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1دورية أكاديمية
المؤلفون: Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware
المصدر: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 18 (2023)
مصطلحات موضوعية: chromosomal microarray, congenital heart disease, conotruncal defects, genomics, neurodevelopment, Diseases of the circulatory (Cardiovascular) system, RC666-701
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2047-9980
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2دورية أكاديمية
المؤلفون: Tyler Shugg, Reynold C. Ly, Wilberforce Osei, Elizabeth J. Rowe, Caitlin A. Granfield, Ty C. Lynnes, Elizabeth B. Medeiros, Jennelle C. Hodge, Amy M. Breman, Bryan P. Schneider, S. Cenk Sahinalp, Ibrahim Numanagić, Benjamin A. Salisbury, Steven M. Bray, Ryan Ratcliff, Todd C. Skaar
المصدر: Frontiers in Oncology, Vol 13 (2023)
مصطلحات موضوعية: pharmacogenetic algorithm, next-generating sequencing, whole genome sequencing (WGS), whole exome sequencing (WES), pharmacogenomics (PGx), pharmacogenetics (PGx), Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
وصف الملف: electronic resource
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المؤلفون: Tatyana Milman, Hans E Grossniklaus, Gabrielle Goldman-Levy, Tero T Kivelä, Sarah E Coupland, Valerie A White, Hardeep Singh Mudhar, Charles G Eberhart, Robert M Verdijk, Steffen Heegaard, Anthony J Gill, Martine J Jager, Aberlardo A Rodriguez-Reyes, Bita Esmaeli, Jennelle C Hodge, Ian A Cree
المصدر: Ocular Oncology and Pathology.
مصطلحات موضوعية: General Nursing
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d851fd5d904af6a96bd31cf07218f294
https://doi.org/10.1159/000530730 -
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المصدر: Cytogenetic and Genome Research. 162:237-243
مصطلحات موضوعية: Genetics, Molecular Biology, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3c58bc1c4c5cbfe8cbbe75371332f2e1
https://doi.org/10.1159/000526660 -
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المؤلفون: Joseph D. Khoury, Eric Solary, Oussama Abla, Yassmine Akkari, Rita Alaggio, Jane F. Apperley, Rafael Bejar, Emilio Berti, Lambert Busque, John K. C. Chan, Weina Chen, Xueyan Chen, Wee-Joo Chng, John K. Choi, Isabel Colmenero, Sarah E. Coupland, Nicholas C. P. Cross, Daphne De Jong, M. Tarek Elghetany, Emiko Takahashi, Jean-Francois Emile, Judith Ferry, Linda Fogelstrand, Michaela Fontenay, Ulrich Germing, Sumeet Gujral, Torsten Haferlach, Claire Harrison, Jennelle C. Hodge, Shimin Hu, Joop H. Jansen, Rashmi Kanagal-Shamanna, Hagop M. Kantarjian, Christian P. Kratz, Xiao-Qiu Li, Megan S. Lim, Keith Loeb, Sanam Loghavi, Andrea Marcogliese, Soheil Meshinchi, Phillip Michaels, Kikkeri N. Naresh, Yasodha Natkunam, Reza Nejati, German Ott, Eric Padron, Keyur P. Patel, Nikhil Patkar, Jennifer Picarsic, Uwe Platzbecker, Irene Roberts, Anna Schuh, William Sewell, Reiner Siebert, Prashant Tembhare, Jeffrey Tyner, Srdan Verstovsek, Wei Wang, Brent Wood, Wenbin Xiao, Cecilia Yeung, Andreas Hochhaus
المساهمون: HAL UVSQ, Équipe, Département d'hématologie [Gustave Roussy], Institut Gustave Roussy (IGR), Service de pathologie [CHU Ambroise Paré], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Ambroise Paré [AP-HP], Université de Versailles Saint-Quentin-en-Yvelines - UFR Sciences de la santé Simone Veil (UVSQ Santé), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Institut Cochin (IC UM3 (UMR 8104 / U1016)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Open Access funding enabled and organized by Projekt DEAL.
المصدر: Leukemia, 36, 7, pp. 1703-1719
Leukemia
Leukemia, 2022, 36 (7), pp.1703-1719. ⟨10.1038/s41375-022-01613-1⟩
Leukemia, 36, 1703-1719
Khoury, J D, Solary, E, Abla, O, Akkari, Y, Alaggio, R, Apperley, J F, Bejar, R, Berti, E, Busque, L, Chan, J K C, Chen, W, Chen, X, Chng, W-J, Choi, J K, Colmenero, I, Coupland, S E, Cross, N C P, de Jong, D, Elghetany, M T, Takahashi, E, Emile, J-F, Ferry, J, Fogelstrand, L, Fontenay, M, Germing, U, Gujral, S, Haferlach, T, Harrison, C, Hodge, J C, Hu, S, Jansen, J H, Kanagal-Shamanna, R, Kantarjian, H M, Kratz, C P, Li, X-Q, Lim, M S, Loeb, K, Loghavi, S, Marcogliese, A, Meshinchi, S, Michaels, P, Naresh, K N, Natkunam, Y, Nejati, R, Ott, G, Padron, E, Patel, K P, Patkar, N, Picarsic, J, Platzbecker, U, Roberts, I, Schuh, A, Sewell, W, Siebert, R, Tembhare, P, Tyner, J, Verstovsek, S, Wang, W, Wood, B, Xiao, W, Yeung, C & Hochhaus, A 2022, ' The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours : Myeloid and Histiocytic/Dendritic Neoplasms ', Leukemia, vol. 36, no. 7, pp. 1703-1719 . https://doi.org/10.1038/s41375-022-01613-1مصطلحات موضوعية: [SDV.MHEP.HEM] Life Sciences [q-bio]/Human health and pathology/Hematology, Cancer Research, Haematological cancer, Cancer development and immune defence Radboud Institute for Molecular Life Sciences [Radboudumc 2], [SDV.CAN]Life Sciences [q-bio]/Cancer, [SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology, Hematology, World Health Organization, Oncology, [SDV.CAN] Life Sciences [q-bio]/Cancer, Hematologic Neoplasms, Diagnosis, Humans, Histiocytosis
وصف الملف: text; application/pdf
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المؤلفون: Andy Pao, Nan Deng, Jean Lopategui, Jennelle C Hodge, Snehal B Patel, Robert Bookstein, Christian Riley, Serhan Alkan, Angela Aguiluz, Zhenqui Liu, Navid Farahani, Myriam Chevarie-Davis
المصدر: Oncology and Therapy
مصطلحات موضوعية: Oncology, Tumor heterogeneity, medicine.medical_specialty, business.industry, Colorectal cancer, Cancer, medicine.disease, Somatic evolution in cancer, DNA sequencing, Metastasis, medicine.anatomical_structure, Therapy selection, Internal medicine, Cohort, Next-generation sequencing, Medicine, Paired primary and metastatic tumors, business, Lymph node, Patient-matched tumors, Selection (genetic algorithm), Original Research, Specimen selection
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المؤلفون: Amy M. Breman, Gail H. Vance, Priyanka Arya, Peggy Matlock, Jennelle C. Hodge
المصدر: Cytogenetic and Genome Research. 160:671-679
مصطلحات موضوعية: Genetics, Chromothripsis, Microarray analysis techniques, Breakpoint, Chromosomal rearrangement, Chromoplexy, Biology, Germline, Chromosome regions, Speech delay, medicine, medicine.symptom, Molecular Biology, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::1b806ea62ecb0776faf90454936fe975
https://doi.org/10.1159/000512898 -
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المؤلفون: Beth A. Pitel, Madina Sukhanova, Hui Chen, Xiaolin Hu, Deborah Ritter, Ashwini Yenamandra, Tracy Tucker, Francesc Sole, Jennelle C. Hodge, Shashirekha Shetty, Rashmi Kanagal-Shamanna, M. Anwar Iqbal, Rajyasree Emmadi, Gloria T. Haskell, Yajuan J. Liu, XinYan Lu, Karen Swisshelm, Patricia T. Greipp, Gordana Raca, Katherine B. Geiersbach, Xinjie Xu
المصدر: Cancer Genetics. :5-6
مصطلحات موضوعية: Cancer Research, Genetics, Molecular Biology
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المؤلفون: Bettina E. Mucha, Marianne Till, Tobias Linden, Mary Ann Thomas, Carl Ernst, Philippe M. Campeau, Jessica L. Waxler, Sau Wai Cheung, Damien Sanlaville, Jozef Gecz, Lesley M McGregor, Sanjay M. Sisodiya, Gary G. Chen, Michael Harbord, Mary Kay Koenig, Renee Perrier, Jennelle C. Hodge, Rhamat B. Adejumo, Jillian Nicholl, Norbert F. Ajeawung, Emmanuelle Lemyre, Brian G. Skotko, Siddharth Banka, Sirinart Molidperee, Renee Myriam Boucher
المصدر: Mucha, B E, Banka, S, Ajeawung, N F, Molidperee, S, Chen, G G, Koenig, M K, Adejumo, R B, Till, M, Harbord, M, Perrier, R, Lemyre, E, Boucher, R-M, Skotko, B G, Waxler, J L, Thomas, M A, Hodge, J C, Gecz, J, Nicholl, J, McGregor, L, Linden, T, Sisodiya, S M, Sanlaville, D, Cheung, S W, Ernst, C & Campeau, P M 2019, ' A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 21, no. 5, pp. 1058-1064 . https://doi.org/10.1038/s41436-018-0290-3
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Vacuolar Proton-Translocating ATPases, Pediatrics, medicine.medical_specialty, Microcephaly, Adolescent, Developmental Disabilities, MEDLINE, Nerve Tissue Proteins, 030105 genetics & heredity, 3-Phosphoinositide-Dependent Protein Kinases, Cohort Studies, Young Adult, 03 medical and health sciences, Epilepsy, Intellectual Disability, medicine, Humans, Child, Genetics (clinical), 16p13.3, business.industry, TBC1D24, Published Erratum, GTPase-Activating Proteins, Infant, Membrane Proteins, Syndrome, Microdeletion syndrome, medicine.disease, Spelling, 030104 developmental biology, Child, Preschool, Microdeletion, Female, Chromosome Deletion, business, Chromosomes, Human, Pair 16
وصف الملف: application/pdf
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المؤلفون: Xinjie Xu, Emma Huxley, Sally Jeffries, Amanda Dixon-McIver, Min Fang, Tracy Tucker, Gordana Raca, Patrick A. Lennon, M. Anwar Iqbal, Marilyn L. Slovak, Patricia T. Greipp, Jennelle C. Hodge, Rashmi Kanagal-Shamanna, Ashwini Yenamandra, Fabiola Quintero-Rivera, Christine R. Bryke, Shashi Shetty
المصدر: Cancer Genetics. :197-217
مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, medicine.medical_specialty, Myeloid, DNA Copy Number Variations, Loss of Heterozygosity, Genomics, Gene mutation, Biology, Loss of heterozygosity, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Genetics, medicine, Humans, Clinical significance, Molecular Biology, Myeloproliferative neoplasm, Myeloproliferative Disorders, business.industry, Cancer, medicine.disease, 030104 developmental biology, medicine.anatomical_structure, Myelodysplastic Syndromes, 030220 oncology & carcinogenesis, Personalized medicine, business
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