Rothenmund H[Author] - Search Results

Year	Number of Results
1997	1
2000	1
2002	1
2004	1
2007	3
2008	1
2009	1
2010	1
2011	4
2012	2
2013	1
2014	2
2015	3
2019	2
2020	1
2021	1
2022	1
2023	2
2024	1

1

Psychosocial Impact of Lynch Syndrome on Affected Individuals and Families.

Galiatsatos P, Rothenmund H, Aubin S, Foulkes WD. Galiatsatos P, et al. Among authors: rothenmund h. Dig Dis Sci. 2015 Aug;60(8):2246-50. doi: 10.1007/s10620-015-3626-8. Epub 2015 Mar 19. Dig Dis Sci. 2015. PMID: 25786861 Review.

2

A Canadian Provincial Screening Program for Lynch Syndrome.

Stone JK, Winter R, Khan D, Rothenmund H, Klein J, Chodirker B, Wightman R, Kim CA, Nugent Z, Singh H. Stone JK, et al. Among authors: rothenmund h. Am J Gastroenterol. 2023 Feb 1;118(2):345-353. doi: 10.14309/ajg.0000000000002059. Epub 2022 Oct 11. Am J Gastroenterol. 2023. PMID: 36219179

3

Province-Wide Ascertainment of Lynch Syndrome in Manitoba.

Rothenmund H, Lambert P, Khan D, Kim C, Sharma B, Serfas K, Chodirker B, Singh H. Rothenmund H, et al. Clin Gastroenterol Hepatol. 2024 Mar;22(3):642-652.e2. doi: 10.1016/j.cgh.2023.10.005. Epub 2023 Oct 23. Clin Gastroenterol Hepatol. 2024. PMID: 37879520

4

Hereditary colorectal cancer screening: A 10-year longitudinal cohort study following an educational intervention.

Carroll JC, Permaul JA, Semotiuk K, Yung EM, Blaine S, Dicks E, Warner E, Rothenmund H, Esplen MJ, Moineddin R, McLaughlin J. Carroll JC, et al. Among authors: rothenmund h. Prev Med Rep. 2020 Sep 23;20:101189. doi: 10.1016/j.pmedr.2020.101189. eCollection 2020 Dec. Prev Med Rep. 2020. PMID: 33117641 Free PMC article.

5

Familial transmission of a small supernumerary marker chromosome 8 identified by FISH: an update.

Rothenmund H, Chudley AE, Dawson AJ. Rothenmund H, et al. Am J Med Genet. 1997 Oct 31;72(3):339-42. doi: 10.1002/(sici)1096-8628(19971031)72:3<339::aid-ajmg17>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9332666 Review.

6

Suboptimal Adherence in Clinical Practice to Guidelines Recommendation to Screen for Lynch Syndrome.

Jain A, Shafer L, Rothenmund H, Kim CA, Samadder J, Gupta S, Singh H. Jain A, et al. Among authors: rothenmund h. Dig Dis Sci. 2019 Dec;64(12):3489-3501. doi: 10.1007/s10620-019-05692-6. Epub 2019 Jun 11. Dig Dis Sci. 2019. PMID: 31187321

7

Telephone versus in-person colorectal cancer risk and screening intervention for first-degree relatives: A randomized controlled trial.

Esplen MJ, Harrington S, Leung YW, Aronson M, Rothenmund H, Semotiuk K, Wong J, Gallinger S, Dicks E, McLaughlin J. Esplen MJ, et al. Among authors: rothenmund h. Cancer. 2019 Jul 1;125(13):2272-2282. doi: 10.1002/cncr.32032. Epub 2019 Mar 12. Cancer. 2019. PMID: 30861097 Free PMC article. Clinical Trial.

8

Germline BRCA1 mutations predispose to pancreatic adenocarcinoma.

Al-Sukhni W, Rothenmund H, Borgida AE, Zogopoulos G, O'Shea AM, Pollett A, Gallinger S. Al-Sukhni W, et al. Among authors: rothenmund h. Hum Genet. 2008 Oct;124(3):271-8. doi: 10.1007/s00439-008-0554-0. Epub 2008 Sep 2. Hum Genet. 2008. PMID: 18762988

9

Immune Checkpoint Inhibition as Primary Adjuvant Therapy for an IDH1-Mutant Anaplastic Astrocytoma in a Patient with CMMRD: A Case Report-Usage of Immune Checkpoint Inhibition in CMMRD.

Rittberg R, Harlos C, Rothenmund H, Das A, Tabori U, Sinha N, Singh H, Chodirker B, Kim CA. Rittberg R, et al. Among authors: rothenmund h. Curr Oncol. 2021 Feb 1;28(1):757-766. doi: 10.3390/curroncol28010074. Curr Oncol. 2021. PMID: 33535600 Free PMC article.

10

The prevalence of BRCA2 mutations in familial pancreatic cancer.

Couch FJ, Johnson MR, Rabe KG, Brune K, de Andrade M, Goggins M, Rothenmund H, Gallinger S, Klein A, Petersen GM, Hruban RH. Couch FJ, et al. Among authors: rothenmund h. Cancer Epidemiol Biomarkers Prev. 2007 Feb;16(2):342-6. doi: 10.1158/1055-9965.EPI-06-0783. Cancer Epidemiol Biomarkers Prev. 2007. PMID: 17301269

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