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recessive

Synonyms

Adjective

1. recessionary

2. financial condition, economic condition, recessive

Usage
Classic recessive-or-dominant gene dynamics may not be so simple - Stanford Report
AAV gene therapy for autosomal recessive deafness 9: a single-arm trial - Nature
Sex differences in behavioral measures of anxiety in a recessive gene knockout ( Pink1 - Frontiers
Developing Imaging Biomarkers for Autosomal Recessive Polycystic Kidney Disease - Cleveland Clinic
Prademagene zamikeracel for recessive dystrophic epidermolysis bullosa wounds (VIITAL): a two-centre, randomised, open-label, intrapatient-controlled phase 3 trial - The Lancet
Human genetic disease - Autosomal Dominant, Inheritance, Genes - Britannica
Recessive Genes May Quietly Shape Health, Learning, and Fertility - Neuroscience News
Teaching NeuroImage: Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Syndrome - Neurology® Journals
Autosomal Recessive Cerebellar Ataxias: Translating Genes to Therapies - Fogel - 2025 - Annals of Neurology - Wiley Online Library
Dominant Recessive Allele | Elementary STEM Club - U.OSU
Natural history study of recessive dystrophic epidermolysis bullosa wounds and patient reported outcomes using mobile application home photography | Scientific Reports - Nature
Micropulse transscleral cyclophotocoagulation in the treatment of autosomal recessive bestrophinopathy combined with angle closure glaucoma: a case report - Frontiers
Prevalence of common autosomal recessive and X-linked conditions in pregnant women in Vietnam: a cross-sectional study - Nature
Heart dysfunction in a rat model with autosomal recessive polycystic kidney disease - Wiley
Reproductive and cognitive phenotypes in carriers of recessive pathogenic variants - Nature
Diagnostic whole exome sequencing in presumably autosomal recessive inherited retinal dystrophies in an Iranian population - Nature
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome | European Journal of Human Genetics - Nature
Clinical experience of the expanded carrier screening for recessive genetic diseases in a large cohort study in Southern central China - Nature
Preliminary evidence for enhanced auditory cortex activation and mental development after gene therapy in children with autosomal recessive deafness 9 - Nature
Saturation genome editing of RNU4-2 reveals distinct dominant and recessive neurodevelopmental disorders - medRxiv
A robust pipeline for ranking carrier frequencies of autosomal recessive and X-linked Mendelian disorders - Nature
Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations - Nature
Carrier screening for recessive disorders - Nature
Prevalence of common autosomal recessive mutation carriers in women in the Southern Vietnam following the application of expanded carrier screening - Nature
Bilateral gene therapy in children with autosomal recessive deafness 9: single-arm trial results - Nature
AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial - The Lancet
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality - Nature
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy - Nature
In vivo topical gene therapy for recessive dystrophic epidermolysis bullosa: a phase 1 and 2 trial - Nature
The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study - Nature
Identification of biallelic POLA2 variants in two families with an autosomal recessive telomere biology disorder - Nature
Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss - Nature
Autosomal recessive cerebellar ataxias: a diagnostic classification approach according to ocular features - Frontiers
In vivo photoreceptor base editing ameliorates rhodopsin-E150K autosomal-recessive retinitis pigmentosa in mice - PNAS
Uncovering recessive alleles in rare Mendelian disorders by genome sequencing of 174 individuals with monoallelic pathogenic variants | European Journal of Human Genetics - Nature
Rare, recessive autism mutations offer clues to the condition - Boston Children's Answers
Most new recessive developmental disorder diagnoses lie within known genes, say scientists - Medical Xpress
Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes | Human Genome Variation - Nature
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation - Nature
Design of efficacious somatic cell genome editing strategies for recessive and polygenic diseases - Nature
INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex - Nature
Diagnostic elusiveness of pathogenic variants in cases of autosomal recessive diseases - Nature
Recessive TMOD1 mutation causes childhood cardiomyopathy - Communications Biology - Nature
A spectrum of clinical severity of recessive titinopathies in prenatal - Frontiers
Autosomal Recessive Primary Microcephaly: Not Just a Small Brain - Frontiers
Recessive cerebellar and afferent ataxias — clinical challenges and future directions - Nature
Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal model - Nature
Elusive variants in autosomal recessive disease: how can we improve timely diagnosis? - Nature
