What are the markers of aggressiveness in prolactinomas? Changes in cell biology, extracellular matrix components, angiogenesis and genetics. by Gürlek, A, Karavitaki, N, Ansorge, O, Wass, J

The role of chemokines in atherosclerosis: recent evidence from experimental models and population genetics. by Bursill, C, Channon, K, Greaves, D

Toward an interactive article: integrating journals and biological databases by Marygold Steven J, Skrzypek Marek S, Isaacson Ruth, DePellegrin-Connelly Tracey, Faelten Sharon, Otis Lolly, Haenel Stephen, Chan Juancarlos, Yook Karen, Schedl Tim, Rangarajan Arun, Stefancsik Raymund, Cherry J, Sternberg Paul W, Müller Hans-Michael

“…</p> <p>Results</p> <p>We have established a journal article mark-up pipeline that links GENETICS journal articles and the model organism database (MOD) WormBase. …”
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10 Years of Toxicogenomics section in Frontiers in Genetics: Past discoveries and Future Perspectives by Douglas M. Ruden

“…The year 2021 was the 10th anniversary of the founding of the Frontiers in Genetics journal and the Frontiers in Toxicogenomics specialty section of this journal. …”
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Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. by Beaumont, RN, Warrington, NM, Cavadino, A, Tyrrell, J, Nodzenski, M, Horikoshi, M, Geller, F, Myhre, R, Richmond, RC, Paternoster, L, Bradfield, JP, Kreiner-Møller, E, Huikari, V, Metrustry, S, Lunetta, KL, Painter, JN, Hottenga, J-J, Allard, C, Barton, SJ, Espinosa, A, Marsh, JA, Potter, C, Zhang, G, Ang, W, Berry, DJ, Bouchard, L, Das, S, Hakonarson, H, Heikkinen, J, Helgeland, Ø, Hocher, B, Hofman, A, Inskip, HM, Jones, SE, Kogevinas, M, Lind, PA, Marullo, L, Medland, SE, Murray, A, Murray, JC, Njølstad, PR, Nohr, EA, Reichetzeder, C, Ring, SM, Ruth, KS, Santa-Marina, L, Scholtens, DM, Sebert, S, Sengpiel, V, Tuke, MA, Vaudel, M, Weedon, MN, Willemsen, G, Wood, AR, Yaghootkar, H, Muglia, LJ, Bartels, M, Relton, CL, Pennell, CE, Chatzi, L, Estivill, X, Holloway, JW, Boomsma, DI, Montgomery, GW, Murabito, JM, Spector, TD, Power, C, Järvelin, M-R, Bisgaard, H, Grant, SF, Sørensen, TI, Jaddoe, VW, Jacobsson, B, Melbye, M, McCarthy, MI, Hattersley, AT, Hayes, MG, Frayling, TM, Hivert, M-F, Felix, JF, Hyppönen, E, Lowe, WL, Evans, DM, Lawlor, DA, Feenstra, B, Freathy, RM

Non-invasive preimplantation genetic testing (niPGT): the next revolution in reproductive genetics? by Leaver, M, Wells, D

Illumina next generation sequencing data and expression microarrays data from retinoblastoma and medulloblastoma tissues by A.J. García-Chequer, A. Méndez-Tenorio, G. Olguín-López, C. Sánchez-Vallejo, P. Isa, C.F. Arias, J. Torres, A. Hernández-Angeles, M.A. Ramírez-Ortiz, C. Lara, Ma.de.L. Cabrera-Muñoz, S. Sadowinski-Pine, J.C. Bravo-Ortiz, G. Ramón-García, J. Diegopérez-Ramírez, G. Ramírez-Reyes, R. Casarrubias-Islas, J. Ramírez, M. Orjuela, M.V. Ponce-Castañeda

“…The complete research article can be found at Cancer Genetics journal (Garcia-Chequer et al., in press) [1]. …”
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Microbial Diversity and Flavor Substance Changes of Vinegar Based on Cite Space Visualization Analysis Technology by Xiaoting YE, Jiaxin LIU, Yongjian YU, Yuanyuan ZHU, Zhen YU, Dong HAN, Peng LIU, Yuqin WANG, Ke WANG

“…The changes of knowledge flow in this research area were mainly from science, molecular, biology, immunology journals to environmental, toxicology, nutrition, molecular biology, genetics journals. Dynamics, solid state fermentation and volatile compounds would become new research hot spots.…”
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Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions by Ali AlMail, Ahmed Jamjoom, Amy Pan, Min Yi Feng, Vann Chau, Alissa M. D’Gama, Katherine Howell, Nicole S. Y. Liang, Amy McTague, Annapurna Poduri, Kimberly Wiltrout, IPCHiP Executive Committee, Anne S. Bassett, John Christodoulou, Lucie Dupuis, Peter Gill, Tess Levy, Paige Siper, Zornitza Stark, Jacob A. S. Vorstman, Catherine Diskin, Natalie Jewitt, Danielle Baribeau, Gregory Costain

“…We identified reports published from 2017 to 2021 in 10 genetics journals of novel Mendelian disorders. We adjudicated the quality and detail of the phenotype data via 46 questions pertaining to six priority domains: (I) Development, cognition, and mental health; (II) Feeding and growth; (III) Medication use and treatment history; (IV) Pain, sleep, and quality of life; (V) Adulthood; and (VI) Epilepsy. …”
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Pour une lecture Girardienne des Bonnes de Genet by Killeen, M