Institute for Personalized Medicine

Websitehttps://research.med.psu.edu/departments/personalized-medicine

Postal addressShow on map
500 University Drive
17033 Hershey
United States

53947 Citations
101 h-index
432 Article
23 Review article
11 Comment/debate
10 Conference contribution
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9 results

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2023

Odds of Cardiometabolic Diseases and Medications in Children With Cerebral Palsy
Dum, R., Walter, V., Thomas, N. J. & Krawiec, C., Mar 2023, In: Journal of Child Neurology. 38, 3-4, p. 239-246 8 p.
Research output: Contribution to journal › Letter › peer-review
2021

Authors’ Reply: To the Letter to the Editor by Kessel et al
Stoltzfus, K. C., Shen, B., Tchelebi, L., Trifiletti, D. M., Gusani, N. J., Walter, V., Wang, M. & Zaorsky, N. G., Jul 2021, In: JNCCN Journal of the National Comprehensive Cancer Network. 19, 7, p. XLIII-XLIV
Research output: Contribution to journal › Letter › peer-review

Open Access
Increased Incidence of IKZF1 deletions and IGH-CRLF2 translocations in B-ALL of Hispanic/Latino children—a novel health disparity
Raca, G., Abdel-Azim, H., Yue, F., Broach, J., Payne, J. L., Reeves, M. E., Gowda, C., Schramm, J., Desai, D., Dovat, E., Hu, T., Berg, A. S., Bhojwani, D., Payne, K. J. & Dovat, S., Aug 2021, In: Leukemia. 35, 8, p. 2399-2402 4 p.
Research output: Contribution to journal › Letter › peer-review

Open Access

23 Scopus citations
Prothrombotic variants as modifiers of clinical phenotype in four related individuals with haemophilia A
Carrel, L., Arnold-Croop, S., Achtermann, T., Chen, F., Cheng, Y., Liu, D. & Eyster, M. E., Jul 2021, In: Haemophilia. 27, 4, p. e591-e595
Research output: Contribution to journal › Letter › peer-review
2020

Investigation of discordant phenotype in mild Hemophilia A using whole exome sequencing
Cygan, P. H., Arnold-Croop, S. E., Weidman, E. A., Chen, F., Liu, D. J., Eyster, M. E. & Carrel, L., Sep 2020, In: Thrombosis Research. 193, p. 36-39 4 p.
Research output: Contribution to journal › Letter › peer-review

1 Scopus citations
2019
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
23andMe Research Team, HUNT All-In Psychiatry, Liu, M., Jiang, Y., Wedow, R., Li, Y., Brazel, D. M., Chen, F., Datta, G., Davila-Velderrain, J., McGuire, D., Tian, C., Zhan, X., Agee, M., Alipanahi, B., Auton, A., Bell, R. K., Bryc, K., Elson, S. L. & Fontanillas, P. & 32 others, Furlotte, N. A., Hinds, D. A., Hromatka, B. S., Huber, K. E., Kleinman, A., Litterman, N. K., McIntyre, M. H., Mountain, J. L., Northover, C. A. M., Sathirapongsasuti, J. F., Sazonova, O. V., Shelton, J. F., Shringarpure, S., Tian, C., Tung, J. Y., Vacic, V., Wilson, C. H., Pitts, S. J., Mitchell, A., Skogholt, A. H., Winsvold, B. S., Sivertsen, B., Stordal, E., Morken, G., Kallestad, H., Heuch, I., Zwart, J. A., Fjukstad, K. K., Pedersen, L. M., Gabrielsen, M. E., Johnsen, M. B. & Liu, D., Feb 1 2019, In: Nature Genetics. 51, 2, p. 237-244 8 p.
Research output: Contribution to journal › Letter › peer-review

Open Access
1164 Scopus citations
2016

Covariance estimators for Generalized Estimating Equations (GEE) in longitudinal analysis with small samples
Wang, M., Kong, L., Li, Z. & Zhang, L., Dec 10 2016, In: Statistics in Medicine. 35, 28, p. 5318-5319 2 p.
Research output: Contribution to journal › Letter › peer-review

3 Scopus citations
2013
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
Zhan, X., Larson, D. E., Wang, C., Koboldt, D. C., Sergeev, Y. V., Fulton, R. S., Fulton, L. L., Fronick, C. C., Branham, K. E., Bragg-Gresham, J., Jun, G., Hu, Y., Kang, H. M., Liu, D., Othman, M., Brooks, M., Ratnapriya, R., Boleda, A., Grassmann, F. & Von Strachwitz, C. & 40 others, Olson, L. M., Buitendijk, G. H. S., Hofman, A., Van Duijn, C. M., Cipriani, V., Moore, A. T., Shahid, H., Jiang, Y., Conley, Y. P., Morgan, D. J., Kim, I. K., Johnson, M. P., Cantsilieris, S., Richardson, A. J., Guymer, R. H., Luo, H., Ouyang, H., Licht, C., Pluthero, F. G., Zhang, M. M., Zhang, K., Baird, P. N., Blangero, J., Klein, M. L., Farrer, L. A., DeAngelis, M. M., Weeks, D. E., Gorin, M. B., Yates, J. R. W., Klaver, C. C. W., Pericak-Vance, M. A., Haines, J. L., Weber, B. H. F., Wilson, R. K., Heckenlively, J. R., Chew, E. Y., Stambolian, D., Mardis, E. R., Swaroop, A. & Abecasis, G. R., Nov 2013, In: Nature Genetics. 45, 11, p. 1375-1381 7 p.
Research output: Contribution to journal › Letter › peer-review

Open Access
139 Scopus citations
2012
An encyclopedia of mouse DNA elements (Mouse ENCODE)
Stamatoyannopoulos, J. A., Snyder, M., Hardison, R., Ren, B., Gingeras, T., Gilbert, D. M., Groudine, M., Bender, M., Kaul, R., Canfield, T., Giste, E., Johnson, A., Zhang, M., Balasundaram, G., Byron, R., Roach, V., Sabo, P. J., Sandstrom, R., Stehling, A. S. & Thurman, R. E. & 66 others, Weissman, S. M., Cayting, P., Hariharan, M., Lian, J., Cheng, Y., Landt, S. G., Ma, Z., Wold, B. J., Dekker, J., Crawford, G. E., Keller, C. A., Wu, W., Morrissey, C., Kumar, S. A., Mishra, T., Jain, D., Byrska-Bishop, M., Blankenberg, D., Lajoiel, B. R., Jain, G., Sanyal, A., Chen, K. B., Denas, O., Taylor, J., Blobel, G. A., Weiss, M. J., Pimkin, M., Deng, W., Marinov, G. K., Williams, B. A., Fisher-Aylor, K. I., Desalvo, G., Kiralusha, A., Trout, D., Amrhein, H., Mortazavi, A., Edsall, L., McCleary, D., Kuan, S., Shen, Y., Yue, F., Ye, Z., Davis, C. A., Zaleski, C., Jha, S., Xue, C., Dobin, A., Lin, W., Fastuca, M., Wang, H., Guigo, R., Djebali, S., Lagarde, J., Ryba, T., Sasaki, T., Malladi, V. S., Cline, M. S., Kirkup, V. M., Learned, K., Rosenbloom, K. R., Kent, W. J., Feingold, E. A., Good, P. J., Pazin, M., Lowdon, R. F. & Adams, L. B., Aug 13 2012, In: Genome biology. 13, 8, 418.
Research output: Contribution to journal › Letter › peer-review

Open Access
356 Scopus citations

Institute for Personalized Medicine

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