Elsner T - Search Results

1

Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function.

Malhotra A, Peiffer AP, Ryujin DT, Elsner T, Kanner RE, Leppert MF, Hasstedt SJ. Malhotra A, et al. Among authors: elsner t. Am J Respir Crit Care Med. 2003 Sep 1;168(5):556-61. doi: 10.1164/rccm.200303-410OC. Epub 2003 Jun 5. Am J Respir Crit Care Med. 2003. PMID: 12791583

2

A primary genetic linkage map for human chromosome 12.

O'Connell P, Lathrop GM, Law M, Leppert M, Nakamura Y, Hoff M, Kumlin E, Thomas W, Elsner T, Ballard L, et al. O'Connell P, et al. Among authors: elsner t. Genomics. 1987 Sep;1(1):93-102. doi: 10.1016/0888-7543(87)90110-8. Genomics. 1987. PMID: 3478299

3

A genetic linkage map with 29 loci spanning human chromosome 13q.

Gerken S, Leppert M, O'Connell P, Cavenee W, James CD, Ballard L, Stauffer D, Elsner T, Plaetke R, Lalouel JM, et al. Gerken S, et al. Among authors: elsner t. Genomics. 1993 May;16(2):515-9. doi: 10.1006/geno.1993.1219. Genomics. 1993. PMID: 8100218

4

Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p.

Drayna D, Coon H, Kim UK, Elsner T, Cromer K, Otterud B, Baird L, Peiffer AP, Leppert M; Utah Genetic Reference Project. Drayna D, et al. Among authors: elsner t. Hum Genet. 2003 May;112(5-6):567-72. doi: 10.1007/s00439-003-0911-y. Epub 2003 Mar 6. Hum Genet. 2003. PMID: 12624758

5

A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels.

Gerken SC, Albertsen H, Elsner T, Ballard L, Holik P, Lawrence E, Moore M, Zhao X, White R. Gerken SC, et al. Among authors: elsner t. Am J Hum Genet. 1995 Feb;56(2):484-99. Am J Hum Genet. 1995. PMID: 7847385 Free PMC article.

6

Polymorphic SSR (simple-sequence-repeat) markers for chromosome 20.

Melis R, Bradley P, Elsner T, Robertson M, Lawrence E, Gerken S, Albertsen H, White R. Melis R, et al. Among authors: elsner t. Genomics. 1993 Apr;16(1):56-62. doi: 10.1006/geno.1993.1140. Genomics. 1993. PMID: 8486385

7

Breakpoint analysis: precise localization of genetic markers by means of nonstatistical computation using relatively few genotypes.

Elsner TI, Albertsen H, Gerken SC, Cartwright P, White R. Elsner TI, et al. Am J Hum Genet. 1995 Feb;56(2):500-7. Am J Hum Genet. 1995. PMID: 7847386 Free PMC article.

8

The CEPH consortium linkage map of human chromosome 1.

Dracopoli NC, O'Connell P, Elsner TI, Lalouel JM, White RL, Buetow KH, Nishimura DY, Murray JC, Helms C, Mishra SK, et al. Dracopoli NC, et al. Among authors: elsner ti. Genomics. 1991 Apr;9(4):686-700. doi: 10.1016/0888-7543(91)90362-i. Genomics. 1991. PMID: 2037294

9

A Cluster Randomised Control Trial of an SMS-Based Intervention to Promote Antenatal Health amongst Pregnant Women in a Remote, Highland Region of Vietnam.

Dao BTT, Trinh HT, Lai PH, Elsner T, Kane S, Nguyen L. Dao BTT, et al. Among authors: elsner t. Healthcare (Basel). 2023 Aug 28;11(17):2407. doi: 10.3390/healthcare11172407. Healthcare (Basel). 2023. PMID: 37685444 Free PMC article.

10

Databases for Congenital Heart Defect Public Health Studies Across the Lifespan.

Riehle-Colarusso TJ, Bergersen L, Broberg CS, Cassell CH, Gray DT, Grosse SD, Jacobs JP, Jacobs ML, Kirby RS, Kochilas L, Krishnaswamy A, Marelli A, Pasquali SK, Wood T, Oster ME; Congenital Heart Public Health Consortium. Riehle-Colarusso TJ, et al. J Am Heart Assoc. 2016 Oct 26;5(11):e004148. doi: 10.1161/JAHA.116.004148. J Am Heart Assoc. 2016. PMID: 27912209 Free PMC article. Review. No abstract available.

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