Search Results - "Vestergaard EM"

In vitro compatibility screening of Bacillus pumilus and Bacillus altitudinis strains with selected candidate prebiotics for in ovo application of synergistic synbiotics.

Authors: Akhavan, Niloofar Hrynkiewicz, Katarzyna Thiem, Dominika et al.

Source: Applied Microbiology & Biotechnology; 12/9/2025, Vol. 109 Issue 1, p1-14, 14p

Serum CA 19 − 9 and CA 72 − 4 levels in hashimoto's thyroiditis: a prospective case-control study.

Authors: Demirci, Huseyin Ucgul, Enes Aydogan, Ebru et al.

Source: BMC Endocrine Disorders. 10/1/2025, Vol. 25 Issue 1, p1-7. 7p.

Prenatal diagnosis and pregnancy outcomes of mosaicism detected by CMA-seq.

Authors: Chang, Jiazhen Li, Mengmeng Jiang, Yulin et al.

Source: BMC Pregnancy & Childbirth. 9/1/2025, Vol. 25 Issue 1, p1-11. 11p.

Clinical experience of genome-wide non-invasive prenatal testing as a first-tier screening test in a cohort of 59,771 pregnancies.

Authors: Zhen, Jianxin Zhang, Liting Wang, Huilin et al.

Source: PLoS ONE. 8/18/2025, Vol. 20 Issue 8, p1-14. 14p.

Detection of differentially methylated CpGs between tumour and adjacent benign cells in diagnostic prostate cancer samples.

Authors: FitzGerald, Liesel M. Jung, Chol-hee Wong, Ee Ming et al.

Source: Scientific Reports. 8/2/2024, Vol. 14 Issue 1, p1-8. 8p.

Placental mosaicism in prenatal diagnosis.

Authors: Döttelmayer MSc., Patricia Fauth, Christine

Source: Medizinische Genetik. Apr2026, Vol. 38 Issue 2, p139-149. 11p.

Clinical application of fetal Nuchal Translucency combined with noninvasive prenatal testing in screening chromosome abnormalities.

Authors: Fu, Guangzhen Hu, Shuang

Source: PLoS ONE. 3/16/2026, Vol. 21 Issue 3, p1-9. 9p.

Integrating multi-cohort machine learning and clinical sample validation to explore peripheral blood mRNA diagnostic biomarkers for prostate cancer.

Authors: Zhong, Xingyu Yang, Yuxuan He, Haodong et al.

Source: Cancer Cell International. 4/22/2025, Vol. 25 Issue 1, p1-11. 11p.

ViLR: a novel virtual long read method for breakpoint identification and direct SNP haplotyping in de novo PGT-SR carriers without a proband.

Authors: Xue, Jiangyang Xie, Min Cai, Jie et al.

Source: Reproductive Biology & Endocrinology. 3/5/2025, Vol. 23 Issue 1, p1-14. 14p.

Noninvasive prenatal testing for the detection of fetal chromosome 17 microduplication: clinical implications and findings.

Authors: Shi, Ye Zheng, Fang-xiu Wang, Jing et al.

Source: Molecular Cytogenetics (17558166). 4/22/2024, Vol. 17 Issue 1, p1-5. 5p.

Mosaicism in genetic tumour syndromes.

Authors: Boros M.Sc., Matej Bourdeaut, Franck Fleischmann, Lara S. et al.

Source: Medizinische Genetik. Nov2025, Vol. 37 Issue 4, p279-293. 15p.

The value of increasing sequencing depth for noninvasive prenatal screening for whole chromosomal aneuploidy.

Authors: Wang, Dongmei Guo, Fangfang Hou, Yaping et al.

Source: Scientific Reports. 1/21/2025, Vol. 15 Issue 1, p1-8. 8p.

A simplified MyProstateScore2.0 for high-grade prostate cancer.

Authors: Tang, Tiffany M Zhang, Yuping Kenney, Ana M et al.

Source: Cancer Biomarkers. 2025, Vol. 42 Issue 1, p1-17. 17p.

Immature platelet fraction as a systemic inflammation marker in patients with chronic obstructive pulmonary disease.

Authors: Absieh, Nasser Arslan, Fatma Doğan, Özlem et al.

Source: International Journal of Laboratory Hematology. Oct2024, Vol. 46 Issue 5, p822-829. 8p.

Genetic variation of FUT3 gene in the Han population from Northern China.

Authors: Zhou, Shihang Zheng, Ziwei Wang, Liying et al.

Source: Transfusion Medicine. Oct2024, Vol. 34 Issue 5, p437-444. 8p.

A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case report.

Authors: Li, Yue Wang, Yumeng Ming, Yan et al.

Source: BMC Medical Genomics. 11/1/2021, Vol. 14 Issue 1, p1-7. 7p.

Fetal congenital gastrointestinal obstruction: prenatal diagnosis of chromosome microarray analysis and pregnancy outcomes.

Authors: Ni, Mengyao Zhu, Xiangyu Liu, Wei et al.

Source: BMC Pregnancy & Childbirth. 7/8/2023, Vol. 23 Issue 1, p1-7. 7p.

ASSESSMENT OF CHROMOSOMAL MICROARRAY FINDINGS IN THE MOLECULAR DIAGNOSIS OF CONGENITAL HEART DISEASES.

Alternate Title: KONJENİTAL KALP HASTALIĞININ MOLEKÜLER TANISINDA KROMOZOMAL MİKRODİZİN BULGULARININ DEĞERLENDİRİLMESİ.

Authors: Kayhan, Gülsüm Alpaslan, Ekin Terlemez, Semiha et al.

Source: Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi. 2025, Vol. 88 Issue 4, p321-328. 8p.

A placental trisomy 2 detected by NIPT evolved in a fetal small Supernumerary Marker Chromosome (sSMC).

Authors: Domaradzka, Justyna Deperas, Marta Obersztyn, Ewa et al.

Source: Molecular Cytogenetics (17558166). 3/15/2021, Vol. 14 Issue 1, p1-7. 7p.

Cell‐based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations.

Authors: Hatt, Lotte Singh, Ripudaman Christensen, Rikke et al.

Source: Clinical Case Reports. Dec2020, Vol. 8 Issue 12, p2561-2567. 7p.