Muhammad N - Search Results

1

Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan.

Rashid MU, Muhammad N, Faisal S, Amin A, Hamann U. Rashid MU, et al. Among authors: muhammad n. BMC Cancer. 2013 Jun 27;13:312. doi: 10.1186/1471-2407-13-312. BMC Cancer. 2013. PMID: 23806170 Free PMC article.

2

Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients.

Rashid MU, Gull S, Asghar K, Muhammad N, Amin A, Hamann U. Rashid MU, et al. Among authors: muhammad n. Fam Cancer. 2012 Jun;11(2):307-11. doi: 10.1007/s10689-012-9509-7. Fam Cancer. 2012. PMID: 22311583

3

Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.

Rashid MU, Muhammad N, Faisal S, Amin A, Hamann U. Rashid MU, et al. Among authors: muhammad n. Breast Cancer Res Treat. 2014 Jun;145(3):775-84. doi: 10.1007/s10549-014-2972-0. Epub 2014 May 7. Breast Cancer Res Treat. 2014. PMID: 24800917

4

BRCA1 genetic testing in a Pakistani breast-ovarian cancer family with multiple consanguineous marriages.

Rashid MU, Muhammad N, Iqbal K, Yusuf HA, Hamann U. Rashid MU, et al. Among authors: muhammad n. Clin Genet. 2015 Aug;88(2):198-9. doi: 10.1111/cge.12533. Epub 2014 Nov 28. Clin Genet. 2015. PMID: 25430881 No abstract available.

5

Absence of the FANCM c.5101C>T mutation in BRCA1/2-negative triple-negative breast cancer patients from Pakistan.

Rashid MU, Muhammad N, Khan FA, Hamann U. Rashid MU, et al. Among authors: muhammad n. Breast Cancer Res Treat. 2015 Jul;152(1):229-230. doi: 10.1007/s10549-015-3457-5. Epub 2015 Jun 12. Breast Cancer Res Treat. 2015. PMID: 26067930 No abstract available.

6

Association between the BsmI Polymorphism in the Vitamin D Receptor Gene and Breast Cancer Risk: Results from a Pakistani Case-Control Study.

Rashid MU, Muzaffar M, Khan FA, Kabisch M, Muhammad N, Faiz S, Loya A, Hamann U. Rashid MU, et al. Among authors: muhammad n. PLoS One. 2015 Oct 30;10(10):e0141562. doi: 10.1371/journal.pone.0141562. eCollection 2015. PLoS One. 2015. PMID: 26517870 Free PMC article.

7

A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome.

Rashid MU, Naeemi H, Muhammad N, Loya A, Yusuf MA, Lubiński J, Jakubowska A, Hamann U. Rashid MU, et al. Among authors: muhammad n. Hered Cancer Clin Pract. 2016 Jul 12;14:14. doi: 10.1186/s13053-016-0056-3. eCollection 2016. Hered Cancer Clin Pract. 2016. PMID: 27413415 Free PMC article.

8

High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients.

Rashid MU, Muhammad N, Bajwa S, Faisal S, Tahseen M, Bermejo JL, Amin A, Loya A, Hamann U. Rashid MU, et al. Among authors: muhammad n. BMC Cancer. 2016 Aug 23;16(1):673. doi: 10.1186/s12885-016-2698-y. BMC Cancer. 2016. PMID: 27553291 Free PMC article.

9

Contribution of BRCA1 large genomic rearrangements to early-onset and familial breast/ovarian cancer in Pakistan.

Rashid MU, Muhammad N, Amin A, Loya A, Hamann U. Rashid MU, et al. Among authors: muhammad n. Breast Cancer Res Treat. 2017 Jan;161(2):191-201. doi: 10.1007/s10549-016-4044-0. Epub 2016 Nov 8. Breast Cancer Res Treat. 2017. PMID: 27826754

10

Prevalence of PALB2 Germline Mutations in Early-onset and Familial Breast/Ovarian Cancer Patients from Pakistan.

Rashid MU, Khan FA, Muhammad N, Loya A, Hamann U. Rashid MU, et al. Among authors: muhammad n. Cancer Res Treat. 2019 Jul;51(3):992-1000. doi: 10.4143/crt.2018.356. Epub 2018 Oct 11. Cancer Res Treat. 2019. PMID: 30309218 Free PMC article.

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