Faculty

Institution

Unit

Venue

David L Nelson

Professor

Baylor College of Medicine

Affiliations

Baylor College of Medicine Research

David L Nelson is currently serving as a Baylor College Of Medicine Research Professor at Baylor College of Medicine.

Honors

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Experiences

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Education

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David L Nelson

Baylor College of Medicine

Professor

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genetics immunology molecular biology human genetics immune responses genomics molecular genetics neuroscience medical genetics gene expression genetic disorders clinical immunology receptors genome biology immunity (medicine) mammalian biology medicinal research cytokines population genetics immunopathology virus research cellular immune responses vascular biology molecular immunology molecular cell biology neurodevelopmental disorders molecular neurodegeneration immunologic mechanisms cytogenetics heredity knockout mice cloning stem cell research cell death antiviral research molecular basis mucosal immunology genome analysis wiskott-aldrich syndrome cellular therapy cell research nucleic acids genome instability developmental genetics chromosome biology t-regulatory cell antibody engineering medical virology rna biology somatic variant viral pathogenesis immunomodulation mutagenesis lymphocyte development incontinentia pigmenti wiskott-aldrich syndrome protein mouse model neurotransmission immunochemistry immunotoxicology sequence analysis disease gene identification primate behavior primate systematics alternative splicing somatic mosaicism agg interruptions fragile x-related proteins fc receptors x-linked hypogammaglobulinemia initial sequencing monoclonal antibody drosophila model selective iga deficiency neurological disease elevated levels forensic genetics biostatistics human genome genetic analysis gene duplication

Notable Scholarly Works

Notable Federal Grants

Collaborators

Characterization and Visualization of Tandem Repeats at Genome Scale. Nature Biotechnology (2024)

Egor DolzhenkoAdam EnglishHarriet DashnowGuilherme De Sena BrandineTom MokveldWilliam J RowellCaitlin KarniskiZev KronenbergMatt C DanziWarren A CheungChengpeng BiEmily FarrowAaron WengerKhi Pin ChuaVerónica Martínez-CerdeñoTrevor D BartleyPeng JinDavid L NelsonStephan ZuchnerTomi PastinenAaron R QuinlanFritz J SedlazeckMichael A Eberle

genomicsgenome biologybiotechnologygenome scalemolecular biologyvisualizationtandem repeats

Personal Journeys to and in Human Genetics and Dysmorphology. American Journal of Medical Genetics Part A (2024)

Charles E. SchwartzArthur S. AylsworthJudith AllansonAgatino BattagliaJohn C. CareyCynthia J. CurryKay E. DaviesEvan E. EichlerJohn M. GrahamBryan HallJudith G. HallLewis B. HolmesH. Eugene HoymeAlasdair HunterJeffrey InnisJohn JohnsonKim M. Keppler‐NoreuilJules G. LeroyCynthia MooreDavid L. NelsonGiovanni NeriJohn M. OpitzDavid PickettsF. Lucy RaymondStavit Allon ShalevRoger E. StevensonConnie T. R. M. StumpelGrant SutherlandDavid H. ViskochilDavid D. WeaverElaine H. Zackai

personal journeyshuman geneticsgenetics

Resolving the Unsolved: Comprehensive Assessment of Tandem Repeats at Scale. bioRxiv (Cold Spring Harbor Laboratory) (2023)

Egor DolzhenkoAdam EnglishHarriet DashnowGuilherme De Sena BrandineTom MokveldWilliam J. RowellCaitlin KarniskiZev KronenbergMatt C. DanziWarren CheungChengpeng BiEmily FarrowAaron WengerVerónica Martínez-CerdeñoTrevor D BartleyPeng JinDavid NelsonStephan ZuchnerTomi PastinenAaron R. QuinlanFritz J. SedlazeckMichael A Eberle

comprehensive assessmentlaboratory investigationbiostatisticstandem repeatsperformance evaluation

Emerging Therapeutic Strategies for Fragile X Syndrome: Q A. ACS Chemical Neuroscience (2022)

Ghassan AlusiElizabeth Berry-KravisDavid NelsonLauren L. OreficeSam A. Booker

neurologymedicineneuropharmacologytherapeutic strategiesneuroscience

Identification of Psmb5 as a Genetic Modifier of Fragile X–Associated Tremor/Ataxia Syndrome. Proceedings of the National Academy of Sciences (2022)

Ha Eun KongJunghwa LimAlexander LinsalataYunhee KangIndranil MalikEmily G. AllenYiqu CaoLisa ShubeckRich JohnstonYanting HuangYanghong GuXiangxue GuoMichael E. ZwickZhaohui QinThomas S. WingoJorge JuncosDavid L. NelsonMichael P. EpsteinDavid J. CutlerPeter K. ToddStephanie L. ShermanStephen T. WarrenPeng Jin

genomicsneurologydermatologyhost geneticsneurogeneticsgenetic basisgeneticsdisease gene identificationmolecular geneticsmovement disorderspsychiatric geneticshuman geneticsgenetic disordersgenetic modifier

