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Showing 229 to 235 of 235 entries
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Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities.

Frontiers in public health

Hirsch JA, Meyer KA, Peterson M, Rodriguez DA, Song Y, Peng K, Huh J, Gordon-Larsen P.
PMID: 27148512
Front Public Health. 2016 Apr 19;4:65. doi: 10.3389/fpubh.2016.00065. eCollection 2016.

BACKGROUND: Neighborhood transportation infrastructure and public recreational facilities are theorized to improve the activity, weight, and cardiometabolic profiles of individuals living in close proximity to these resources. However, owing to data limitations, there has not been adequate study of...

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Hirsch JA, Meyer KA, Peterson M, et al. Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities. Front Public Health. 2016;4:65doi: 10.3389/fpubh.2016.00065.
Hirsch, J. A., Meyer, K. A., Peterson, M., Rodriguez, D. A., Song, Y., Peng, K., Huh, J., & Gordon-Larsen, P. (2016). Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities. Frontiers in public health, 465. https://doi.org/10.3389/fpubh.2016.00065
Hirsch, Jana A, et al. "Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities." Frontiers in public health vol. 4 (2016): 65. doi: https://doi.org/10.3389/fpubh.2016.00065
Hirsch JA, Meyer KA, Peterson M, Rodriguez DA, Song Y, Peng K, Huh J, Gordon-Larsen P. Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities. Front Public Health. 2016 Apr 19;4:65. doi: 10.3389/fpubh.2016.00065. eCollection 2016. PMID: 27148512; PMCID: PMC4835448.
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Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities.

Frontiers in public health

Hirsch JA, Meyer KA, Peterson M, Rodriguez DA, Song Y, Peng K, Huh J, Gordon-Larsen P.
PMID: 27148512
Front Public Health. 2016 Apr 19;4:65. doi: 10.3389/fpubh.2016.00065. eCollection 2016.

BACKGROUND: Neighborhood transportation infrastructure and public recreational facilities are theorized to improve the activity, weight, and cardiometabolic profiles of individuals living in close proximity to these resources. However, owing to data limitations, there has not been adequate study of...

Cite
Hirsch JA, Meyer KA, Peterson M, et al. Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities. Front Public Health. 2016;4:65doi: 10.3389/fpubh.2016.00065.
Hirsch, J. A., Meyer, K. A., Peterson, M., Rodriguez, D. A., Song, Y., Peng, K., Huh, J., & Gordon-Larsen, P. (2016). Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities. Frontiers in public health, 465. https://doi.org/10.3389/fpubh.2016.00065
Hirsch, Jana A, et al. "Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities." Frontiers in public health vol. 4 (2016): 65. doi: https://doi.org/10.3389/fpubh.2016.00065
Hirsch JA, Meyer KA, Peterson M, Rodriguez DA, Song Y, Peng K, Huh J, Gordon-Larsen P. Obtaining Longitudinal Built Environment Data Retrospectively across 25 years in Four US Cities. Front Public Health. 2016 Apr 19;4:65. doi: 10.3389/fpubh.2016.00065. eCollection 2016. PMID: 27148512; PMCID: PMC4835448.
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Relationships among Inorganic Arsenic, Nutritional Status CpG Methylation and microRNAs: A Review of the Literature.

Epigenetics insights

Venkatratnam A, Marable CA, Keshava AM, Fry RC.
PMID: 33615137
Epigenet Insights. 2021 Feb 05;14:2516865721989719. doi: 10.1177/2516865721989719. eCollection 2021.

Inorganic arsenic is a naturally occurring toxicant that poses a significant and persistent challenge to public health. The World Health Organization has identified many geographical regions where inorganic arsenic levels exceed safe limits in drinking water. Numerous epidemiological studies...

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Venkatratnam A, Marable CA, Keshava AM, et al. Relationships among Inorganic Arsenic, Nutritional Status CpG Methylation and microRNAs: A Review of the Literature. Epigenet Insights. 2021;14:2516865721989719doi: 10.1177/2516865721989719.
Venkatratnam, A., Marable, C. A., Keshava, A. M., & Fry, R. C. (2021). Relationships among Inorganic Arsenic, Nutritional Status CpG Methylation and microRNAs: A Review of the Literature. Epigenetics insights, 142516865721989719. https://doi.org/10.1177/2516865721989719
Venkatratnam, Abhishek, et al. "Relationships among Inorganic Arsenic, Nutritional Status CpG Methylation and microRNAs: A Review of the Literature." Epigenetics insights vol. 14 (2021): 2516865721989719. doi: https://doi.org/10.1177/2516865721989719
Venkatratnam A, Marable CA, Keshava AM, Fry RC. Relationships among Inorganic Arsenic, Nutritional Status CpG Methylation and microRNAs: A Review of the Literature. Epigenet Insights. 2021 Feb 05;14:2516865721989719. doi: 10.1177/2516865721989719. eCollection 2021. PMID: 33615137; PMCID: PMC7868494.
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Clustering Longitudinal Blood Pressure Trajectories to Examine Heterogeneity in Outcomes Among Preeclampsia Cases and Controls.

