Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 427 Records) |
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| Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). medRxiv : the preprint server for health sciences 2023 12 . Jessica H Hall, Samuel J R A Chawner, , Jeanne Wolstencroft, David Skuse, Peter Holmans, Michael J Owen, Marianne B M van den Br |
| Unraveling the Universality of Chemical Fear Communication: Evidence from Behavioral, Genetic, and Chemical Analyses. Chemical senses 2023 11 . Jasper H B de Groot, Tobias Haertl, Helene M Loos, Christin Bachmann, Athanasia Kontouli, Monique A M Smee |
| Identification of Neurotransmission and Synaptic Biological Processes Disrupted in Autism Spectrum Disorder Using Interaction Networks and Community Detection Analysis. Biomedicines 2023 11 11 (11): . Joana Vilela, Hugo Martiniano, Ana Rita Marques, João Xavier Santos, Muhammad Asif, Célia Rasga, Guiomar Oliveira, Astrid Moura Vicen |
| Uncovering convergence and divergence between autism and schizophrenia using genomic tools and patients' neurons. Molecular psychiatry 2024 9 . Eva Romanovsky, Ashwani Choudhary, David Peles, Ahmad Abu-Akel, Shani Ste |
| Dissection of the cell communication interactions in lung adenocarcinoma identified a prognostic model with immunotherapy efficacy assessment and a potential therapeutic candidate gene ITGB1. Heliyon 2024 9 10 (17): e36599. Xing Jin, Zhengyang Hu, Jiacheng Yin, Guangyao Shan, Mengnan Zhao, Zhenyu Liao, Jiaqi Liang, Guoshu Bi, Ye Cheng, Junjie Xi, Zhencong Chen, Miao L |
| Overlapping hearing and communication profiles for the deletion and the RAI1 variant form of Smith-Magenis Syndrome (SMS). Journal of communication disorders 2024 8 111 106455. Christine Brennan, Rachael R Baid |
| Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication. medRxiv : the preprint server for health sciences 2024 8 . Xiaojie Zhao, Yan Li, Siwei Zhang, Ari Sudwarts, Hanwen Zhang, Alena Kozlova, Matthew J Moulton, Lindsey D Goodman, Zhiping P Pang, Alan R Sanders, Hugo J Bellen, Gopal Thinakaran, Jubao Du |
| Short communication: catechol-O-methyltransferase allelic variation in relation to psychological and hormonal indices of stress in children and adolescents with chromosome 22q11.2 deletion syndrome (22q11.2DS). Journal of applied genetics 2024 8 . Jessie L Beebe, Cydney R Martin, Ashley F P Sanders, Jeremy Guidry, Fahad Faheem, Joel Atallah, Elliott A Beat |
| A novel CAF-cancer cell crosstalk-related gene prognostic index based on machine learning: prognostic significance and prediction of therapeutic response in head and neck squamous cell carcinoma. Journal of translational medicine 2024 7 22 (1): 645. Yuming Xu, Junda Li, Jinming Wang, Feilong De |
| Co-Occurring Methylenetetrahydrofolate Reductase (MTHFR) rs1801133 and rs1801131 Genotypes as Associative Genetic Modifiers of Clinical Severity in Rett Syndrome. Brain sciences 2024 7 14 (7): . Jatinder Singh, Georgina Wilkins, Ella Goodman-Vincent, Samiya Chishti, Ruben Bonilla Guerrero, Leighton McFadden, Zvi Zahavi, Paramala Santo |
| Rare Pathogenic Variants Identified in Whole Exome Sequencing of Monozygotic Twins With Autism Spectrum Disorder. Pediatric neurology 2024 7 158 113-123. Ayyappan Anitha, Moinak Banerjee, Ismail Thanseem, Anil Prakash, Nisha Melempatt, P S Sumitha, Mary Iype, Sanjeev V Thom |
| A scientometric study on research trends and characteristics of oral submucous fibrosis. Journal of dental sciences 2024 7 19 (3): 1834-1839. Chengbin Wei, Xuemin Shen, Wei Liu, Ruirui |
| Lynch syndrome in Mexican-Mestizo families: Genotype, phenotypes, and challenges in cascade testing among relatives at risk. Heliyon 2024 7 10 (11): e31855. Pamela Rivero-García, Yanin Chavarri-Guerra, José Luis Rodríguez Olivares, Jeffrey N Weitzel, Josef Herzog, Fernando Candanedo-González, Javier Ríos-Valencia, Osvaldo M Mutchinick, Jazmín Arteaga-Vázqu |
| Multi omics analysis of mitophagy subtypes and integration of machine learning for predicting immunotherapy responses in head and neck squamous cell carcinoma. Aging 2024 6 16 . Junzhi Liu, Huimin Li, Qiuping Dong, Zheng Lia |
| Precision Medicine to Redefine Insulin Secretion and Monogenic Diabetes-Randomized Controlled Trial (PRISM-RCT) in Chinese patients with young-onset diabetes: design, methods and baseline characteristics. BMJ open diabetes research & care 2024 6 12 (3): . Chun Kwan O, Ying Nan Fan, Baoqi Fan, Cadmon Lim, Eric S H Lau, Sandra T F Tsoi, Raymond Wan, Wai Yin Lai, Emily Wm Poon, Jane Ho, Cherry Cheuk Yee Ho, Chloe Fung, Eric Kp Lee, Samuel Ys Wong, Maggie Wang, Risa Ozaki, Elaine Cheung, Ronald Ching Wan Ma, Elaine Chow, Alice Pik Shan Kong, Andrea Luk, Juliana C N Ch |
| Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational psychiatry 2024 6 14 (1): 259. Jessica H Hall, Samuel J R A Chawner, , Jeanne Wolstencroft, David Skuse, Jeremy Hall, Peter Holmans, Michael J Owen, Marianne B M van den Br |
| Single-cell transcriptomics and Mendelian randomization reveal LUCAT1's role in right-sided colorectal cancer risk. Frontiers in genetics 2024 5 15 1357704. Zhihao Shang, Songyang Xi, Yueyang Lai, Haibo Che |
| Monocytic Differentiation of Human Acute Myeloid Leukemia Cells: A Proteomic and Phosphoproteomic Comparison of FAB-M4/M5 Patients with and without Nucleophosmin 1 Mutations. International journal of molecular sciences 2024 5 25 (10): . Frode Selheim, Elise Aasebø, Håkon Reikvam, Øystein Bruserud, Maria Hernandez-Valladar |
| Two remarkable serine/leucine polymorphisms in Helicobacter pylori: functional importance for serine protease HtrA and adhesin BabA. Cell communication and signaling : CCS 2024 5 22 (1): 250. Steffen Backert, Nicole Tegtmeyer, Anselm H C Horn, Heinrich Sticht, Bodo Li |
| The genetic landscape of autism spectrum disorder in the Middle Eastern population. Frontiers in genetics 2024 4 15 1363849. Yasser Al-Sarraj, Rowaida Z Taha, Eman Al-Dous, Dina Ahram, Somayyeh Abbasi, Eman Abuazab, Hibah Shaath, Wesal Habbab, Khaoula Errafii, Yosra Bejaoui, Maryam AlMotawa, Namat Khattab, Yasmin Abu Aqel, Karim E Shalaby, Amina Al-Ansari, Marios Kambouris, Adel Abouzohri, Iman Ghazal, Mohammed Tolfat, Fouad Alshaban, Hatem El-Shanti, Omar M E Albag |
| Updated analysis of the pharmacogenomics of pediatric bronchodilator response. Pharmacogenetics and genomics 2024 12 . Jennifer Brailsford, Guillaume Labilloy, Nolan Menze, Morgan Henson, Jennifer Fis |
| The potential role of CGRP in synuclein-associated neurodegenerative disorders. Frontiers in neuroscience 2024 11 18 1479830. Athanasia Alexoudi, Vincenzo Donadio, Elissaios Karageorgi |
| Maternal alcohol consumption during pregnancy and child development: Role of ADH1B and ALDH2 gene polymorphisms-The Yamanashi Adjunct Study of the Japan Environment and Children's Study. Alcohol, clinical & experimental research 2024 11 . Kunio Miyake, Sanae Otawa, Megumi Kushima, Hideki Yui, Ryoji Shinohara, Sayaka Horiuchi, Yuka Akiyama, Tadao Ooka, Reiji Kojima, Hiroshi Yokomichi, Zentaro Yamagata, |
| Clinicopathogenomic analysis of PI3K/AKT/PTEN-altered luminal metastatic breast cancer in Japan. Breast cancer (Tokyo, Japan) 2024 10 . Hiroshi Tada, Minoru Miyashita, Narumi Harada-Shoji, Akiko Ebata, Miku Sato, Tokiwa Motonari, Mika Yanagaki, Tomomi Kon, Aru Sakamoto, Takanori Ishi |
| Linked OXTR Variants Are Associated with Social Behavior Differences in Bonobos (Pan paniscus). bioRxiv : the preprint server for biology 2024 1 . Sara A Skiba, Alek Hansen, Ryan McCall, Azeeza Byers, Sarah Waldron, Amanda J Epping, Jared P Taglialatela, Martin L Huds |
| CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. Clinical genetics 2024 1 . Yu-Jie Chen, Wen-Jie Wang, Dong-Fang Zou, Jun-Xia Luo, Pei-Yan Jin, Liang Jin, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Yong-Jun Chen, |
| Replication of previous autism-GWAS hits suggests the association between NAA1, SORCS3, and GSDME and autism in the Han Chinese population. Heliyon 2024 1 10 (1): e23677. Fen Lin, Jun Li, Ziqi Wang, Tian Zhang, Tianlan Lu, Miaomiao Jiang, Kang Yang, Meixiang Jia, Dai Zhang, Lifang Wa |
| Genetic variants in DDX53 contribute to Autism Spectrum Disorder associated with the Xp22.11 locus. medRxiv : the preprint server for health sciences 2024 1 . Marcello Scala, Clarrisa A Bradley, Jennifer L Howe, Brett Trost, Nelson Bautista Salazar, Carole Shum, Miriam S Reuter, Jeffrey R MacDonald, Sangyoon Y Ko, Paul W Frankland, Leslie Granger, George Anadiotis, Verdiana Pullano, Alfredo Brusco, Roberto Keller, Sarah Parisotto, Helio F Pedro, Laina Lusk, Pamela Pojomovsky McDonnell, Ingo Helbig, Sureni V Mullegama, , Emilie D Douine, Bianca E Russell, Stanley F Nelson, Federico Zara, Stephen W Scher |
| Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman. International journal of molecular sciences 2025 1 25 (24): . Vijay Gupta, Afif Ben-Mahmoud, Ahmed B Idris, Jouke-Jan Hottenga, Wesal Habbab, Abeer Alsayegh, Hyung-Goo Kim, Watfa Al-Mamari, Lawrence W Stant |
| Investigating Sequence Variations in CNTNAP2 and SETBP1 Genes in Language Disorders. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology 2025 1 23 (1): 100-109. Betül Turan, Emine Gökta?, Necati Uzun, Ay?egül Tu?ba H?ra Selen, Ay?e Gül Zamani, Mahmut Selman Y?ld?r |
- Page last reviewed:Feb 1, 2024
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