المؤلفون: Alexander S. F. Berry, Brenda M. Finucane, Scott M. Myers, Lauren K. Walsh, John M. Seibert, Christa Lese Martin, David H. Ledbetter, Matthew T. Oetjens

المصدر: Nature Communications, Vol 15, Iss 1, Pp 1-11 (2024)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2041-1723

URL الوصول: https://doaj.org/article/f0da2cc7458a4d61b2c706f50ed3eb7e

المؤلفون: Samuel S. Gidding, H. Lester Kirchner, Andrew Brangan, William Howard, Melissa A. Kelly, Kelly D. Myers, Kelly M. Morgan, Matthew T. Oetjens, Timothy C. Shuey, David Staszak, Natasha T. Strande, Nicole L. Walters, Kristen D. Yu, Katherine A. Wilemon, Marc S. Williams, Amy C. Sturm, Laney K. Jones

المصدر: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 13 (2023)

مصطلحات موضوعية: electronic health records, familial hypercholesterolemia, genetic testing, machine learning, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2047-9980

URL الوصول: https://doaj.org/article/05b8f792bfdd43bc923992cd079ffc47

المؤلفون: Yifan Wang, Taejeong Bae, Jeremy Thorpe, Maxwell A. Sherman, Attila G. Jones, Sean Cho, Kenneth Daily, Yanmei Dou, Javier Ganz, Alon Galor, Irene Lobon, Reenal Pattni, Chaggai Rosenbluh, Simone Tomasi, Livia Tomasini, Xiaoxu Yang, Bo Zhou, Schahram Akbarian, Laurel L. Ball, Sara Bizzotto, Sarah B. Emery, Ryan Doan, Liana Fasching, Yeongjun Jang, David Juan, Esther Lizano, Lovelace J. Luquette, John B. Moldovan, Rujuta Narurkar, Matthew T. Oetjens, Rachel E. Rodin, Shobana Sekar, Joo Heon Shin, Eduardo Soriano, Richard E. Straub, Weichen Zhou, Andrew Chess, Joseph G. Gleeson, Tomas Marquès-Bonet, Peter J. Park, Mette A. Peters, Jonathan Pevsner, Christopher A. Walsh, Daniel R. Weinberger, Brain Somatic Mosaicism Network, Flora M. Vaccarino, John V. Moran, Alexander E. Urban, Jeffrey M. Kidd, Ryan E. Mills, Alexej Abyzov

المصدر: Genome Biology, Vol 22, Iss 1, Pp 1-32 (2021)

مصطلحات موضوعية: Biology (General), QH301-705.5, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1474-760X

URL الوصول: https://doaj.org/article/ed8ec2a7cb594e94ba5848bb9fd9be5a

المؤلفون: Matthew T. Oetjens, Axel Martin, Krishna R. Veeramah, Jeffrey M. Kidd

المصدر: BMC Genomics, Vol 19, Iss 1, Pp 1-9 (2018)

مصطلحات موضوعية: Canid, Y-chromosome haplogroups, Ancient dog, Biotechnology, TP248.13-248.65, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12864-018-4749-z; https://doaj.org/toc/1471-2164

URL الوصول: https://doaj.org/article/eed8fa23fb3f40af8c12c68fbfc4f735

المؤلفون: Matthew T. Oetjens, Kristin eBrown-Gentry, Robert eGoodloe, Holli H. Dilks, Dana C. Crawford

المصدر: Frontiers in Genetics, Vol 7 (2016)

مصطلحات موضوعية: Epidemiology, genetic epidemiology, population stratification, NHANES, Cross-sectional, EAGLE, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://journal.frontiersin.org/Journal/10.3389/fgene.2016.00076/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/260e8c20680c42f69f82397ac0511e2a

