Molly Schroeder

1724

Citations

Research activity per year

Research interests

Dr. Schroeder is a clinical laboratory geneticist with boards in molecular genetics and cytogenetics. She is experienced in genomics, clinical assay development, and translational research.

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34 Article
4 Review article
2 Letter
1 Comment/debate

Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations
Ghasemi, R., Corliss, M. M., Bowling, K. M., Krysiak, K., Walker, J., Dickson, A. M., Schroeder, M. C., Parikh, B. A., Neidich, J. A., Polonis, K. & Cao, Y., Apr 2025, In: Clinical Genetics. 107, 4, p. 458-462 5 p.
Research output: Contribution to journal › Article › peer-review
1 Link opens in a new tab Scopus citations
Innovations in Short-Read Sequencing Technologies and Their Applications to Clinical Genomics
Polonis, K., Blommel, J. H., Hughes, A. E. O., Spencer, D., Thompson, J. A. & Schroeder, M. C., Jan 1 2025, In: Clinical chemistry. 71, 1, p. 97-108 12 p.
Research output: Contribution to journal › Review article › peer-review
9 Link opens in a new tab Scopus citations
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies
Küry, S., Stanton, J. E., van Woerden, G. M., Bosc-Rosati, A., Hsieh, T. C., Bray, L., Oloudé, M., Rosenfelt, C., Scott-Boyer, M. P., Most, V., Wang, T., Papendorf, J. J., de Konink, C., Deb, W., Vignard, V., Studencka-Turski, M., Besnard, T., Hajdukowicz, A. M., Thiel, F. G. & Wolfgramm, S. & 129 others, Florenceau, L., Cuinat, S., Marsac, S., Verrès, Y., Dangoumau, A., Poirier, L., Wentzensen, I. M., Tuttle, A., Forster, C., Striesow, J., Golnik, R., Ortiz, D., Jenkins, L., Rosenfeld, J. A., Ziegler, A., Houdayer, C., Bonneau, D., Torti, E., Begtrup, A., Monaghan, K. G., Mullegama, S. V., Volker-Touw, C. M. L. N., van Gassen, K. L. I., Oegema, R., de Pagter, M. S., Steindl, K., Rauch, A., Ivanovski, I., McDonald, K., Boothe, E., Dauber, A., Baker, J., Fabie, N. A. V., Bernier, R. A., Turner, T. N., Srivastava, S., Dies, K. A., Swanson, L. C., Costin, C., Abdulrazak, A., Jobling, R. K., Pappas, J., Rabin, R., Niyazov, D., Chun-Hui Tsai, A., Kovak, K., Beck, D. B., Malicdan, M. C. V., Adams, D. R., Wolfe, L., Ganetzky, R. D., Muraresku, C. C., Babikyan, D., Sedláček, Z., Hančárová, M., Timberlake, A. T., Saif, H. A., Nestler, B., King, K., Hajianpour, M. J., Costain, G., Prendergast, D., Li, C., Geneviève, D., Vitobello, A., Sorlin, A., Philippe, C., Harel, T., Toker, O., Sabir, A., Lim, D., Hamilton, M. J., Bryson, L. J., Cleary, E., Weber, S., Hoffman, T. L., Cueto-González, A. M., Tizzano, E. F., Gómez-Andrés, D., Codina-Solà, M., Ververi, A., Pavlidou, E., Lambropoulos, A., Garganis, K., Rio, M., Levy, J., Langas, S. J., McRae, A. M., Lessard, M. K., D’Agostino, M. D., De Bie, I., Wegler, M., Abou Jamra, R., Kamphausen, S. B., Bothe, V., Potocki, L., Olinger, E., Sznajer, Y., Wiame, E., Thompson, M. L., Schroeder, M. C., Gooch, C., Smith, R. A., Pandya, A., Busch, L. M., Völker, U., Hammer, E., Wende, K., Cogné, B., Isidor, B., Meiler, J., Ripoll, C., Bigou, S., Laumonnier, F., Hildebrand, P. W., Eichler, E. E., McWalter, K., Krawitz, P. M., Roux-Dalvai, F., Elgersma, Y., Marcoux, J., Bousquet, M. P., Droit, A., Poschmann, J., Grabrucker, A. M., Bolduc, F. V., Bézieau, S., Ebstein, F. & Krüger, E., Dec 2025, In: Nature communications. 16, 1, 10545.
Research output: Contribution to journal › Article › peer-review

Open Access
Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism
Leon-Quintero, F. Z., Bowling, K. M., Dickson, A., Corliss, M. M., Schroeder, M. C., Neidich, J. A., Heusel, J. W., Krysiak, K., Polonis, K., Parikh, B. A. & Cao, Y., Mar 2025, In: Clinical Genetics. 107, 3, p. 261-270 10 p.
Research output: Contribution to journal › Article › peer-review

Open Access
4 Link opens in a new tab Scopus citations
Novel t(14;19)(q32.2;p13.12) structural variant identified by genome sequencing in a myeloid neoplasm post cytotoxic therapy: a case report
Zhang, X., Claire Hou, Y. C., Duncavage, E. J., Spencer, D. H. & Schroeder, M. C., Oct 30 2025, In: Journal of Laboratory and Precision Medicine. 10, p. 1-6 6 p.
Research output: Contribution to journal › Article › peer-review

Molly Schroeder

Personal profile

Research interests

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Collaborations and top research areas from the last five years

Dive into details

Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations

Innovations in Short-Read Sequencing Technologies and Their Applications to Clinical Genomics

Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies

Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism

Novel t(14;19)(q32.2;p13.12) structural variant identified by genome sequencing in a myeloid neoplasm post cytotoxic therapy: a case report

Molly Schroeder

Personal profile

Research interests

Fingerprint

Collaborations and top research areas from the last five years

Research output

Comprehensive Analysis of TEK Variants in Patients With Vascular Malformations

Innovations in Short-Read Sequencing Technologies and Their Applications to Clinical Genomics

Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies

Modified Rules for Classification of Variants Associated With Disorders of Somatic Mosaicism

Novel t(14;19)(q32.2;p13.12) structural variant identified by genome sequencing in a myeloid neoplasm post cytotoxic therapy: a case report