Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Hongyan Chai"'
Autor:
Autumn DiAdamo, Hongyan Chai, Mei Ling Chong, Guilin Wang, Jiadi Wen, Yong-Hui Jiang, Peining Li
Publikováno v:
Global Medical Genetics, Vol 11, Iss 01, Pp 123-131 (2024)
Background A retrospective study was performed to evaluate the patterns of cytogenomic findings detected from a case series of products of conception (POC) in recurrent pregnancy loss (RPL) over a 16-year period from 2007 to 2023.
Externí odkaz:
https://doaj.org/article/b5a57dd33fbc45bcafbbfdc3162cd114
Autor:
Gang Peng, Qinghua Zhou, Hongyan Chai, Jiadi Wen, Hongyu Zhao, Hugh S. Taylor, Yong‐Hui Jiang, Peining Li
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 8, Pp n/a-n/a (2023)
Abstract A meta‐analysis on seven large case series (>1000 cases) of chromosome microarray analysis (CMA) on products of conceptions (POC) evaluated the diagnostic yields of genomic disorders and syndromic pathogenic copy number variants (pCNVs) fr
Externí odkaz:
https://doaj.org/article/b6114eb278a54495b6af068716582854
Autor:
Xiaolei Xie, Hongyan Chai, Autumn DiAdamo, Brittany Grommisch, Jiadi Wen, Hui Zhang, Peining Li
Publikováno v:
Global Medical Genetics, Vol 09, Iss 02, Pp 166-174 (2022)
Background Cytogenomic analyses have been used to detect pathogenic copy number variants. Patients with deletions at 6q26-q27 present variable clinical features. We reported clinical and cytogenomic findings of eight unrelated patients with a deletio
Externí odkaz:
https://doaj.org/article/a942fe18a63f46078e062d3eaae1782c
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100697- (2023)
Externí odkaz:
https://doaj.org/article/dc32c9c017a14512bc28091566f66ab6
Autor:
Gang Peng, Hongyan Chai, Weizhen Ji, Yufei Lu, Shengming Wu, Hongyu Zhao, Peining Li, Qiping Hu
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-9 (2021)
Abstract Background Oligonucleotide array comparative genomic hybridization (aCGH) analysis has been used for detecting somatic copy number alterations (CNAs) in various types of tumors. This study aimed to assess the clinical utility of aCGH for cas
Externí odkaz:
https://doaj.org/article/a92696e840d642dbac06369a4ed04501
Autor:
Jiadi Wen, Brittany Grommisch, Autumn DiAdamo, Hongyan Chai, Sok Meng Evelyn Ng, Pei Hui, Allen Bale, Winifred Mak, Guilin Wang, Peining Li
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Background The OncoScan microarray assay (OMA) using highly multiplexed molecular inversion probes for single nucleotide polymorphism (SNP) loci enabled the detection of cytogenomic abnormalities of chromosomal imbalances and pathogenic copy
Externí odkaz:
https://doaj.org/article/0333816ab88448a3959fb519cc738319
Publikováno v:
Case Reports in Genetics, Vol 2022 (2022)
Chromosome and array comparative genomic hybridization (aCGH) analyses were performed on two cases of well-differentiated liposarcoma (WDLPS) and two cases of dedifferentiated liposarcoma (DDLPS). The results revealed the characteristic giant ring (G
Externí odkaz:
https://doaj.org/article/7b7bc15bb6fb4e9d951ba6661a3d7ca0
Autor:
Jiadi Wen, Kathleen Comerford, Zhiyong Xu, Weiqing Wu, Katherine Amato, Brittany Grommisch, Autumn DiAdamo, Fang Xu, Hongyan Chai, Peining Li
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-10 (2019)
Abstract Background Regions of homozygosity (ROH) are continuous homozygous segments commonly seen in the human genome. The integration of single nucleotide polymorphism (SNP) probes into current array comparative genomic hybridization (aCGH) analysi
Externí odkaz:
https://doaj.org/article/5bbebd77419b4c50a9f64530c0d6f736
Autor:
Xiaolei Xie, Weihe Tan, Fuguang Li, Eric Carrano, Paola Ramirez, Autumn DiAdamo, Brittany Grommisch, Katherine Amato, Hongyan Chai, Jiadi Wen, Peining Li
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background Follow‐up cytogenetic analysis has been recommended for cases with positive noninvasive prenatal screening (NIPS) results. This study of five cases with numerical and structural sex chromosomal abnormalities (SCA) and a review o
Externí odkaz:
https://doaj.org/article/82ae4012a1984e3fad6e8045971b483c
Autor:
Marie Zerjav, Autumn DiAdamo, Brittany Grommisch, Amato Katherine, Hongyan Chai, Gang Peng, Peining Li
Publikováno v:
Case Reports in Genetics, Vol 2020 (2020)
Salivary gland tumors (SGTs) of parotid origin are a group of diverse neoplasms which are difficult to classify due to their rarity and similar morphologic patterns. Chromosome analysis can detect clonal abnormalities, and array comparative genomic h
Externí odkaz:
https://doaj.org/article/19c5e57adc534cbbad3ab5828ccc6f11