المؤلفون: Yifan Wang (380120), Taejeong Bae (9637278), Jeremy Thorpe (10494889), Maxwell A. Sherman (10494892), Attila G. Jones (10494895), Sean Cho (842114), Kenneth Daily (150164), Yanmei Dou (10494898), Javier Ganz (580190), Alon Galor (10494901), Irene Lobon (10494904), Reenal Pattni (10494907), Chaggai Rosenbluh (10494910), Simone Tomasi (139458), Livia Tomasini (10494913), Xiaoxu Yang (673521), Bo Zhou (15092), Schahram Akbarian (117762), Laurel L. Ball (10494916), Sara Bizzotto (10138543), Sarah B. Emery (3244203), Ryan Doan (572108), Liana Fasching (10494919), Yeongjun Jang (146006), David Juan (19252), Esther Lizano (5986972), Lovelace J. Luquette (10494922), John B. Moldovan (10494925), Rujuta Narurkar (10494928), Matthew T. Oetjens (9635214), Rachel E. Rodin (10138540), Shobana Sekar (4243036), Joo Heon Shin (7432022), Eduardo Soriano (196519), Richard E. Straub (10494931), Weichen Zhou (6004454), Andrew Chess (63935), Joseph G. Gleeson (10494934), Tomas Marquès-Bonet (10494937), Peter J. Park (8186340), Mette A. Peters (6641051), Jonathan Pevsner (15767), Christopher A. Walsh (8667276), Daniel R. Weinberger (9283256), Flora M. Vaccarino (10494940), John V. Moran (10494943), Alexander E. Urban (10494946), Jeffrey M. Kidd (7465493), Ryan E. Mills (10494949), Alexej Abyzov (9637287)

مصطلحات موضوعية: Genetics, mosaic SNVs, Brain Somatic Mosaicism Network, nucleotide variants, DNA repair, single-nucleotide variants, bulk DNA samples, brain regions, mosaic variants, Somatic mosaicism, non-cancerous tissues, brain tissue Abstract Background Po., variant allele fractions, Comprehensive identification, dural fibroblasts, dura mater, multi-institutional study, DNA replication, cell lineage trees, dorsolateral prefrontal cortex, whole-genome sequencing data

Relation: https://figshare.com/articles/journal_contribution/Additional_file_5_of_Comprehensive_identification_of_somatic_nucleotide_variants_in_human_brain_tissue/14337778

الاتاحة: https://doi.org/10.6084/m9.figshare.14337778.v1

المؤلفون: Yifan Wang (380120), Taejeong Bae (9637278), Jeremy Thorpe (10494889), Maxwell A. Sherman (10494892), Attila G. Jones (10494895), Sean Cho (842114), Kenneth Daily (150164), Yanmei Dou (10494898), Javier Ganz (580190), Alon Galor (10494901), Irene Lobon (10494904), Reenal Pattni (10494907), Chaggai Rosenbluh (10494910), Simone Tomasi (139458), Livia Tomasini (10494913), Xiaoxu Yang (673521), Bo Zhou (15092), Schahram Akbarian (117762), Laurel L. Ball (10494916), Sara Bizzotto (10138543), Sarah B. Emery (3244203), Ryan Doan (572108), Liana Fasching (10494919), Yeongjun Jang (146006), David Juan (19252), Esther Lizano (5986972), Lovelace J. Luquette (10494922), John B. Moldovan (10494925), Rujuta Narurkar (10494928), Matthew T. Oetjens (9635214), Rachel E. Rodin (10138540), Shobana Sekar (4243036), Joo Heon Shin (7432022), Eduardo Soriano (196519), Richard E. Straub (10494931), Weichen Zhou (6004454), Andrew Chess (63935), Joseph G. Gleeson (10494934), Tomas Marquès-Bonet (10494937), Peter J. Park (8186340), Mette A. Peters (6641051), Jonathan Pevsner (15767), Christopher A. Walsh (8667276), Daniel R. Weinberger (9283256), Flora M. Vaccarino (10494940), John V. Moran (10494943), Alexander E. Urban (10494946), Jeffrey M. Kidd (7465493), Ryan E. Mills (10494949), Alexej Abyzov (9637287)

