المؤلفون: Zhou Z; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Hughes K; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Saif N; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA.; Broad Institute of MIT and Harvard, Cambridge, MA, USA., Kim H; Department Kinesiology & Sport Management, Texas Tech University, Lubbock, TX, USA., Massett MP; Department Kinesiology & Sport Management, Texas Tech University, Lubbock, TX, USA., Zheng M; Department of Pediatrics, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Cecchi AC; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Guo D; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Murdock DR; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Pan P; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Clinton JS; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Wang J; Department of Pediatrics, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA., Greally JM; Department of Genetics, Albert Einstein College of Medicine, NY, USA., Milewicz DM; Division of Medical Genetics, Department of Internal Medicine, The University of Texas Health Science Center at Houston McGovern Medical School, Houston, TX, USA.

المصدر: BioRxiv : the preprint server for biology [bioRxiv] 2024 Aug 16. Date of Electronic Publication: 2024 Aug 16.

نوع المنشور: Journal Article; Preprint

بيانات الدورية: Country of Publication: United States NLM ID: 101680187 Publication Model: Electronic Cited Medium: Internet ISSN: 2692-8205 (Electronic) Linking ISSN: 26928205 NLM ISO Abbreviation: bioRxiv Subsets: PubMed not MEDLINE

المؤلفون: Garner M; University of Alabama at Birmingham., Rajani B; University of Texas Health Science Center at Houston., Vaidya P; University of Texas Health Science Center at Houston., Dayeh SA; University of Texas Health Science Center at Houston., Cecchi AC; University of Texas Health Science Center at Houston., Miyake CC; Baylor College of Medicine., Huff V; University of Texas MD Anderson Cancer Center., Wanat M; University of Houston College of Pharmacy., Wang E; University of Houston College of Pharmacy., Kurzlechner LM; Duke University School of Medicine., Landstrom AP; Duke University School of Medicine., An D; University of Texas Health Science Center at Houston., Liang Y; University of Texas Health Science Center at Houston., Moulik M; University of Pittsburgh School of Medicine., Wong TC; University of Pittsburgh School of Medicine., Cunha SR; University of Texas Health Science Center at Houston., Cannon A; University of Alabama at Birmingham., Holt RL; University of Alabama at Birmingham., Milewicz DM; University of Texas Health Science Center at Houston., Prakash SK; University of Texas Health Science Center at Houston.

المصدر: Research square [Res Sq] 2024 Jun 13. Date of Electronic Publication: 2024 Jun 13.

نوع المنشور: Journal Article; Preprint

بيانات الدورية: Country of Publication: United States NLM ID: 101768035 Publication Model: Electronic Cited Medium: Internet ISSN: 2693-5015 (Electronic) Linking ISSN: 26935015 NLM ISO Abbreviation: Res Sq Subsets: PubMed not MEDLINE

المؤلفون: Pinard A; Department of Internal Medicine, Division of Medical Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USA., Ye W; Howard Hughes Medical Institute, Department of Physiology, University of California San Francisco, San Francisco, CA 94158, USA., Fraser SM; Department of Pediatrics, Division of Child Neurology, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USA., Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA., Pichurin P; Department of Clinical Genomics, Mayo Clinic, Rochester, MN 55902, USA., Hickey SE; Department of Pediatrics, The Ohio State University, Columbus, OH 43210, USA.; Division of Genetic and Genomic Medicine, Nationwide Children's Hospital, Columbus, OH 43205, USA., Guo D; Department of Internal Medicine, Division of Medical Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USA., Cecchi AC; Department of Internal Medicine, Division of Medical Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USA., Boerio ML; Department of Internal Medicine, Division of Medical Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USA., Guey S; Université de Paris, Inserm U1141, AP-HP Groupe hospitalier Lariboisière Saint Louis, 75019 Paris, France., Aloui C; Université de Paris, Inserm U1141, AP-HP Groupe hospitalier Lariboisière Saint Louis, 75019 Paris, France., Lee K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA., Kraemer M; Department of Neurology, Alfried Krupp-Hospital, 45131 Essen, Germany.; Department of Neurology, Medical Faculty, Heinrich-Heine-University, 40225 Düsseldorf, Germany., Alyemni SO; UCL School of Pharmacy, Bloomsbury, London WC1N 1AX, UK., Bamshad MJ; Division of Genetics Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA., Nickerson DA; Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA., Tournier-Lasserve E; Université de Paris, Inserm U1141, AP-HP Groupe hospitalier Lariboisière Saint Louis, 75019 Paris, France.; AP-HP, Service de génétique moléculaire neurovasculaire, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'oeil, Groupe Hospitalier Saint-Louis Lariboisière, 75010 Paris, France., Haider S; UCL School of Pharmacy, Bloomsbury, London WC1N 1AX, UK.; UCL Centre for Advanced Research Computing, University College London, London WC1H 9RN, UK., Jin SC; Department of Genetics, Washington University School of Medicine, St Louis, MO 63110, USA.; Department of Pediatrics, Washington University School of Medicine, St Louis, MO 63110, USA., Smith ER; Department of Neurosurgery, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA., Kahle KT; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT 06510, USA.; Department of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.; Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA., Jan LY; Howard Hughes Medical Institute, Department of Physiology, University of California San Francisco, San Francisco, CA 94158, USA., He M; Howard Hughes Medical Institute, Department of Physiology, University of California San Francisco, San Francisco, CA 94158, USA.; School of Biomedical Sciences, The University of Hong Kong, Pok Fu Lam, Hong Kong SAR, China., Milewicz DM; Department of Internal Medicine, Division of Medical Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

مؤلفون مشاركون: University of Washington Center for Mendelian Genomics

المصدر: Brain : a journal of neurology [Brain] 2023 Sep 01; Vol. 146 (9), pp. 3616-3623.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

مواضيع طبية MeSH: Anoctamin-1*/genetics , Moyamoya Disease*/genetics, Child ; Humans ; Young Adult ; Chloride Channels/genetics ; Neoplasm Proteins/genetics

SCR Disease Name: Moyamoya disease 1

المؤلفون: Guo DC; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Duan X; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Mimnagh K; Department of Internal Medicine, WVU School of Medicine-Charleston Division (Retired), Morgantown, West Virginia, USA., Cecchi AC; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Marin IC; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Yu Y; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Velasco WV; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Lee K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Zhu X; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Murdock DR; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA., Leal SM; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA., Wheeler MM; Genome Sciences, University of Washington, Seattle, Washington, USA., Smith J; Genome Sciences, University of Washington, Seattle, Washington, USA., Bamshad MJ; Genome Sciences, University of Washington, Seattle, Washington, USA., Milewicz DM; Department of Internal Medicine, University of Texas Health Science Center at Houston (UTHealth), Houston, Texas, USA.

المصدر: Clinical genetics [Clin Genet] 2023 Jun; Vol. 103 (6), pp. 704-708. Date of Electronic Publication: 2023 Mar 07.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

مواضيع طبية MeSH: Marfan Syndrome*/genetics , Aortic Diseases*, Humans ; Fibrillin-1/genetics ; Mutation ; Phenotype

المؤلفون: Zhou Z; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, 6431 Fannin Street, MSB 6.100, Houston, TX 77030, USA., Cecchi AC; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, 6431 Fannin Street, MSB 6.100, Houston, TX 77030, USA., Prakash SK; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, 6431 Fannin Street, MSB 6.100, Houston, TX 77030, USA., Milewicz DM; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, 6431 Fannin Street, MSB 6.100, Houston, TX 77030, USA.

المصدر: Genes [Genes (Basel)] 2022 Oct 07; Vol. 13 (10). Date of Electronic Publication: 2022 Oct 07.

نوع المنشور: Journal Article; Review; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

مواضيع طبية MeSH: Aortic Aneurysm, Thoracic*/epidemiology , Aortic Aneurysm, Thoracic*/genetics , Aortic Dissection*/epidemiology , Aortic Dissection*/genetics, Humans ; Aorta ; Risk Factors

المؤلفون: Cecchi AC; Division of Medical Genetics Department of Internal Medicine University of Texas Health Science Center at Houston TX., Boerio ML; Division of Medical Genetics Department of Internal Medicine University of Texas Health Science Center at Houston TX., Marin I; Division of Medical Genetics Department of Internal Medicine University of Texas Health Science Center at Houston TX., Pinard A; Division of Medical Genetics Department of Internal Medicine University of Texas Health Science Center at Houston TX., Milewicz DM; Division of Medical Genetics Department of Internal Medicine University of Texas Health Science Center at Houston TX.

المصدر: Journal of the American Heart Association [J Am Heart Assoc] 2022 Apr 19; Vol. 11 (8), pp. e025441. Date of Electronic Publication: 2022 Apr 06.

نوع المنشور: Editorial; Comment

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101580524 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2047-9980 (Electronic) Linking ISSN: 20479980 NLM ISO Abbreviation: J Am Heart Assoc Subsets: MEDLINE

مواضيع طبية MeSH: Aortic Dissection*/diagnosis , Aortic Dissection*/genetics , Aortic Dissection*/prevention & control , Aortic Aneurysm, Thoracic*/diagnosis, Humans ; Pedigree ; Risk Assessment

المؤلفون: Cecchi AC; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center, Houston, TX. Electronic address: Alana.C.Cecchi@uth.tmc.edu., Drake M; McGovern Medical School, University of Texas Health Science Center, Houston, TX., Campos C; Genetic Aortic Disorders Association Canada, Mississauga, Ontario, Canada., Howitt J; Aortic Dissection Collaborative Advisory Group, Seattle, WA., Medina J; Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA., Damrauer SM; Department of Surgery and the Cardiovascular Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Department of Surgery, Corporal Michael Crescenz Veterans Affairs Medical Center, Philadelphia, PA., Shalhub S; Division of Vascular Surgery, Department of Surgery, University of Washington School of Medicine, Seattle, WA., Milewicz DM; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center, Houston, TX.

مؤلفون مشاركون: Aortic Dissection Collaborative

المصدر: Seminars in vascular surgery [Semin Vasc Surg] 2022 Mar; Vol. 35 (1), pp. 51-59. Date of Electronic Publication: 2022 Feb 25.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: W.B. Saunders Country of Publication: United States NLM ID: 8809602 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1558-4518 (Electronic) Linking ISSN: 08957967 NLM ISO Abbreviation: Semin Vasc Surg Subsets: MEDLINE

مواضيع طبية MeSH: Aortic Dissection*/diagnostic imaging , Aortic Dissection*/genetics , Aortic Dissection*/prevention & control , Genomic Medicine*, Humans ; Quality of Life ; Risk Assessment ; Risk Factors

المؤلفون: Cecchi AC; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Texas, USA., Haidar A; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Texas, USA., Marin I; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Texas, USA., Kwartler CS; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Texas, USA., Prakash SK; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Texas, USA., Milewicz DM; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Texas, USA.

المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2022 Feb; Vol. 188 (2), pp. 628-634. Date of Electronic Publication: 2021 Oct 13.

نوع المنشور: Case Reports; Research Support, N.I.H., Extramural

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

مواضيع طبية MeSH: Aortic Diseases*/complications , Aortic Diseases*/diagnosis , Aortic Diseases*/genetics , Cardiomyopathy, Dilated*/complications , Cardiomyopathy, Dilated*/diagnosis , Cardiomyopathy, Dilated*/genetics , Intellectual Disability*/genetics , Marfan Syndrome*/complications , Marfan Syndrome*/diagnosis , Marfan Syndrome*/genetics, Adult ; DNA (Cytosine-5-)-Methyltransferases/genetics ; DNA Methyltransferase 3A ; Dilatation ; Humans ; Mutation

المؤلفون: Rommens KL; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Sandhu HK; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Miller CC 3rd; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Cecchi AC; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Prakash SK; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex; Division of Cardiology, Department of Internal Medicine, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Saqib NU; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Charlton-Ouw KM; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Milewicz DM; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Estrera AL; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Safi HJ; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex., Afifi RO; Department of Cardiothoracic and Vascular Surgery, McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth), Houston, Tex. Electronic address: Rana.O.Afifi@uth.tmc.edu.

المصدر: Journal of vascular surgery [J Vasc Surg] 2021 Oct; Vol. 74 (4), pp. 1135-1142.e1. Date of Electronic Publication: 2021 Apr 20.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: United States NLM ID: 8407742 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-6809 (Electronic) Linking ISSN: 07415214 NLM ISO Abbreviation: J Vasc Surg Subsets: MEDLINE

مواضيع طبية MeSH: Hospitalization* , Maternal Age* , Reproductive Health*, Aortic Dissection/*epidemiology , Aortic Aneurysm/*epidemiology , Pregnancy Complications, Cardiovascular/*epidemiology, Adult ; Aortic Dissection/diagnostic imaging ; Aortic Dissection/mortality ; Aortic Dissection/therapy ; Aortic Aneurysm/diagnostic imaging ; Aortic Aneurysm/mortality ; Aortic Aneurysm/therapy ; Databases, Factual ; Female ; Hospital Mortality ; Humans ; Maternal Mortality ; Middle Aged ; Pregnancy ; Pregnancy Complications, Cardiovascular/diagnostic imaging ; Pregnancy Complications, Cardiovascular/mortality ; Pregnancy Complications, Cardiovascular/therapy ; Prognosis ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Texas/epidemiology ; Time Factors

المؤلفون: Milewicz DM; McGovern Medical School, Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center, Houston, TX, USA - dianna.m.milewicz@uth.tmc.edu., Guo D; McGovern Medical School, Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center, Houston, TX, USA., Hostetler E; McGovern Medical School, Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center, Houston, TX, USA., Marin I; McGovern Medical School, Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center, Houston, TX, USA., Pinard AC; McGovern Medical School, Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center, Houston, TX, USA., Cecchi AC; McGovern Medical School, Division of Medical Genetics, Department of Internal Medicine, University of Texas Health Science Center, Houston, TX, USA.

المصدر: The Journal of cardiovascular surgery [J Cardiovasc Surg (Torino)] 2021 Jun; Vol. 62 (3), pp. 203-210. Date of Electronic Publication: 2021 Mar 18.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Edizioni Minerva Medica Country of Publication: Italy NLM ID: 0066127 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1827-191X (Electronic) Linking ISSN: 00219509 NLM ISO Abbreviation: J Cardiovasc Surg (Torino) Subsets: MEDLINE

مواضيع طبية MeSH: Genetic Predisposition to Disease*, Aortic Dissection/*genetics , Aortic Aneurysm, Thoracic/*genetics, Acute Disease ; Humans ; Risk Factors