Weaver M - Search Results

1

Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies.

Stephens K, Weaver M, Leppig KA, Maruyama K, Emanuel PD, Le Beau MM, Shannon KM. Stephens K, et al. Among authors: weaver m. Blood. 2006 Sep 1;108(5):1684-9. doi: 10.1182/blood-2005-11-011486. Epub 2006 May 11. Blood. 2006. PMID: 16690971 Free PMC article.

2

Evidence that juvenile myelomonocytic leukemia can arise from a pluripotential stem cell.

Cooper LJ, Shannon KM, Loken MR, Weaver M, Stephens K, Sievers EL. Cooper LJ, et al. Among authors: weaver m. Blood. 2000 Sep 15;96(6):2310-3. Blood. 2000. PMID: 10979983 Free article.

3

Patterns of hematopoietic lineage involvement in children with neurofibromatosis type 1 and malignant myeloid disorders.

Miles DK, Freedman MH, Stephens K, Pallavicini M, Sievers EL, Weaver M, Grunberger T, Thompson P, Shannon KM. Miles DK, et al. Among authors: weaver m. Blood. 1996 Dec 1;88(11):4314-20. Blood. 1996. PMID: 8943868 Free article.

4

Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromata.

Leppig KA, Kaplan P, Viskochil D, Weaver M, Ortenberg J, Stephens K. Leppig KA, et al. Among authors: weaver m. Am J Med Genet. 1997 Dec 12;73(2):197-204. doi: 10.1002/(sici)1096-8628(1997)73:2<197::aid-ajmg17>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9409873

5

NF1 microdeletion breakpoints are clustered at flanking repetitive sequences.

Dorschner MO, Sybert VP, Weaver M, Pletcher BA, Stephens K. Dorschner MO, et al. Among authors: weaver m. Hum Mol Genet. 2000 Jan 1;9(1):35-46. doi: 10.1093/hmg/9.1.35. Hum Mol Genet. 2000. PMID: 10587576

6

Refined mapping of the human serotonin transporter (SLC6A4) gene within 17q11 adjacent to the CPD and NF1 genes.

Shen S, Battersby S, Weaver M, Clark E, Stephens K, Harmar AJ. Shen S, et al. Among authors: weaver m. Eur J Hum Genet. 2000 Jan;8(1):75-8. doi: 10.1038/sj.ejhg.5200400. Eur J Hum Genet. 2000. PMID: 10713891

7

Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patients.

Stephens K, Ehrlich P, Weaver M, Le R, Spencer A, Sybert VP. Stephens K, et al. Among authors: weaver m. J Invest Dermatol. 1997 Mar;108(3):349-53. doi: 10.1111/1523-1747.ep12286486. J Invest Dermatol. 1997. PMID: 9036937 Free article.

8

Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.

Sybert VP, Francis JS, Corden LD, Smith LT, Weaver M, Stephens K, McLean WH. Sybert VP, et al. Among authors: weaver m. Am J Hum Genet. 1999 Mar;64(3):732-8. doi: 10.1086/302278. Am J Hum Genet. 1999. PMID: 10053007 Free PMC article.

9

Consistent direction despite wavering policy: reductions in resident physician extended duration shifts over 20 years.

Weaver MD, Barger LK, Sullivan JP, Qadri S, Czeisler CA, Landrigan CP. Weaver MD, et al. Am J Med. 2025 Jan 16:S0002-9343(25)00005-1. doi: 10.1016/j.amjmed.2025.01.001. Online ahead of print. Am J Med. 2025. PMID: 39826572

10

Detection, quantification, and characterization of airborne Aspergillus flavus within the corn canopy.

Weaver MA, Park LC, Brewer MJ, Grodowitz MJ, Abbas HK. Weaver MA, et al. Mycotoxin Res. 2025 Jan 14. doi: 10.1007/s12550-025-00581-6. Online ahead of print. Mycotoxin Res. 2025. PMID: 39808409

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