مصطلحات موضوعية: Genetics, mosaic SNVs, Brain Somatic Mosaicism Network, nucleotide variants, DNA repair, single-nucleotide variants, bulk DNA samples, brain regions, mosaic variants, Somatic mosaicism, non-cancerous tissues, brain tissue Abstract Background Po., variant allele fractions, Comprehensive identification, dural fibroblasts, dura mater, multi-institutional study, DNA replication, cell lineage trees, dorsolateral prefrontal cortex, whole-genome sequencing data

Relation: https://figshare.com/articles/journal_contribution/Additional_file_1_of_Comprehensive_identification_of_somatic_nucleotide_variants_in_human_brain_tissue/14337760

الاتاحة: https://doi.org/10.6084/m9.figshare.14337760.v1

المؤلفون: Yifan Wang (380120), Taejeong Bae (9637278), Jeremy Thorpe (10494889), Maxwell A. Sherman (10494892), Attila G. Jones (10494895), Sean Cho (842114), Kenneth Daily (150164), Yanmei Dou (10494898), Javier Ganz (580190), Alon Galor (10494901), Irene Lobon (10494904), Reenal Pattni (10494907), Chaggai Rosenbluh (10494910), Simone Tomasi (139458), Livia Tomasini (10494913), Xiaoxu Yang (673521), Bo Zhou (15092), Schahram Akbarian (117762), Laurel L. Ball (10494916), Sara Bizzotto (10138543), Sarah B. Emery (3244203), Ryan Doan (572108), Liana Fasching (10494919), Yeongjun Jang (146006), David Juan (19252), Esther Lizano (5986972), Lovelace J. Luquette (10494922), John B. Moldovan (10494925), Rujuta Narurkar (10494928), Matthew T. Oetjens (9635214), Rachel E. Rodin (10138540), Shobana Sekar (4243036), Joo Heon Shin (7432022), Eduardo Soriano (196519), Richard E. Straub (10494931), Weichen Zhou (6004454), Andrew Chess (63935), Joseph G. Gleeson (10494934), Tomas Marquès-Bonet (10494937), Peter J. Park (8186340), Mette A. Peters (6641051), Jonathan Pevsner (15767), Christopher A. Walsh (8667276), Daniel R. Weinberger (9283256), Flora M. Vaccarino (10494940), John V. Moran (10494943), Alexander E. Urban (10494946), Jeffrey M. Kidd (7465493), Ryan E. Mills (10494949), Alexej Abyzov (9637287)

مصطلحات موضوعية: Genetics, mosaic SNVs, Brain Somatic Mosaicism Network, nucleotide variants, DNA repair, single-nucleotide variants, bulk DNA samples, brain regions, mosaic variants, Somatic mosaicism, non-cancerous tissues, brain tissue Abstract Background Po., variant allele fractions, Comprehensive identification, dural fibroblasts, dura mater, multi-institutional study, DNA replication, cell lineage trees, dorsolateral prefrontal cortex, whole-genome sequencing data

Relation: https://figshare.com/articles/journal_contribution/Additional_file_6_of_Comprehensive_identification_of_somatic_nucleotide_variants_in_human_brain_tissue/14337781

الاتاحة: https://doi.org/10.6084/m9.figshare.14337781.v1

المؤلفون: Karen E. Wain, Kasia Tolwinski, Emily Palen, Alexis R. Heidlebaugh, Karahlyn Holdren, Lauren Kasparson Walsh, Matthew T. Oetjens, David H. Ledbetter, Christa Lese Martin

المصدر: Journal of Personalized Medicine; Volume 11; Issue 5; Pages: 365

مصطلحات موضوعية: genomic screening, personal utility, neuropsychiatric disorders, brain disorders, copy number variant