Hypertension (Dallas, Tex. : 1979)

Roell KR, Harmon QE, Klungsøyr K, Bauer AE, Magnus P, Engel SM.
PMID: 33813841
Hypertension. 2021 Jun;77(6):2034-2044. doi: 10.1161/HYPERTENSIONAHA.120.16239. Epub 2021 Apr 05.

[Figure: see text].

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Roell KR, Harmon QE, Klungsøyr K, et al. Clustering Longitudinal Blood Pressure Trajectories to Examine Heterogeneity in Outcomes Among Preeclampsia Cases and Controls. Hypertension. 2021;77(6):2034-2044doi: 10.1161/HYPERTENSIONAHA.120.16239.
Roell, K. R., Harmon, Q. E., Klungsøyr, K., Bauer, A. E., Magnus, P., & Engel, S. M. (2021). Clustering Longitudinal Blood Pressure Trajectories to Examine Heterogeneity in Outcomes Among Preeclampsia Cases and Controls. Hypertension (Dallas, Tex. : 1979), 77(6), 2034-2044. https://doi.org/10.1161/HYPERTENSIONAHA.120.16239
Roell, Kyle R, et al. "Clustering Longitudinal Blood Pressure Trajectories to Examine Heterogeneity in Outcomes Among Preeclampsia Cases and Controls." Hypertension (Dallas, Tex. : 1979) vol. 77,6 (2021): 2034-2044. doi: https://doi.org/10.1161/HYPERTENSIONAHA.120.16239
Roell KR, Harmon QE, Klungsøyr K, Bauer AE, Magnus P, Engel SM. Clustering Longitudinal Blood Pressure Trajectories to Examine Heterogeneity in Outcomes Among Preeclampsia Cases and Controls. Hypertension. 2021 Jun;77(6):2034-2044. doi: 10.1161/HYPERTENSIONAHA.120.16239. Epub 2021 Apr 05. PMID: 33813841; PMCID: PMC8119318.
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Case-cohort design in hematopoietic cell transplant studies.

Bone marrow transplantation

Cai J, Kim S.
PMID: 34400795
Bone Marrow Transplant. 2022 Jan;57(1):1-5. doi: 10.1038/s41409-021-01433-4. Epub 2021 Aug 16.

SERIES EDITORS- NOTE: Imagine you and your colleagues have done 1000 transplants in persons with acute myeloid leukaemia (AML) in 1st remission. 5 percent of the 20 percent of recipients relapsing posttransplant have an isolated central nervous system relapse....

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Cai J, Kim S. Case-cohort design in hematopoietic cell transplant studies. Bone Marrow Transplant. 2021;57(1):1-5doi: 10.1038/s41409-021-01433-4.
Cai, J., & Kim, S. (2022). Case-cohort design in hematopoietic cell transplant studies. Bone marrow transplantation, 57(1), 1-5. https://doi.org/10.1038/s41409-021-01433-4
Cai, Jianwen, and Kim, Soyoung. "Case-cohort design in hematopoietic cell transplant studies." Bone marrow transplantation vol. 57,1 (2022): 1-5. doi: https://doi.org/10.1038/s41409-021-01433-4
Cai J, Kim S. Case-cohort design in hematopoietic cell transplant studies. Bone Marrow Transplant. 2022 Jan;57(1):1-5. doi: 10.1038/s41409-021-01433-4. Epub 2021 Aug 16. PMID: 34400795; PMCID: PMC8738130.
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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

Genome medicine

Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A, Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K, Earl RK, Nowakowski T, Bernier RA, Eichler EE.
PMID: 33874999
Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6.

BACKGROUND: With the increasing number of genomic sequencing studies, hundreds of genes have been implicated in neurodevelopmental disorders (NDDs). The rate of gene discovery far outpaces our understanding of genotype-phenotype correlations, with clinical characterization remaining a bottleneck for understanding...

