Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 413 Records) |
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Integrative analysis of cuproptosis-associated genes for predicting immunotherapy response in single-cell and multi-cohort studies. The journal of gene medicine 2023 9 e3600. Hua Li, Yichen Wang, Guangxiao Li, Jian Xiong, Lingshan Qin, Qirong Wen, Chaomin Y |
Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism. American journal of medical genetics. Part A 2023 9 . Dale Cameron Wright, Maria Lourdes Baluyot, Johanna Carmichael, Artur Darmanian, Ngaire Jose, Con Ngo, Luke St Heaps, Amber Yendle, Katherine Holman, Sylvia Ziso, Feroza Khan, Anne Masi, Natalie Silove, Valsa Eap |
Cognitive-Behavioral Profile in Pediatric Patients with Syndrome 5p-; Genotype-Phenotype Correlationships. Genes 2023 8 14 (8): . Cristina Bel-Fenellós, Chantal Biencinto-López, Belén Sáenz-Rico, Adolfo Hernández, Ana Karen Sandoval-Talamantes, Jair Tenorio-Castaño, Pablo Lapunzina, Julián Neva |
SLC22A3 rs2048327 Polymorphism Is Associated with Diabetic Retinopathy in Caucasians with Type 2 Diabetes Mellitus. Biomedicines 2023 8 11 (8): . Emin Grbi?, Mojca Globo?nik Petrovi?, Ines Cilenšek, Danijel Petrov |
Wildtype peers rescue social play and 50-kHz ultrasonic vocalization deficits in juvenile female Cacna1c heterozygous rats. Frontiers in behavioral neuroscience 2023 8 17 1190272. Rebecca Bogdan, Rukhshona Kayumova, Rainer K W Schwarting, Markus Wöhr, Theresa M Kis |
Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder. Gene 2023 8 147723. Yulian Fang, Yaqiong Cui, Zhaoqing Yin, Mengzhu Hou, Pan Guo, Hanjie Wang, Nan Liu, Chunquan Cai, Mingbang Wa |
A pilot study on glutamate receptor and carrier gene variants and risk of childhood autism spectrum. Metabolic brain disease 2023 8 . Jun Liu, Jing Yan, Fei Qu, Weiming Mo, Hong Yu, Pingfang Hu, Zengyu Zha |
The genetics of autism spectrum disorder in an East African familial cohort. Cell genomics 2023 7 3 (7): 100322. Islam Oguz Tuncay, Darlene DeVries, Ashlesha Gogate, Kiran Kaur, Ashwani Kumar, Chao Xing, Kimberly Goodspeed, Leah Seyoum-Tesfa, Maria H Chahro |
Genes associated with spontaneous brain activity changes in clinically different patients with major depressive disorder: A transcription-neuroimaging association study. CNS neuroscience & therapeutics 2023 6 . Wenshuang Zhu, Feng Liu, Jilian Fu, Wen Qin, Kaizhong Xue, Jie Tang, Yong Zhang, Chunshui |
Establishment and validation of a clinical severity scoring system for succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 2023 5 . Itay Tokatly Latzer, Jean-Baptiste Roullet, K Michael Gibson, Phillip L Pea |
How Subjective and Objective Factors in Research and Practice May Perpetuate Health Disparities amongst Patients with Traumatic Brain Injury. American journal of physical medicine & rehabilitation 2023 5 . Karen T Johnson, HyunBin You, Melissa Kandel, Tolu O Oyesan |
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 |
eQTL colocalization analysis highlights novel susceptibility genes in Autism Spectrum Disorders (ASD). Translational psychiatry 2023 11 13 (1): 336. S Dominguez-Alonso, A Carracedo, C Rodriguez-Fonten |
Spatial transcriptomics suggests that alterations occur in the preneoplastic breast microenvironment of BRCA1/2 mutation carriers. Molecular cancer research : MCR 2023 10 . Anthony Caputo, Kavya Vipparthi, Peter Bazeley, Erinn Downs-Kelly, Patrick McIntire, Lauren A Duckworth, Ying Ni, Bo Hu, Ruth A Keri, Mihriban Karaayv |
Somatosensory pathway dysfunction in patients with amyotrophic lateral sclerosis in a completely locked-in state. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology 2023 10 . Toshio Shimizu, Yuki Nakayama, Kentaro Hayashi, Yoko Mochizuki, Chiharu Matsuda, Michiko Haraguchi, Kota Bokuda, Takashi Komori, Kazushi Takahas |
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 |
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 |
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 |
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