وصف الملف: application/pdf

Relation: https://dx.doi.org/10.3390/jpm11050365

الاتاحة: https://doi.org/10.3390/jpm11050365

المؤلفون: Hermela, Shimelis, Matthew T, Oetjens, Lauren K, Walsh, Karen E, Wain, Masa, Znidarsic, Scott M, Myers, Brenda M, Finucane, David H, Ledbetter, Christa Lese, Martin

المصدر: American Journal of Psychiatry. 180:65-72

مصطلحات موضوعية: Psychiatry and Mental health

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59fd15e1b0b944bc8dd2df1e47e1e624
https://doi.org/10.1176/appi.ajp.22010062

المؤلفون: Matthew T Oetjens, Jonathan Z Luo, Alexander Chang, Joseph B Leader, Dustin N Hartzel, Bryn S Moore, Natasha T Strande, H Lester Kirchner, David H Ledbetter, Anne E Justice, David J Carey, Tooraj Mirshahi

المصدر: PLoS ONE, Vol 15, Iss 11, p e0242182 (2020)

مصطلحات موضوعية: Medicine, Science

Relation: https://doi.org/10.1371/journal.pone.0242182; https://doaj.org/toc/1932-6203; https://doaj.org/article/d7be12c3bdfc4e388db8c5c87684a9ab

الاتاحة: https://doi.org/10.1371/journal.pone.0242182
https://doaj.org/article/d7be12c3bdfc4e388db8c5c87684a9ab

المؤلفون: Juliann M. Savatt, Matthew T. Oetjens, Scott M. Myers, Brenda M. Finucane

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics. 25(1)

مصطلحات موضوعية: Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7182efea3f085a97eb10b5bcee3b719
https://pubmed.ncbi.nlm.nih.gov/36609148

المؤلفون: Juliann M. Savatt, Hermela Shimelis, Andres Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter, Christa Lese Martin, Scott M. Myers, Brenda M. Finucane

المصدر: Genet Med

مصطلحات موضوعية: Birt-Hogg-Dube Syndrome, Lung Diseases, Phenotype, Cysts, Proto-Oncogene Proteins, Tumor Suppressor Proteins, Humans, Pneumothorax, Delivery of Health Care, Skin Diseases, Genetics (clinical), Article, Kidney Neoplasms

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21b4e1a98407abc84d711a3587c3cf45
https://europepmc.org/articles/PMC9703446/

المؤلفون: Alexander S Berry, Laney Jones, Amy C Sturm, Samuel Gidding, Matthew T Oetjens

المصدر: Circulation. 145

مصطلحات موضوعية: Physiology (medical), Cardiology and Cardiovascular Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b4d8acaa3ab57632864fa13cbee0ea40
https://doi.org/10.1161/circ.145.suppl_1.068

المؤلفون: Juliann M. Savatt, Hermela Shimelis, Andres Moreno-De-Luca, Natasha T. Strande, Matthew T. Oetjens, David H. Ledbetter, Christa Lese Martin, Scott M. Myers, Brenda M. Finucane

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f449511555116e51b68ba084b6dc7e45
https://doi.org/10.1101/2022.01.31.22269926

المؤلفون: Alexander S. F. Berry, Brenda M. Finucane, Scott M. Myers, Angela Abril, H. Lester Kirchner, David H. Ledbetter, Christa Lese Martin, Matthew T. Oetjens

المصدر: JAMA. 329:235

مصطلحات موضوعية: General Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::da2c141385ed96d8aa6b94268f90a532
https://doi.org/10.1001/jama.2022.23897

المؤلفون: Evan Maxwell, Lukas Habegger, David H. Ledbetter, S.M. Myers, Christa Leese Martin, H L Kirchner, A. Johns, Brenda M Finucane, Matthew T. Oetjens, Jeffrey G. Reid, C. Fisher

