Author details

Full Name

Jianhong Hu

Affiliation

ORCID

Career Start Year

1992

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37537399	The master growth regulator DELLA binding to histone H2A is essential for DELLA-mediated global transcription regulation.	Nat Plants	2023
36332373	NGF regulates sertoli cell growth and prevents LPS-induced junction protein damage via PI3K/AKT/NFÎºB signaling.	Theriogenology	2023
36332369	FSH-inhibited autophagy protects against oxidative stress in goat Sertoli cells through p62-Nrf2 pathway.	Theriogenology	2023
37790445	Genetic Sex Validation for Sample Tracking in Clinical Testing.	Res Sq	2023
36740243	SPINDLY O-fucosylates nuclear and cytoplasmic proteins involved in diverse cellular processes in plants.	Plant Physiol	2023
37366551	Circulating tumor DNA sequencing of pediatric solid and brain tumor patients: An institutional feasibility study.	Pediatr Hematol Oncol	2023
36924128	Plasmonic nanorod probes' journey inside plant cells for SERS sensing and multimodal imaging.		2023
37037878	Four class A AUXIN RESPONSE FACTORs promote tomato fruit growth despite suppressing fruit set.		2023
35331649	Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.	Genet Med	2022
35713195	Clinical and molecular features of pediatric cancer patients with Lynch syndrome.	Pediatr Blood Cancer	2022
36054313	Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism.	Hum Mutat	2022
34582790	High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population.	Am J Hum Genet	2021
33644933	Phenotypic and protein localization heterogeneity associated with AHDC1 pathogenic protein-truncating alleles in Xia-Gibbs syndrome.	Hum Mutat	2021
34301805	Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplant.	Life Sci Alliance	2021
33863344	Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.	Genome Biol	2021
33217343	Molecular Features of Cancers Exhibiting Exceptional Responses to Treatment.	Cancer Cell	2021
34711608	Transcriptional Reprogramming Differentiates Active from Inactive ESR1 Fusions in Endocrine Therapy-Refractory Metastatic Breast Cancer.	Cancer Res	2021
34950897	AHDC1 missense mutations in Xia-Gibbs syndrome.	HGG Adv	2021
34651095	Durable Response to Larotrectinib in a Child With Histologic Diagnosis of Recurrent Disseminated Ependymoma Discovered to Harbor an <i>NTRK2</i> Fusion: The Impact of Integrated Genomic Profiling.	JCO Precis Oncol	2021
34363016	Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications.	Genet Med	2021
34748517	The first central precocious puberty proteomic profiles revealed multiple metabolic networks and novel key disease-associated proteins.	Aging	2021
31378813	Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol).	Int J Epidemiol	2020
32233023	Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.	Am J Med Genet A	2020
32767738	Community-based recruitment and exome sequencing indicates high diagnostic yield in adults with intellectual disability.	Mol Genet Genomic Med	2020
32722525	Next Generation Sequencing of 134 Children with Autism Spectrum Disorder and Regression.	Genes (Basel)	2020
30827684	Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2.	Cell	2019
30622330	Genetic architecture of laterality defects revealed by whole exome sequencing.	Eur J Hum Genet	2019
31230720	The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance.	Am J Hum Genet	2019
30867694	Downregulation of microRNA-374a predicts poor prognosis in human glioma.	Experimental and Therapeutic Medicine (discontinued)	2019
31516582	Elevated CD44 expression predicts poor prognosis in patients with low-grade glioma.	Oncology Letters	2019
30890783	Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.	Genet Med	2019
31321455	MHC genotyping from rhesus macaque exome sequences.	Immunogenetics	2019
29232328	Novel CYP2A6 diplotypes identified through next-generation sequencing are associated with in-vitro and in-vivo nicotine metabolism.	Pharmacogenet Genomics	2018
28813618	Whole-Exome Sequencing Identifies Novel Variants for Tooth Agenesis.	J Dent Res	2018
30165405	Elucidating the molecular pathogenesis of glioma: integrated germline and somatic profiling of a familial glioma case series.	Neuro Oncol	2018
30104574	Identification and functional study of a mild allele of SlDELLA gene conferring the potential for improved yield in tomato.	Scientific Reports	2018
30008445	The Interaction between DELLA and ARF/IAA Mediates Crosstalk between Gibberellin and Auxin Signaling to Control Fruit Initiation in Tomato.	Plant Cell	2018
29436111	A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis.	Am J Med Genet A	2018
28244988	The Arabidopsis O-fucosyltransferase SPINDLY activates nuclear growth repressor DELLA.	Nat Chem Biol	2017
28798025	Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.	Circ Cardiovasc Genet	2017
28973083	Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.	JAMA Pediatr	2017
28327206	Lessons learned from additional research analyses of unsolved clinical exome cases.	Genome Med	2017
27577878	Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.	J Allergy Clin Immunol	2017
28052041	Non-malignant respiratory epithelial cells preferentially proliferate from resected non-small cell lung cancer specimens cultured under conditionally reprogrammed conditions.	Oncotarget	2017
27117591	Novel patient-derived xenograft and cell line models for therapeutic testing of pediatric liver cancer.	J Hepatol	2016
27435318	Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate.	BMC Med Genomics	2016
26804919	Ampullary Cancers Harbor ELF3 Tumor Suppressor Gene Mutations and Exhibit Frequent WNT Dysregulation.	Cell Rep	2016
26882539	An open access pilot freely sharing cancer genomic data from participants in Texas.	Sci Data	2016
26907327	A Toolbox for Herpesvirus miRNA Research: Construction of a Complete Set of KSHV miRNA Deletion Mutants.	Viruses	2016
26773002	O-GlcNAcylation of master growth repressor DELLA by SECRET AGENT modulates multiple signaling pathways in Arabidopsis.	Genes Dev	2016