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Items: 23

1.

Women's experiences of diagnosis and management of polycystic ovary syndrome: a mixed-methods study in general practice.

Hillman SC, Bryce C, Caleyachetty R, Dale J.

Br J Gen Pract. 2020 Mar 9. pii: bjgp20X708881. doi: 10.3399/bjgp20X708881. [Epub ahead of print]

PMID:
32152043
2.

Polycystic ovarian syndrome: an under-recognised problem?

Hillman SC, Dale J.

Br J Gen Pract. 2018 May;68(670):244. doi: 10.3399/bjgp18X696101. No abstract available.

3.

Genomics in general practice: Generation Genome.

Hillman SC, Dale J.

Br J Gen Pract. 2017 Dec;67(665):540-541. doi: 10.3399/bjgp17X693533. No abstract available.

4.

Parental experiences of prenatal whole exome sequencing (WES) in cases of ultrasound diagnosed fetal structural anomaly.

Quinlan-Jones E, Hillman SC, Kilby MD, Greenfield SM.

Prenat Diagn. 2017 Dec;37(12):1225-1231. doi: 10.1002/pd.5172. Epub 2017 Nov 10.

PMID:
29049852
5.

Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.

Quinlan-Jones E, Kilby MD, Greenfield S, Parker M, McMullan D, Hurles ME, Hillman SC.

Prenat Diagn. 2016 Oct;36(10):935-941. doi: 10.1002/pd.4916. Epub 2016 Sep 18.

PMID:
27550507
6.

Intrahepatic cholestasis of pregnancy.

Hillman SC, Stokes-Lampard H, Kilby MD.

BMJ. 2016 Apr 21;353:i1236. doi: 10.1136/bmj.i1236. No abstract available.

PMID:
27103313
7.

Comparison of Solomon technique with selective laser ablation for twin-twin transfusion syndrome: a systematic review.

Dhillon RK, Hillman SC, Pounds R, Morris RK, Kilby MD.

Ultrasound Obstet Gynecol. 2015 Nov;46(5):526-33. doi: 10.1002/uog.14813. Review.

8.

Prenatal exome sequencing for fetuses with structural abnormalities: the next step.

Hillman SC, Willams D, Carss KJ, McMullan DJ, Hurles ME, Kilby MD.

Ultrasound Obstet Gynecol. 2015 Jan;45(1):4-9. doi: 10.1002/uog.14653. Epub 2014 Dec 9. No abstract available.

9.

BAC chromosomal microarray for prenatal detection of chromosome anomalies in fetal ultrasound anomalies: an economic evaluation.

Hillman SC, Barton PM, Roberts TE, Maher ER, McMullan DM, Kilby MD.

Fetal Diagn Ther. 2014;36(1):49-58. doi: 10.1159/000358387. Epub 2014 Jun 13.

PMID:
24943865
10.

Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound.

Carss KJ, Hillman SC, Parthiban V, McMullan DJ, Maher ER, Kilby MD, Hurles ME.

Hum Mol Genet. 2014 Jun 15;23(12):3269-77. doi: 10.1093/hmg/ddu038. Epub 2014 Jan 29.

11.

Placenta chorioangioma: a rare case and systematic review of literature.

Al Wattar BH, Hillman SC, Marton T, Foster K, Kilby MD.

J Matern Fetal Neonatal Med. 2014 Jul;27(10):1055-63. doi: 10.3109/14767058.2013.847424. Epub 2013 Oct 17. Review.

PMID:
24460422
12.

Exome Sequencing in Fetuses with Structural Malformations.

Mackie FL, Carss KJ, Hillman SC, Hurles ME, Kilby MD.

J Clin Med. 2014 Jul 8;3(3):747-62. doi: 10.3390/jcm3030747. Review.

13.

Single-twin demise: pregnancy outcome.

Shek NW, Hillman SC, Kilby MD.

Best Pract Res Clin Obstet Gynaecol. 2014 Feb;28(2):249-63. doi: 10.1016/j.bpobgyn.2013.11.003. Epub 2013 Dec 3. Review.

PMID:
24361180
14.

Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data: does increased diagnostic power outweigh the dilemma of rare variants.

Hillman SC, McMullan DJ, Maher ER, Kilby MD.

BJOG. 2013 Sep;120(10):1296. doi: 10.1111/1471-0528.12378. No abstract available.

15.

How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?

Hillman SC, McMullan DJ, Silcock L, Maher ER, Kilby MD.

J Matern Fetal Neonatal Med. 2014 May;27(7):649-57. doi: 10.3109/14767058.2013.825601. Epub 2013 Aug 19.

PMID:
23869996
16.

Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta-analysis.

Dhillon RK, Hillman SC, Morris RK, McMullan D, Williams D, Coomarasamy A, Kilby MD.

BJOG. 2014 Jan;121(1):11-21. doi: 10.1111/1471-0528.12382. Epub 2013 Jul 17. Review.

17.

"If it helps..." the use of microarray technology in prenatal testing: patient and partners reflections.

Hillman SC, Skelton J, Quinlan-Jones E, Wilson A, Kilby MD.

Am J Med Genet A. 2013 Jul;161A(7):1619-27. doi: 10.1002/ajmg.a.35981. Epub 2013 May 21.

PMID:
23696517
18.

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.

Hillman SC, McMullan DJ, Hall G, Togneri FS, James N, Maher EJ, Meller CH, Williams D, Wapner RJ, Maher ER, Kilby MD.

Ultrasound Obstet Gynecol. 2013 Jun;41(6):610-20. doi: 10.1002/uog.12464. Epub 2013 May 7. Review.

19.

Microarray comparative genomic hybridization in prenatal diagnosis: a review.

Hillman SC, McMullan DJ, Williams D, Maher ER, Kilby MD.

Ultrasound Obstet Gynecol. 2012 Oct;40(4):385-91. doi: 10.1002/uog.11180. Epub 2012 Sep 17. Review.

20.

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.

Hillman SC, McMullan DJ, Maher ER, Kilby MD.

BJOG. 2012 Sep;119(10):1281-2; author reply 1282. doi: 10.1111/j.1471-0528.2012.03418.x. No abstract available.

21.

Co-twin prognosis after single fetal death: a systematic review and meta-analysis.

Hillman SC, Morris RK, Kilby MD.

Obstet Gynecol. 2011 Oct;118(4):928-40. doi: 10.1097/AOG.0b013e31822f129d. Review.

PMID:
21934458
22.

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.

Hillman SC, Pretlove S, Coomarasamy A, McMullan DJ, Davison EV, Maher ER, Kilby MD.

Ultrasound Obstet Gynecol. 2011 Jan;37(1):6-14. doi: 10.1002/uog.7754. Review.

23.

Single twin demise: consequence for survivors.

Hillman SC, Morris RK, Kilby MD.

Semin Fetal Neonatal Med. 2010 Dec;15(6):319-26. doi: 10.1016/j.siny.2010.05.004. Epub 2010 Jul 2. Review.

PMID:
20584634

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