Jaclyn Murry

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14 Article
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Live-Born Double Aneuploidy at the Johns Hopkins Cytogenomics Laboratory: Case Report and Review of the Literature
Murry, J. B. & Zou, Y. S., 2022, In: OBM Genetics. 6, 4
Research output: Contribution to journal › Article › peer-review

Open Access
Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study
The BabySeq Project Team, Apr 27 2022, In: Frontiers in Genetics. 13, 867371.
Research output: Contribution to journal › Article › peer-review

Open Access
Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences
Bi, W., Yuan, B., Liu, P., Murry, J. B., Qin, X., Xia, F., Quach, T., Cooper, L. M., Wiszniewska, J., Hixson, P., Peacock, S., Tonk, V. S., Huff, R. W., Ortega, V., Lupski, J. R., Scherer, S. E., Littlejohn, R. O., Velagaleti, G. V. N., Roeder, E. R. & Cheung, S. W., 2022, (Accepted/In press) In: Journal of medical genetics. 108586.
Research output: Contribution to journal › Article › peer-review
Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project
BabySeq Project Team, Jul 2021, In: Genetics in Medicine. 23, 7, p. 1372-1375 4 p.
Research output: Contribution to journal › Article › peer-review

Open Access
Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders
Mannucci, I., Dang, N. D. P., Huber, H., Murry, J. B., Abramson, J., Althoff, T., Banka, S., Baynam, G., Bearden, D., Beleza-Meireles, A., Benke, P. J., Berland, S., Bierhals, T., Bilan, F., Bindoff, L. A., Braathen, G. J., Busk, Ø. L., Chenbhanich, J., Denecke, J., Escobar, L. F., & 45 othersEstes, C., Fleischer, J., Groepper, D., Haaxma, C. A., Hempel, M., Holler-Managan, Y., Houge, G., Jackson, A., Kellogg, L., Keren, B., Kiraly-Borri, C., Kraus, C., Kubisch, C., Le Guyader, G., Ljungblad, U. W., Brenman, L. M., Martinez-Agosto, J. A., Might, M., Miller, D. T., Minks, K. Q., Moghaddam, B., Nava, C., Nelson, S. F., Parant, J. M., Prescott, T., Rajabi, F., Randrianaivo, H., Reiter, S. F., Schuurs-Hoeijmakers, J., Shieh, P. B., Slavotinek, A., Smithson, S., Stegmann, A. P. A., Tomczak, K., Tveten, K., Wang, J., Whitlock, J. H., Zweier, C., McWalter, K., Juusola, J., Quintero-Rivera, F., Fischer, U., Yeo, N. C., Kreienkamp, H. J. & Lessel, D., Dec 2021, In: Genome Medicine. 13, 1, 90.
Research output: Contribution to journal › Article › peer-review

Open Access

Jaclyn Murry

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Live-Born Double Aneuploidy at the Johns Hopkins Cytogenomics Laboratory: Case Report and Review of the Literature

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences

Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project

Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

Jaclyn Murry

Fingerprint

Network

Research output

Live-Born Double Aneuploidy at the Johns Hopkins Cytogenomics Laboratory: Case Report and Review of the Literature

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences

Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project

Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders