OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation
Haowei Du, Angad Jolly, Christopher M. Grochowski, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Haowei Du, Angad Jolly, Christopher M. Grochowski, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 10
Showing 10 citing articles:
Inverted triplications formed by iterative template switches generate structural variant diversity at genomic disorder loci
Christopher M. Grochowski, Jesse D. Bengtsson, Haowei Du, et al.
Cell Genomics (2024) Vol. 4, Iss. 7, pp. 100590-100590
Open Access | Times Cited: 8
Christopher M. Grochowski, Jesse D. Bengtsson, Haowei Du, et al.
Cell Genomics (2024) Vol. 4, Iss. 7, pp. 100590-100590
Open Access | Times Cited: 8
Impact and characterization of serial structural variations across humans and great apes
Wolfram Höps, Tobias Rausch, Michael Jendrusch, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Wolfram Höps, Tobias Rausch, Michael Jendrusch, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders
Tugce Bozkurt‐Yozgatli, Davut Pehli̇van, Richard A. Gibbs, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 2
Tugce Bozkurt‐Yozgatli, Davut Pehli̇van, Richard A. Gibbs, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 2
A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements
Jakob Schuy, Kristine Bilgrav Sæther, Jasmin Lisfeld, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101863-101863
Open Access | Times Cited: 1
Jakob Schuy, Kristine Bilgrav Sæther, Jasmin Lisfeld, et al.
Genetics in Medicine Open (2024) Vol. 2, pp. 101863-101863
Open Access | Times Cited: 1
Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome
Angad Jolly, Haowei Du, Christelle Borel, et al.
Human Genetics and Genomics Advances (2023) Vol. 4, Iss. 3, pp. 100188-100188
Open Access | Times Cited: 2
Angad Jolly, Haowei Du, Christelle Borel, et al.
Human Genetics and Genomics Advances (2023) Vol. 4, Iss. 3, pp. 100188-100188
Open Access | Times Cited: 2
A protospacer adjacent motif‐free, multiplexed, and quantitative nucleic acid detection platform with barcode‐based Cas12a activity
Miaojin Zhou, Chunhua Zhang, Miaomiao Chen, et al.
MedComm (2023) Vol. 4, Iss. 4
Open Access | Times Cited: 2
Miaojin Zhou, Chunhua Zhang, Miaomiao Chen, et al.
MedComm (2023) Vol. 4, Iss. 4
Open Access | Times Cited: 2
VizCNV: An integrated platform for concurrent phased BAF and CNV analysis with trio genome sequencing data
Haowei Du, Ming Yin Lun, Lidiia Gagarina, et al.
(2024)
Open Access
Haowei Du, Ming Yin Lun, Lidiia Gagarina, et al.
(2024)
Open Access
Impact and characterization of serial structural variations across humans and great apes
Wolfram Höps, Tobias Rausch, Peter Ebert, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Wolfram Höps, Tobias Rausch, Peter Ebert, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
SNV/indel hypermutator phenotype in biallelic RAD51C variant - Fanconi anemia
Roni Zemet, Haowei Du, Tomasz Gambin, et al.
Research Square (Research Square) (2023)
Open Access
Roni Zemet, Haowei Du, Tomasz Gambin, et al.
Research Square (Research Square) (2023)
Open Access
SNV/indel hypermutator phenotype in biallelic RAD51C variant: Fanconi anemia
Roni Zemet, Haowei Du, Tomasz Gambin, et al.
Human Genetics (2023) Vol. 142, Iss. 6, pp. 721-733
Open Access
Roni Zemet, Haowei Du, Tomasz Gambin, et al.
Human Genetics (2023) Vol. 142, Iss. 6, pp. 721-733
Open Access