Identification of Psmb5 as a Genetic Modifier of Fragile X-Associated Tremor/Ataxia Syndrome. Proc Natl Acad Sci U S A (2022)

genetic disordersneurogeneticsmolecular neurosciencegeneticsdisease gene identificationmovement disordersmolecular neurodegenerationpsychiatric geneticsmolecular psychiatrymedical geneticsneurosciencegenetic modifier

Intercepting Ire1 Kinase‐Fmrp Signaling Prevents Atherosclerosis Progression. EMBO Molecular Medicine (2022)

Zehra YildirimSabyasachi BabooSyed M HamidAsli E DoganOzlem TufanliSabrina RobichaudChristina EmertonJolene K DiedrichHasan VatandaslarFotis NikolosYanghong GuTakao IwawakiElizabeth TarlingMireille OuimetDavid L NelsonJohn R YatesPeter WalterEbru Erbay

immunologymedicinegene expressionhematologyatherosclerosisvascular biologyhepatologymembrane biologyhealth sciences

Llps of Fxr1 Drives Spermiogenesis by Activating Translation of Stored Mrnas. Science (2022)

Jun-Yan KangZe WenDuo PanYuhan ZhangQing LiAi ZhongXinghai YuYi-Chen WuYu ChenXiangzheng ZhangPeng-Cheng KouJunlan GengYing-Yi WangMin-Min HuaRuiting ZongBiao LiHui-Juan ShiDangsheng LiXiang-Dong FuJinsong LiDavid L. NelsonXuejiang GuoYu ZhouLan-Tao GouYing HuangMo-Fang Liu

cell signalingstored mrnascell biologystem cell researchtranscription factorsmolecular cell biologyreproductive biologylong non-coding rnanucleic acidsfunctional genomicstranscription (biology)mammalian biologyinduced pluripotent stem cellsgene expressiontranscription regulationsystems biologymolecular biologyprotein expressionrna biology

Stephen T. Warren, Ph.D. (1953–2021): A Remembrance. The American Journal of Human Genetics (2022)

David L. NelsonJanelle ClarkKathryn GarberThomas GloverTerry HassoldPeng JinHarry T. OrrStephanie L. ShermanHuda ZoghbiKaren L. Warren

genomicsheredityamerican studiesgeneticsbiologymemoryanthropologyhuman genetics

Ectopic Expression of Cgg-Repeats Alters Ovarian Response to Gonadotropins and Leads to Infertility in a Murine Fmr1 Premutation Model. Hum Mol Genet (2021)

reproductive immunologyreproductive endocrinologyoogenesisreproductive medicinefertilityendocrinologygeneticsreproductive sciencereproductive biologyectopic expressioninfertilitydevelopmental biologyreproductive healthgynecologyovarian cancerfemale reproductive systemovarian hormones

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David L Nelson

Professor

Baylor College of Medicine

Affiliations

Baylor College of Medicine Research

David L Nelson is currently serving as a Baylor College Of Medicine Research Professor at Baylor College of Medicine.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

David L Nelson

Baylor College of Medicine

Professor

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Characterization and Visualization of Tandem Repeats at Genome Scale. Nature Biotechnology (2024)

genomicsgenome biologybiotechnologygenome scalemolecular biologyvisualizationtandem repeats

Personal Journeys to and in Human Genetics and Dysmorphology. American Journal of Medical Genetics Part A (2024)

personal journeyshuman geneticsgenetics

Resolving the Unsolved: Comprehensive Assessment of Tandem Repeats at Scale. bioRxiv (Cold Spring Harbor Laboratory) (2023)

comprehensive assessmentlaboratory investigationbiostatisticstandem repeatsperformance evaluation

Emerging Therapeutic Strategies for Fragile X Syndrome: Q A. ACS Chemical Neuroscience (2022)

Ghassan AlusiElizabeth Berry-KravisDavid NelsonLauren L. OreficeSam A. Booker

neurologymedicineneuropharmacologytherapeutic strategiesneuroscience

Identification of Psmb5 as a Genetic Modifier of Fragile X–Associated Tremor/Ataxia Syndrome. Proceedings of the National Academy of Sciences (2022)

Identification of Psmb5 as a Genetic Modifier of Fragile X-Associated Tremor/Ataxia Syndrome. Proc Natl Acad Sci U S A (2022)

Intercepting Ire1 Kinase‐Fmrp Signaling Prevents Atherosclerosis Progression. EMBO Molecular Medicine (2022)

immunologymedicinegene expressionhematologyatherosclerosisvascular biologyhepatologymembrane biologyhealth sciences

Llps of Fxr1 Drives Spermiogenesis by Activating Translation of Stored Mrnas. Science (2022)

Stephen T. Warren, Ph.D. (1953–2021): A Remembrance. The American Journal of Human Genetics (2022)

David L. NelsonJanelle ClarkKathryn GarberThomas GloverTerry HassoldPeng JinHarry T. OrrStephanie L. ShermanHuda ZoghbiKaren L. Warren

genomicsheredityamerican studiesgeneticsbiologymemoryanthropologyhuman genetics

Ectopic Expression of Cgg-Repeats Alters Ovarian Response to Gonadotropins and Leads to Infertility in a Murine Fmr1 Premutation Model. Hum Mol Genet (2021)

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