المؤلفون: Vashishtha, Sameer, Singh, Prashant Kumar, Rizvi, Mohd., Garg, Paras

المصدر: 2024 IEEE International Symposium on Circuits and Systems (ISCAS) Circuits and Systems (ISCAS), 2024 IEEE International Symposium on. :1-5 May, 2024

Relation: 2024 IEEE International Symposium on Circuits and Systems (ISCAS)

المؤلفون: Sharma, Anamika, Pandey, Luv, Garg, Paras, Zele, Rajesh

المصدر: 2024 IEEE International Symposium on Circuits and Systems (ISCAS) Circuits and Systems (ISCAS), 2024 IEEE International Symposium on. :1-5 May, 2024

Relation: 2024 IEEE International Symposium on Circuits and Systems (ISCAS)

المؤلفون: Vashishtha, Sameer, Rizvi, Saiyid Mohammad Irshad, Garg, Paras

المصدر: 2023 IEEE 27th Workshop on Signal and Power Integrity (SPI) Signal and Power Integrity (SPI), 2023 IEEE 27th Workshop on. :1-3 May, 2023

Relation: 2023 IEEE 27th Workshop on Signal and Power Integrity (SPI)

المؤلفون: Ramtiyal, Bharti, Garg, Paras, Johari, Shubha, Rathore, Ajay Pal Singh, Thakrey, Abhilash

المصدر: Journal of Global Operations and Strategic Sourcing, 2023, Vol. 17, Issue 1, pp. 1-27.

URL الوصول: http://www.emeraldinsight.com/doi/10.1108/JGOSS-03-2023-0014

المؤلفون: Garg, Paras, Jadhav, Bharati, Rodriguez, Oscar L, Patel, Nihir, Martin-Trujillo, Alejandro, Jain, Miten, Metsu, Sofie, Olsen, Hugh, Paten, Benedict, Ritz, Beate, Kooy, R Frank, Gecz, Jozef, Sharp, Andrew J

المصدر: American Journal of Human Genetics. 107(4)

مصطلحات موضوعية: Brain Disorders, Rare Diseases, Genetics, Human Genome, 2.1 Biological and endogenous factors, Aetiology, BRCA1 Protein, DNA Methylation, Epigenesis, Genetic, Female, Folic Acid, Gene Silencing, Genetic Diseases, Inborn, Genetic Loci, Genetic Variation, Genome, Human, High-Throughput Nucleotide Sequencing, Humans, Male, Promoter Regions, Genetic, Receptors, LDL, Trinucleotide Repeat Expansion, Twins, Monozygotic, DNA methylation, epimutation, epivariation, folate-sensitive fragile site, repeat expansion, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/8ws7j356

المؤلفون: Breen, Michael S, Garg, Paras, Tang, Lara, Mendonca, Danielle, Levy, Tess, Barbosa, Mafalda, Arnett, Anne B, Kurtz-Nelson, Evangeline, Agolini, Emanuele, Battaglia, Agatino, Chiocchetti, Andreas G, Freitag, Christine M, Garcia-Alcon, Alicia, Grammatico, Paola, Hertz-Picciotto, Irva, Ludena-Rodriguez, Yunin, Moreno, Carmen, Novelli, Antonio, Parellada, Mara, Pascolini, Giulia, Tassone, Flora, Grice, Dorothy E, Di Marino, Daniele, Bernier, Raphael A, Kolevzon, Alexander, Sharp, Andrew J, Buxbaum, Joseph D, Siper, Paige M, De Rubeis, Silvia

المصدر: American Journal of Human Genetics. 107(3)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Human Genome, Brain Disorders, Basic Behavioral and Social Science, Intellectual and Developmental Disabilities (IDD), Mental Health, Behavioral and Social Science, Autism, Neurosciences, Clinical Research, Aetiology, 2.1 Biological and endogenous factors, Neurological, Autism Spectrum Disorder, Child, DNA Methylation, Developmental Disabilities, Epigenesis, Genetic, Female, Homeodomain Proteins, Humans, Intellectual Disability, Male, Mutation, Nerve Tissue Proteins, Neurodevelopmental Disorders, Phenotype, Transcriptome, ADNP, DNA methylation, Helsmoortel-Van der Aa syndrome, autism spectrum disorder, biomarkers, epigenetic signature, episignature, genotype-phenotype correlations, intellectual disability, neurodevelopmental disorders, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6397x8vm

المؤلفون: Garg, Paras, Jadhav, Bharati, Lee, William, Rodriguez, Oscar L., Martin-Trujillo, Alejandro, Sharp, Andrew J.

المصدر: In The American Journal of Human Genetics 2 June 2022 109(6):1065-1076

المؤلفون: Betschart, Raphael O., Koliopanos, Georgios, Garg, Paras, Guo, Linlin, Rossi, Massimiliano, Schönherr, Sebastian, Blankenberg, Stefan, Twerenbold, Raphael, Zeller, Tanja, Ziegler, Andreas

المصدر: BioMed; Jun2024, Vol. 4 Issue 2, p156-170, 15p

مصطلحات موضوعية: GENETIC variation, LIPOPROTEINS, DNA copy number variations, DNA sequencing, SHORT tandem repeat analysis

المؤلفون: Jadhav, Bharati, Garg, Paras, van Vugt, Joke J. F. A., Garikano, Kristina Ibanez, Gagliardi, Delia, Lee, William, Martin-Trujillo, Alejandro, Gies, Scott L., Barbosa, Mafalda, Jain, Miten, Houlden, Henry, Paten, Benedict, Veldink, Jan, Tucci, Arianna, Sharp, Andrew J.

المصدر: medRxiv

مصطلحات موضوعية: Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmc_________::e02c3ef89e9750c72d1cf5d7503a6d18
https://europepmc.org/articles/PMC10187445/

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