Eli Marie Grindedal
Overview
Explore the profile of Eli Marie Grindedal including associated specialties, affiliations and a list of published articles.
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37
Citations
1231
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Recent Articles
1.
Hyldebrandt H, Stormorken A, Vitelli V, Maehle L, Schlichting E, Grindedal E
Eur J Surg Oncol
. 2025 Jan;
51(3):109571.
PMID: 39765192
Background: Risk reducing mastectomy (RRM) is an option for women with pathogenic germline variants in BRCA1 or BRCA2 (BRCA1/2). This study investigates and compares RRM-uptake among Norwegian BRCA1/2 carriers from...
2.
Srinivasan S, Kryza T, Bock N, Tse B, Sokolowski K, Janaththani P, et al.
Nat Commun
. 2024 Nov;
15(1):9587.
PMID: 39505858
Genetic variation at the 19q13.3 KLK locus is linked with prostate cancer susceptibility in men. The non-synonymous KLK3 single nucleotide polymorphism (SNP), rs17632542 (c.536 T > C; Ile163Thr-substitution in PSA)...
3.
Sjursen W, Hyldebrandt H, Lavik L, Haukanes B, Ariansen S, Briskemyr S, et al.
Hered Cancer Clin Pract
. 2024 Sep;
22(1):20.
PMID: 39334433
Background: In Norway, we have offered testing of PMS2 since 2006, and have a large national cohort of carriers. The aim of this study was to describe all PMS2 variants...
4.
Hyldebrandt H, Grindedal E, Huppertz-Hauss G, Vitelli V, Johansen N, Stormorken A
Scand J Gastroenterol
. 2024 Jul;
59(8):1015-1020.
PMID: 38946231
Background And Aims: Women with Lynch Syndrome (LS) have a high risk of colorectal and endometrial cancer. They are recommended regular colonoscopies, and some choose prophylactic hysterectomy. The aim of...
5.
Grindedal E, Zucknick M, Stormorken A, Ronne E, Tandstad N, Isaacs W, et al.
Prostate
. 2024 Apr;
84(10):945-953.
PMID: 38629217
Background: Pathogenic germline variants in the mismatch repair (MMR) genes are associated with an increased risk of prostate cancer (PCa). Since 2010 we have recommended MMR carriers annual PSA testing...
6.
Bjornstad P, Aalokken R, Asheim J, Sundaram A, Felde C, Ostby G, et al.
Eur J Hum Genet
. 2024 Jan;
32(5):601-602.
PMID: 38172175
No abstract available.
7.
Bjornstad P, Aalokken R, Asheim J, Sundaram A, Felde C, Ostby G, et al.
Eur J Hum Genet
. 2023 Nov;
32(5):513-520.
PMID: 38030917
Lynch Syndrome (LS) is a hereditary cancer syndrome caused by pathogenic germline variants in one of the four mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2. It is characterized...
8.
Wang A, Shen J, Rodriguez A, Saunders E, Chen F, Janivara R, et al.
Nat Genet
. 2023 Nov;
55(12):2065-2074.
PMID: 37945903
The transferability and clinical value of genetic risk scores (GRSs) across populations remain limited due to an imbalance in genetic studies across ancestrally diverse populations. Here we conducted a multi-ancestry...
9.
Darst B, Shen J, Madduri R, Rodriguez A, Xiao Y, Sheng X, et al.
Am J Hum Genet
. 2023 Jun;
110(7):1200-1206.
PMID: 37311464
Genome-wide polygenic risk scores (GW-PRSs) have been reported to have better predictive ability than PRSs based on genome-wide significance thresholds across numerous traits. We compared the predictive ability of several...
10.
Darst B, Shen J, Madduri R, Rodriguez A, Xiao Y, Sheng X, et al.
medRxiv
. 2023 Jun;
PMID: 37292833
Genome-wide polygenic risk scores (GW-PRS) have been reported to have better predictive ability than PRS based on genome-wide significance thresholds across numerous traits. We compared the predictive ability of several...