Ladd S - Search Results

1

Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature.

Dukes-Rimsky L, Guzauskas GF, Holden KR, Griggs R, Ladd S, Montoya Mdel C, DuPont BR, Srivastava AK. Dukes-Rimsky L, et al. Among authors: ladd s. Am J Med Genet A. 2011 Sep;155A(9):2146-53. doi: 10.1002/ajmg.a.34137. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834054 Free PMC article.

2

Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities.

Griggs BL, Ladd S, Saul RA, DuPont BR, Srivastava AK. Griggs BL, et al. Among authors: ladd s. Genomics. 2008 Feb;91(2):195-202. doi: 10.1016/j.ygeno.2007.10.011. Epub 2007 Dec 3. Genomics. 2008. PMID: 18060736 Free PMC article.

3

Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus.

Griggs BL, Ladd S, Decker A, DuPont BR, Asamoah A, Srivastava AK. Griggs BL, et al. Among authors: ladd s. Eur J Hum Genet. 2009 Jan;17(1):30-6. doi: 10.1038/ejhg.2008.183. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854857 Free PMC article.

4

Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability.

Bhalla K, Luo Y, Buchan T, Beachem MA, Guzauskas GF, Ladd S, Bratcher SJ, Schroer RJ, Balsamo J, DuPont BR, Lilien J, Srivastava AK. Bhalla K, et al. Among authors: ladd s. Am J Hum Genet. 2008 Dec;83(6):703-13. doi: 10.1016/j.ajhg.2008.10.020. Epub 2008 Nov 13. Am J Hum Genet. 2008. PMID: 19012874 Free PMC article.

5

Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22.3.

Rodriguez JD, Bhat SS, Meloni I, Ladd S, Leslie ND, Doyne EO, Renieri A, Dupont BR, Stevenson RE, Schwartz CE, Srivastava AK. Rodriguez JD, et al. Among authors: ladd s. Am J Med Genet A. 2010 Mar;152A(3):713-7. doi: 10.1002/ajmg.a.33208. Am J Med Genet A. 2010. PMID: 20186809

6

Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies.

Bhat SS, Schmidt KR, Ladd S, Kim KC, Schwartz CE, Simensen RJ, DuPont BR, Stevenson RE, Srivastava AK. Bhat SS, et al. Among authors: ladd s. Cytogenet Genome Res. 2006;112(1-2):170-5. doi: 10.1159/000087531. Cytogenet Genome Res. 2006. PMID: 16276108

7

AGTR2 mutations in X-linked mental retardation.

Vervoort VS, Beachem MA, Edwards PS, Ladd S, Miller KE, de Mollerat X, Clarkson K, DuPont B, Schwartz CE, Stevenson RE, Boyd E, Srivastava AK. Vervoort VS, et al. Among authors: ladd s. Science. 2002 Jun 28;296(5577):2401-3. doi: 10.1126/science.1072191. Science. 2002. PMID: 12089445

8

Disruption of the IL1RAPL1 gene associated with a pericentromeric inversion of the X chromosome in a patient with mental retardation and autism.

Bhat SS, Ladd S, Grass F, Spence JE, Brasington CK, Simensen RJ, Schwartz CE, Dupont BR, Stevenson RE, Srivastava AK. Bhat SS, et al. Among authors: ladd s. Clin Genet. 2008 Jan;73(1):94-6. doi: 10.1111/j.1399-0004.2007.00920.x. Epub 2007 Nov 14. Clin Genet. 2008. PMID: 18005360 No abstract available.

9

Distinct Type 1 Immune Networks Underlie the Severity of Restrictive Lung Disease after COVID-19.

Canderan G, Muehling LM, Kadl A, Ladd S, Bonham C, Cross CE, Lima SM, Yin X, Sturek JM, Wilson JM, Keshavarz B, Bryant N, Murphy DD, Cheon IS, McNamara CA, Sun J, Utz PJ, Dolatshahi S, Irish JM, Woodfolk JA. Canderan G, et al. Among authors: ladd s. bioRxiv [Preprint]. 2024 Apr 4:2024.04.03.587929. doi: 10.1101/2024.04.03.587929. bioRxiv. 2024. PMID: 38617217 Free PMC article. Preprint.

10

The mobilization and transport of newly fixed carbon are driven by plant water use in an experimental rainforest under drought.

Huang J, Ladd SN, Ingrisch J, Kübert A, Meredith LK, van Haren J, Bamberger I, Daber LE, Kühnhammer K, Bailey K, Hu J, Fudyma J, Shi L, Dippold MA, Meeran K, Miller L, O'Brien MJ, Yang H, Herrera-Ramírez D, Hartmann H, Trumbore S, Bahn M, Werner C, Lehmann MM. Huang J, et al. Among authors: ladd sn. J Exp Bot. 2024 Apr 15;75(8):2545-2557. doi: 10.1093/jxb/erae030. J Exp Bot. 2024. PMID: 38271585

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