المصدر: Genet Med

مصطلحات موضوعية: Adult, medicine.medical_specialty, DNA Copy Number Variations, business.industry, Patient Acceptance of Health Care, Article, Cohort Studies, Healthcare utilization, Prevalence, Medicine, Humans, Copy-number variation, business, Psychiatry, Child, Delivery of Health Care, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeccd13149c410506f7d7f2a8e8eea46
https://europepmc.org/articles/PMC8901449/

المؤلفون: M. A. Kelly, Amy C. Sturm, Christa Lese Martin, Matthew T. Oetjens, David H. Ledbetter

المصدر: Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Nature Communications

مصطلحات موضوعية: Male, 0301 basic medicine, Multifactorial Inheritance, Apolipoprotein B, Turner Syndrome, General Physics and Astronomy, Chromosome Disorders, Trisomy, Familial hypercholesterolemia, Quantitative trait, Body Mass Index, Hypobetalipoproteinemias, 0302 clinical medicine, Chromosome Duplication, XYY Karyotype, Genetics research, lcsh:Science, Sex Chromosome Aberrations, Genetics, education.field_of_study, Multidisciplinary, biology, Medical genetics, Middle Aged, embryonic structures, symbols, Receptor, Melanocortin, Type 4, Female, Chromosome Deletion, Proprotein Convertase 9, Science, Sex Chromosome Disorders of Sex Development, Population, Article, General Biochemistry, Genetics and Molecular Biology, Hyperlipoproteinemia Type II, 03 medical and health sciences, symbols.namesake, Klinefelter Syndrome, Rare Diseases, Intellectual Disability, Genetic variation, medicine, Humans, Obesity, Autistic Disorder, education, Apolipoproteins B, Genetic association, Chromosomes, Human, X, PCSK9, Rare variants, Cholesterol, LDL, General Chemistry, Melanocortin 4 Receptor Deficiency, medicine.disease, Body Height, 030104 developmental biology, Receptors, LDL, biology.protein, Mendelian inheritance, lcsh:Q, Chromosomes, Human, Pair 16, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56db2a15b70185ed9796798dae542b7f
https://doaj.org/article/96dda06cd3764488a3d966497943e622

المؤلفون: Karahlyn Holdren, Karen E. Wain, Christa Lese Martin, Kasia Tolwinski, Emily Palen, David H. Ledbetter, Lauren Kasparson Walsh, Alexis R Heidlebaugh, Matthew T. Oetjens

المصدر: Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 11, Iss 365, p 365 (2021)
Volume 11
Issue 5

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Genetic counseling, Population, Medicine (miscellaneous), 030105 genetics & heredity, Grounded theory, Article, 03 medical and health sciences, Health care, medicine, copy number variant, education, Psychiatry, Exome, education.field_of_study, business.industry, brain disorders, neuropsychiatric disorders, 030104 developmental biology, genomic screening, personal utility, Cohort, Community health, Learning disability, Medicine, medicine.symptom, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b988cf7639fbd65b3885cf411835c95f
https://pubmed.ncbi.nlm.nih.gov/34062946

المؤلفون: Sean J, Jurgens, Seung Hoan, Choi, Valerie N, Morrill, Mark, Chaffin, James P, Pirruccello, Jennifer L, Halford, Lu-Chen, Weng, Victor, Nauffal, Carolina, Roselli, Amelia W, Hall, Matthew T, Oetjens, Braxton, Lagerman, David P, vanMaanen, Krishna G, Aragam, Kathryn L, Lunetta, Christopher M, Haggerty, Steven A, Lubitz, Sarah E, Wolf

المصدر: Nature genetics. 54(3)

مصطلحات موضوعية: Diabetes Mellitus, Type 2, Cardiovascular Diseases, Genetic Variation, Humans, Genetic Predisposition to Disease, Carrier Proteins, United Kingdom, Biological Specimen Banks

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::9575d3d1cb7dc82f32a25bdfc80e1674
https://pubmed.ncbi.nlm.nih.gov/35177841