Thompson K - Search Results

1

A primary genetic map of chromosome 13q.

Leppert M, Cavenee W, Callahan P, Holm T, O'Connell P, Thompson K, Lathrop GM, Lalouel JM, White R. Leppert M, et al. Among authors: thompson k. Am J Hum Genet. 1986 Oct;39(4):425-37. Am J Hum Genet. 1986. PMID: 3464200 Free PMC article.

2

Association of terminal chromosome 1 deletion with sertoli cell-only syndrome.

Hathout EH, Thompson K, Baum M, Dumars KW. Hathout EH, et al. Among authors: thompson k. Am J Med Genet. 1998 Dec 4;80(4):396-8. Am J Med Genet. 1998. PMID: 9856570

3

Microdissection-based high-resolution genomic array analysis of two patients with cytogenetically identical interstitial deletions of chromosome 1q but distinct clinical phenotypes.

Rice GM, Qi Z, Selzer R, Richmond T, Thompson K, Pauli RM, Yu J. Rice GM, et al. Among authors: thompson k. Am J Med Genet A. 2006 Aug 1;140(15):1637-43. doi: 10.1002/ajmg.a.31349. Am J Med Genet A. 2006. PMID: 16835927

4

Monosomy 18q12.1----21.1: a recognizable aneuploidy syndrome? Report of a patient and review of the literature.

Krasikov N, Thompson K, Sekhon GS. Krasikov N, et al. Among authors: thompson k. Am J Med Genet. 1992 Jun 1;43(3):531-4. doi: 10.1002/ajmg.1320430306. Am J Med Genet. 1992. PMID: 1376552 Review.

5

Absence of predictable phenotypic expression in proximal 15q duplications.

Ludowese CJ, Thompson KJ, Sekhon GS, Pauli RM. Ludowese CJ, et al. Among authors: thompson kj. Clin Genet. 1991 Sep;40(3):194-201. doi: 10.1111/j.1399-0004.1991.tb03076.x. Clin Genet. 1991. PMID: 1773534

6

Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype.

Smith TB, Kopajtich R, Demain LAM, Rea A, Thomas HB, Schiff M, Beetz C, Joss S, Conway GS, Shukla A, Yeole M, Radhakrishnan P, Azzouz H, Ben Chehida A, Elmaleh-Bergès M, Glasgow RIC, Thompson K, Oláhová M, He L, Jenkinson EM, Jahic A, Belyantseva IA, Barzik M, Urquhart JE, O'Sullivan J, Williams SG, Bhaskar SS, Carrera S, Blakes AJM, Banka S, Yue WW, Ellingford JM, Houlden H; DDD Study; Munro KJ, Friedman TB, Taylor RW, Prokisch H, O'Keefe RT, Newman WG. Smith TB, et al. Among authors: thompson k. Am J Hum Genet. 2025 Jan 2;112(1):59-74. doi: 10.1016/j.ajhg.2024.11.007. Epub 2024 Dec 18. Am J Hum Genet. 2025. PMID: 39701103 Free article.

7

#ExploratoryAnalysisOfSentimentTowardABAonTwitter.

Malkin A, Riosa PB, Mullins L, Thompson K, Kretschmer A. Malkin A, et al. Among authors: thompson k. Behav Anal Pract. 2024 Apr 1;17(4):1104-1112. doi: 10.1007/s40617-024-00929-x. eCollection 2024 Dec. Behav Anal Pract. 2024. PMID: 39790931

8

Biomarkers.

Jannati A, Thompson K, Toro-Serey C, Higgins C, Banks R, Showalter J, Bates D, Tobyne S, Pascual-Leone A. Jannati A, et al. Among authors: thompson k. Alzheimers Dement. 2024 Dec;20 Suppl 2:e093435. doi: 10.1002/alz.093435. Alzheimers Dement. 2024. PMID: 39785338

9

Biomarkers.

Banks R, Thompson K, Jannati A, Tobyne S, Showalter J, Bates D, Pascual-Leone A. Banks R, et al. Among authors: thompson k. Alzheimers Dement. 2024 Dec;20 Suppl 2:e089936. doi: 10.1002/alz.089936. Alzheimers Dement. 2024. PMID: 39784178

10

AI in Hepatology: Revolutionizing the Diagnosis and Management of Liver Disease.

Malik S, Das R, Thongtan T, Thompson K, Dbouk N. Malik S, et al. Among authors: thompson k. J Clin Med. 2024 Dec 22;13(24):7833. doi: 10.3390/jcm13247833. J Clin Med. 2024. PMID: 39768756 Free PMC article. Review.

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