An Empirical Assessment of Security and Privacy Risks of Web-Based Chatbots

Autor: Waheed, N, Ikram, M, Hashmi, SS, He, X, Nanda, P

Web-based chatbots provide website owners with the benefits of increased sales, immediate response to their customers, and insight into customer behaviour. While Web-based chatbots are getting popular, they have not received much scrutiny from securi

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https://hdl.handle.net/10453/166252

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Medical students' self-perceived knowledge and clinical comfort with genetics in Pakistan.

Autor: Arshad M; Wayne State University School of Medicine, Center for Molecular Medicine and Genetics, Detroit, Michigan, USA.; Henry Ford Health System, Detroit, Michigan, USA., Trepanier A; Wayne State University School of Medicine, Center for Molecular Medicine and Genetics, Detroit, Michigan, USA., Hashmi SS; Department of Pediatrics, McGovern Medical School at the University of Texas Health Science Center at Houston and Children's Memorial Hermann Hospital, Houston, Texas, USA., Naeem R; Albert Einstein College of Medicine, New York City, New York, USA., Mehmood S; University of Health Sciences, Lahore, Punjab, Pakistan., Ashfaq M; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston and Children's Memorial Hermann Hospital, Houston, Texas, USA.

Publikováno v: Journal of genetic counseling [J Genet Couns] 2024 Oct; Vol. 33 (5), pp. 1113-1125. Date of Electronic Publication: 2023 Nov 13.

Well-Child Visits for Early Detection and Management of Maternal Postpartum Hypertensive Disorders.

Autor: Amro FH; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston., Smith KC; Division of Community & General Pediatrics, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston., Hashmi SS; Division of Community & General Pediatrics, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston., Barratt MS; Division of Community & General Pediatrics, Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston., Carlson R; Department of Obstetrics, Gynecology, and Reproductive Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston., Sankey KM; Department of Obstetrics, Gynecology, and Reproductive Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston., Bartal MF; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston., Blackwell SC; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston., Chauhan SP; Department of Maternal-Fetal Medicine, Delaware Center of Maternal-Fetal Medicine, Newark, Deleware., Sibai BM; Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston.

Publikováno v: JAMA network open [JAMA Netw Open] 2024 Jun 03; Vol. 7 (6), pp. e2416844. Date of Electronic Publication: 2024 Jun 03.

Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension.

Autor: Copeland I; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Wonkam-Tingang E; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA., Gupta-Malhotra M; Department of Cardiology, Baylor College of Medicine, San Antonio, Texas, USA., Hashmi SS; Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas, USA., Han Y; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA., Jajoo A; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA., Hall NJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; US Department of Agriculture Agricultural Research Service Children's Nutrition Research Center, Baylor College of Medicine, Houston, Texas, USA., Hernandez PP; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; US Department of Agriculture Agricultural Research Service Children's Nutrition Research Center, Baylor College of Medicine, Houston, Texas, USA., Lie N; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA.; US Department of Agriculture Agricultural Research Service Children's Nutrition Research Center, Baylor College of Medicine, Houston, Texas, USA., Liu D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Xu J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Rosenfeld J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Baylor Genetics, Houston, Texas, USA., Haldipur A; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA., Desire Z; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA., Coban-Akdemir ZH; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Human Genetics Center, The University of Texas Health Science Center at Houston, Houston, Texas, USA., Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Department of Molecular Physiology and Biophysics., Li Q; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA., Chao HT; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Division of Neurology and Developmental Neuroscience, Department of Pediatrics; and.; Department of Neuroscience, Baylor College of Medicine, Houston, Texas, USA.; Cain Pediatric Neurology Research Foundation Laboratories, Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital and Baylor College of Medicine, Houston, Texas, USA.; McNair Medical Institute, The Robert and Janice McNair Foundation, Houston, Texas, USA., Zaske AM; Department of Pediatrics, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas, USA., Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA., Milewicz DM; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas, USA., Shete S; The University of Texas MD Anderson Cancer Center, Houston, Texas, USA., Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; McNair Medical Institute, The Robert and Janice McNair Foundation, Houston, Texas, USA., Hanchard NA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Childhood Complex Disease Genomics Section, National Human Genome Research Institute, NIH, Bethesda, USA.

Publikováno v: JCI insight [JCI Insight] 2024 May 08; Vol. 9 (9). Date of Electronic Publication: 2024 May 08.