Cite
Gillentine MA, Wang T, Hoekzema K, et al. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome Med. 2021;13(1):63doi: 10.1186/s13073-021-00870-6.
Gillentine, M. A., Wang, T., Hoekzema, K., Rosenfeld, J., Liu, P., Guo, H., Kim, C. N., De Vries, B. B. A., Vissers, L. E. L. M., Nordenskjold, M., Kvarnung, M., Lindstrand, A., Nordgren, A., Gecz, J., Iascone, M., Cereda, A., Scatigno, A., Maitz, S., Zanni, G., Bertini, E., Zweier, C., Schuhmann, S., Wiesener, A., Pepper, M., Panjwani, H., Torti, E., Abid, F., Anselm, I., Srivastava, S., Atwal, P., Bacino, C. A., Bhat, G., Cobian, K., Bird, L. M., Friedman, J., Wright, M. S., Callewaert, B., Petit, F., Mathieu, S., Afenjar, A., Christensen, C. K., White, K. M., Elpeleg, O., Berger, I., Espineli, E. J., Fagerberg, C., Brasch-Andersen, C., Hansen, L. K., Feyma, T., Hughes, S., Thiffault, I., Sullivan, B., Yan, S., Keller, K., Keren, B., Mignot, C., Kooy, F., Meuwissen, M., Basinger, A., Kukolich, M., Philips, M., Ortega, L., Drummond-Borg, M., Lauridsen, M., Sorensen, K., Lehman, A., Lopez-Rangel, E., Levy, P., Lessel, D., Lotze, T., Madan-Khetarpal, S., Sebastian, J., Vento, J., Vats, D., Benman, L. M., Mckee, S., Mirzaa, G. M., Muss, C., Pappas, J., Peeters, H., Romano, C., Elia, M., Galesi, O., Simon, M. E. H., van Gassen, K. L. I., Simpson, K., Stratton, R., Syed, S., Thevenon, J., Palafoll, I. V., Vitobello, A., Bournez, M., Faivre, L., Xia, K., Earl, R. K., Nowakowski, T., Bernier, R. A., & Eichler, E. E. (2021). Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome medicine, 13(1), 63. https://doi.org/10.1186/s13073-021-00870-6
Gillentine, Madelyn A, et al. "Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders." Genome medicine vol. 13,1 (2021): 63. doi: https://doi.org/10.1186/s13073-021-00870-6
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A, Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K, Earl RK, Nowakowski T, Bernier RA, Eichler EE. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6. PMID: 33874999; PMCID: PMC8056596.
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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.

Genome medicine

Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A, Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K, Earl RK, Nowakowski T, Bernier RA, Eichler EE.
PMID: 33874999
Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6.

BACKGROUND: With the increasing number of genomic sequencing studies, hundreds of genes have been implicated in neurodevelopmental disorders (NDDs). The rate of gene discovery far outpaces our understanding of genotype-phenotype correlations, with clinical characterization remaining a bottleneck for understanding...

Cite
Gillentine MA, Wang T, Hoekzema K, et al. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome Med. 2021;13(1):63doi: 10.1186/s13073-021-00870-6.
Gillentine, M. A., Wang, T., Hoekzema, K., Rosenfeld, J., Liu, P., Guo, H., Kim, C. N., De Vries, B. B. A., Vissers, L. E. L. M., Nordenskjold, M., Kvarnung, M., Lindstrand, A., Nordgren, A., Gecz, J., Iascone, M., Cereda, A., Scatigno, A., Maitz, S., Zanni, G., Bertini, E., Zweier, C., Schuhmann, S., Wiesener, A., Pepper, M., Panjwani, H., Torti, E., Abid, F., Anselm, I., Srivastava, S., Atwal, P., Bacino, C. A., Bhat, G., Cobian, K., Bird, L. M., Friedman, J., Wright, M. S., Callewaert, B., Petit, F., Mathieu, S., Afenjar, A., Christensen, C. K., White, K. M., Elpeleg, O., Berger, I., Espineli, E. J., Fagerberg, C., Brasch-Andersen, C., Hansen, L. K., Feyma, T., Hughes, S., Thiffault, I., Sullivan, B., Yan, S., Keller, K., Keren, B., Mignot, C., Kooy, F., Meuwissen, M., Basinger, A., Kukolich, M., Philips, M., Ortega, L., Drummond-Borg, M., Lauridsen, M., Sorensen, K., Lehman, A., Lopez-Rangel, E., Levy, P., Lessel, D., Lotze, T., Madan-Khetarpal, S., Sebastian, J., Vento, J., Vats, D., Benman, L. M., Mckee, S., Mirzaa, G. M., Muss, C., Pappas, J., Peeters, H., Romano, C., Elia, M., Galesi, O., Simon, M. E. H., van Gassen, K. L. I., Simpson, K., Stratton, R., Syed, S., Thevenon, J., Palafoll, I. V., Vitobello, A., Bournez, M., Faivre, L., Xia, K., Earl, R. K., Nowakowski, T., Bernier, R. A., & Eichler, E. E. (2021). Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome medicine, 13(1), 63. https://doi.org/10.1186/s13073-021-00870-6
Gillentine, Madelyn A, et al. "Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders." Genome medicine vol. 13,1 (2021): 63. doi: https://doi.org/10.1186/s13073-021-00870-6
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A, Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K, Earl RK, Nowakowski T, Bernier RA, Eichler EE. Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders. Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6. PMID: 33874999; PMCID: PMC8056596.
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Showing 229 to 235 of 235 entries