01828-7. Online ahead of print. Nat Immunol. 2024. PMID: 38745085

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