Cochrane S - Search Results

1

An evaluation of common breast cancer gene mutations in a population of Ashkenazi Jews.

Lalloo F, Cochrane S, Bulman B, Varley J, Elles R, Howell A, Evans DG. Lalloo F, et al. Among authors: cochrane s. J Med Genet. 1998 Jan;35(1):10-2. doi: 10.1136/jmg.35.1.10. J Med Genet. 1998. PMID: 9475087 Free PMC article.

2

A previously undescribed mutation within the tetramerisation domain of TP53 in a family with Li-Fraumeni syndrome.

Varley JM, McGown G, Thorncroft M, Cochrane S, Morrison P, Woll P, Kelsey AM, Mitchell EL, Boyle J, Birch JM, Evans DG. Varley JM, et al. Among authors: cochrane s. Oncogene. 1996 Jun 6;12(11):2437-42. Oncogene. 1996. PMID: 8649785

3

X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.

Cochrane S, Bergoffen J, Fairweather ND, Müller E, Mostacciuolo ML, Monaco AP, Fischbeck KH, Haites NE. Cochrane S, et al. J Med Genet. 1994 Mar;31(3):193-6. doi: 10.1136/jmg.31.3.193. J Med Genet. 1994. PMID: 7912286 Free PMC article.

4

Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1).

Fairweather N, Bell C, Cochrane S, Chelly J, Wang S, Mostacciuolo ML, Monaco AP, Haites NE. Fairweather N, et al. Among authors: cochrane s. Hum Mol Genet. 1994 Jan;3(1):29-34. doi: 10.1093/hmg/3.1.29. Hum Mol Genet. 1994. PMID: 8162049

5

Consortium fine localization of X-linked Charcot-Marie-Tooth disease (CMTX1): additional support that connexin32 is the defect in CMTX1.

Pericak-Vance MA, Barker DF, Bergoffen JA, Chance P, Cochrane S, Dahl N, Exler MC, Fain PR, Fairweather ND, Fischbeck K, et al. Pericak-Vance MA, et al. Among authors: cochrane s. Hum Hered. 1995 May-Jun;45(3):121-8. doi: 10.1159/000154272. Hum Hered. 1995. PMID: 7615296

6

Gene structure and promoter functional analysis of the marmoset type II GnRH receptor.

Faurholm B, Cochrane S, Millar RR, Katz AA. Faurholm B, et al. Among authors: cochrane s. J Mol Endocrinol. 2007 Aug;39(2):91-104. doi: 10.1677/JME-06-0064. J Mol Endocrinol. 2007. PMID: 17693609

7

Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family. Mutations in brief no. 158. Online.

Booth DR, Gillmore JD, Persey MR, Booth SE, Cafferty KD, Tennent GA, Madhoo S, Cochrane SW, Whitehead TC, Pasvol G, Hawkins PN. Booth DR, et al. Among authors: cochrane sw. Hum Mutat. 1998;12(2):135. doi: 10.1002/(SICI)1098-1004(1998)12:2<135::AID-HUMU10>3.0.CO;2-6. Hum Mutat. 1998. PMID: 10694917

8

Home and outpatient versus in-hospital initiation of non-invasive ventilation in people with neuromuscular and restrictive thoracic disorders: a network meta-analysis.

Léotard A, Khouri C, Saulnier L, Delorme M, Prigent H, Borel JC, Lebret M. Léotard A, et al. Thorax. 2025 Jun 30:thorax-2024-222634. doi: 10.1136/thorax-2024-222634. Online ahead of print. Thorax. 2025. PMID: 40588414

We used MEDLINE, Web of Science and the CENTRAL (Cochrane Central Register of Controlled Trials) to identify randomised controlled trials (RCTs), controlled and uncontrolled prospective studies comparing NIV efficacy between home and outpatient, and in-hospital initiation. …

We used MEDLINE, Web of Science and the CENTRAL (Cochrane Central Register of Controlled Trials) to identify randomised controlled tr …

9

The Effectiveness of Melatonin for Sleep Disturbances in Parkinson' Disease: Systematic Review and Meta-Analysis.

Yousef O, Abouelmagd ME, Khaddam H, Shbani A, Yousef R, Meshref M, Hanafi I. Yousef O, et al. J Sleep Res. 2025 Jun 30:e70097. doi: 10.1111/jsr.70097. Online ahead of print. J Sleep Res. 2025. PMID: 40588412 Review.

However, its efficacy in PD remains unclear due to inconclusive findings across studies, warranting a systematic review to synthesise the available evidence. We searched PubMed, Cochrane, Web of Science, and Scopus for RCTs up to May 2025. Study quality was evaluated using …

However, its efficacy in PD remains unclear due to inconclusive findings across studies, warranting a systematic review to synthesise the av …

10

[Multi-omics Mendelian randomization study on the causality between non-ionizing radiation and facial aging].

He ZC, Shang YX, Xu XP, Jia CY, Wang YP. He ZC, et al. Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2025 Jun 20;41(6):594-603. doi: 10.3760/cma.j.cn501225-20240830-00320. Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2025. PMID: 40588408 Chinese.

For the selected non-ionizing radiation-associated SNPs, heterogeneity was tested by Cochran Q test, horizontal pleiotropy was assessed by the MR-Egger intercept test and MR-PRESSO test, and robustness was evaluated via leave-one-out analysis. ...For these 20 non-ionizing …

For the selected non-ionizing radiation-associated SNPs, heterogeneity was tested by Cochran Q test, horizontal pleiotropy was assess …

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