Genetics at BMC
@OAgenetics
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A group of Open Access journals highlighting cutting edge research in the genetics sector. Published by BioMed Central - a part of Springer Nature.
Joined October 2010
👓Read a new article on Knowledge mapping and bibliometric insights into gene therapy for rare inherited hematologic pathologies: focus on sickle cell disease, hemophilia, and thalassemia. ➡️ https://t.co/NMDv5DQ4NL
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🧫Call for Content: Don't forget to submit to Biological Procedures Online's new Collection 'Current and novel therapeutic approaches to gastrointestinal cancers'! Guest Edited by Dr Kelley Núñez' https://t.co/mZl0eS3jkh
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🆕New research published in Orphanet Journal of Rare Diseases GRIN2B-related neurodevelopmental disorders: genotype-phenotype correlations and therapeutic implications ➡️ https://t.co/a2qEMp4mHX
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🧬A study in Epigenetics Communications examines D-loop methylation and mtDNA copy number in individuals with Down syndrome The results show no significant differences compared to controls ➡️ https://t.co/2HDmATxafX
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🩻Call for Content: Don't forget to submit to Skeletal Muscle's new Collection 'Molecular mechanisms in skeletal muscle: insights into development, regeneration, and maintenance'! Guest Edited by Dr Hang Yin https://t.co/z7kAcNb4jx
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COLLECTION OPEN Algorithms for Molecular Biology is calling for papers on 'Machine Learning and Artificial Intelligence for Sequence Analysis' Read more and submit: https://t.co/jSmpugK6Ki
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Call for Content: New Collection launched focusing on Optical Genome Mapping in Deciphering Genetic Diseases. Submissions welcome! https://t.co/HgM6iO1nOD
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🆕A new study in Genes & Nutrition highlights the potential utility of PRS-EA in assessing and managing NAFLD risk, particularly in individuals with lipid metabolic dysfunction and hypertension. ➡️ https://t.co/nSEA1YGvrz
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Listen to a podcast exploring the intersection of race, maternal mental health and healthcare inequality with Dr Irene Aninye and Publisher, India Sapsed-Foster for Black Maternal Mental Health Week 2025 @BiolSexDiff
@SWHR
@OSSDtweets
https://t.co/Yy9RugdsII
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💡Call for Content💡 New Collection launched focusing on Climate Change and Its Impact on the Genome and Epigenome. Submissions welcome! https://t.co/beL1N41Dka
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Read a new article in Orphanet Journal of Rare Diseases: The neurologic face of X-linked lymphoproliferative syndrome type 1: a systematic review. ➡️ https://t.co/gjkcQ24ldD
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A new Study in Clinical Epigenetics: Epigenetic mediation may explain intergenerational associations between maternal obesogenic lifestyle and children’s birth weight: findings from the NorthPop prospective birth cohort. ➡️ https://t.co/81nWhaKxpI
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Call for Content: Don't forget to submit to Biology of Sex Differences' collection 'Sex differences in neurodegenerative diseases! Guest Edited by Lisa S. Robison. https://t.co/o5Fr3MRWFI
@SWHR @OSSDtweets @BiolSexDiff
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Read a new research article about DNA methylation profiles and cancer in children conceived after assisted reproductive technology. ➡️ https://t.co/ggc9FTSGxF
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Read a new article in Genes & Nutrition: Association of dietary total antioxidant capacity with KRAS gene mutation in metastatic colorectal cancer patients: a case-control study. ➡️ https://t.co/suEQZHkxzc
genesandnutrition.biomedcentral.com
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Check out Skeletal Muscle's Featured Review: Signaling networks governing skeletal muscle growth, atrophy, and cachexia @ashokkmann @UH_Pharmacy @meiri_tomaz ➡️ https://t.co/DekglF67Ev
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This study investigated the clinical and genetic characteristics of patients with chronic sinopulmonary symptoms in northern Vietnam, focusing on individuals with a strong suspicion of hereditary involvement to identify causative genes. https://t.co/gfmbgcy7bO
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The Orphanet Journal of Rare Diseases reviews hypophosphatemic disorders, focusing on X-linked hypophosphatemia (XLH) and tumor-induced osteomalacia (TIO), both linked to excess FGF23 causing phosphate wasting. ➡️ https://t.co/F08zpC5164
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New EWAS study links serum copper levels to DNA methylation changes that may influence risk of type 2 diabetes and cardiovascular disease. Epigenetics offers fresh insight into trace element–disease connections. #Epigenetics #T2D #CVD #Copper ➡️ https://t.co/j9tuOFe5oz
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COLLECTION OPEN Algorithms for Molecular Biology is calling for papers on 'Machine Learning and Artificial Intelligence for Sequence Analysis' Read more and submit: https://t.co/jSmpugK6Ki
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