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Year | Number of Results |
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2019 | 3 |
2022 | 2 |
2023 | 2 |
2024 | 0 |
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Page 1
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Nat Med. 2019 Mar;25(3):439-447. doi: 10.1038/s41591-018-0334-x. Epub 2019 Jan 28.
Nat Med. 2019.
PMID: 30692697
Performance of prenatal cfDNA screening for sex chromosomes.
Martin K, Dar P, MacPherson C, Egbert M, Demko Z, Parmar S, Hashimoto K, Haeri S, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Strong N, Silver RM, Vohra N, Hyett J, Rabinowitz M, Kao C, Hakonarson H, Jacobsson B, Norton ME.
Martin K, et al. Among authors: parmar s.
Genet Med. 2023 Aug;25(8):100879. doi: 10.1016/j.gim.2023.100879. Epub 2023 May 5.
Genet Med. 2023.
PMID: 37154148
Free article.
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Maternal Sex Chromosome Aneuploidy Identified through Noninvasive Prenatal Screening: Clinical Profile and Patient Experience.
Roberts AW, Maisenbacher MK, Parmar S, Wilkinson J, Poll S, Faulkner N, Prakash SK.
Roberts AW, et al. Among authors: parmar s.
Am J Perinatol. 2023 Aug 9. doi: 10.1055/a-2126-7476. Online ahead of print.
Am J Perinatol. 2023.
PMID: 37433314
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Clinician-reported chorionicity and zygosity assignment using single-nucleotide polymorphism-based cell-free DNA: Lessons learned from 55,344 twin pregnancies.
Wojas A, Martin KA, Koyen Malashevich A, Hashimoto K, Parmar S, White R, Demko Z, Billings P, Jelsema R, Rebarber A.
Wojas A, et al. Among authors: parmar s.
Prenat Diagn. 2022 Sep;42(10):1235-1241. doi: 10.1002/pd.6218. Epub 2022 Sep 7.
Prenat Diagn. 2022.
PMID: 35997139
Free PMC article.
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Positive predictive value of a single nucleotide polymorphism (SNP)-based NIPT for aneuploidy in twins: Experience from clinical practice.
Kantor V, Mo L, DiNonno W, Howard K, Palsuledesai CC, Parmar S, Chithiwala Z, Jelsema R, Xu W, Hedriana HL.
Kantor V, et al. Among authors: parmar s.
Prenat Diagn. 2022 Dec;42(13):1587-1593. doi: 10.1002/pd.6262. Epub 2022 Nov 21.
Prenat Diagn. 2022.
PMID: 36336878
Free PMC article.
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Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, Breman A, Xia F, Yang Y, Purgason A, Pourpak A, Chen Z, Wang X, Wang Y, Kulkarni S, Choy KW, Wapner RJ, Van den Veyver IB, Beaudet A, Parmar S, Wong LJ, Eng CM.
Zhang J, et al. Among authors: parmar s.
Nat Med. 2019 Apr;25(4):701-702. doi: 10.1038/s41591-019-0391-9.
Nat Med. 2019.
PMID: 30787481
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Validation of a Single-Nucleotide Polymorphism-Based Non-Invasive Prenatal Test in Twin Gestations: Determination of Zygosity, Individual Fetal Sex, and Fetal Aneuploidy.
Norwitz ER, McNeill G, Kalyan A, Rivers E, Ahmed E, Meng L, Vu P, Egbert M, Shapira M, Kobara K, Parmar S, Goel S, Prins SA, Aruh I, Persico N, Robins JC, Kirshon B, Demko ZP, Ryan A, Billings PR, Rabinowitz M, Benn P, Martin KA, Hedriana HL.
Norwitz ER, et al. Among authors: parmar s.
J Clin Med. 2019 Jun 28;8(7):937. doi: 10.3390/jcm8070937.
J Clin Med. 2019.
PMID: 31261782
Free PMC article.
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