An autosomal recessive form of Alagille-like syndrome that is not linked to JAG1 - Nature
Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice - Science | AAAS
The majority of autosomal recessive nanophthalmos and posterior microphthalmia can be attributed to biallelic sequence and structural variants in MFRP and PRSS56 - Nature
Genome-wide recessive genetic screening in mammalian cells with a lentiviral CRISPR-guide RNA library - Nature
Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach - Frontiers
Heterozygous Genetic Variants in Autosomal Recessive Genes of the Leptin-Melanocortin Signalling Pathway Are Associated With the Development of Childhood Obesity - Frontiers
Recessive COL4A2 Mutation Leads to Intellectual Disability, Epilepsy, and Spastic Cerebral Palsy - Neurology® Journals
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden - Nature
SIGMAR1 mutation associated with autosomal recessive Silver-like syndrome - Neurology® Journals
Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants - Nature
Single mutation in recessive gene increases risk of earlier onset Parkinson’s disease - Mayo Clinic News Network
Teaching NeuroImages: Autosomal recessive spastic ataxia of Charlevoix-Saguenay - Neurology® Journals
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis -regulatory variants in CRX-binding regions of SAMD7 - Nature
Compound heterozygous variants of THG1L result in autosomal recessive cerebellar ataxia - Nature
Two specific mutations are prevalent causes of recessive retinitis pigmentosa in North American patients of Jewish ancestry - Nature
Neurodegenerative Disease Risk in Carriers of Autosomal Recessive Disease - Frontiers
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia - Nature
Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia - Rockefeller University Press
Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2 - The New England Journal of Medicine
Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism - Science | AAAS
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families - Nature
OsNPR3.3-dependent salicylic acid signaling is involved in recessive gene xa5 -mediated immunity to rice bacterial blight - Nature
Study links gene to inherited form of autism - The Transmitter
Estimation of the global burden of autosomal recessive rare inborn errors of metabolism - medRxiv
Dominant modifier DFNM1 suppresses recessive deafness DFNB26 - Nature
Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS - Nature
Recessive and sex-dependent genetic effects in primary hypertension - medRxiv
Understanding recessive disease risk in multi-ethnic populations with different degrees of consanguinity - Wiley Online Library
Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs - Frontiers
Recessive gene disruptions in autism spectrum disorder - Nature
Myasthenic congenital myopathy from recessive mutations at a single residue in NaV1.4 - Neurology® Journals
Is it time to report carrier state for recessive disorders in every microarray analysis?—A pilot model based on hearing loss genes deletions - Nature
Expanding the Allelic Heterogeneity of ANO10 -Associated Autosomal Recessive Cerebellar Ataxia - Neurology® Journals
Mutation-dependent recessive inheritance of NPHS2 -associated steroid-resistant nephrotic syndrome - Nature
Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation - Nature
Prediction of recessive inheritance for missense variants in human disease - medRxiv
Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn’s Disease - Nature
Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 gene - Nature
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta - Nature
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes - Nature
A decaploid pitcher plant genome reveals a novel role for recessive subgenomes - Nature
Dominant and recessive gene expression, chapter Two: the molecular mechanism for dominance - INRAE
Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases - PNAS
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2 - Nature
ENPP1 variants associated with autosomal recessive hypophosphatemic rickets type 2: A case from the endocrine teaching clinics - Mayo Clinic
Molecular analysis of the genes causing recessive demyelinating Charcot–Marie–Tooth disease in Japan - Nature
PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells - PNAS
Deep sequencing reveals 50 novel genes for recessive cognitive disorders - Nature
Generation of keratinocytes from normal and recessive dystrophic epidermolysis bullosa-induced pluripotent stem cells - PNAS
Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy - Nature
Bone Marrow Transplantation for Recessive Dystrophic Epidermolysis Bullosa - The New England Journal of Medicine
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis - Nature
Foreign Language Equivalents
Foreign Language Equivalents of 'recessive'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
,   recessivve,   recrssive,   recessve,   recesisve,   recessvie,   recessiv,   recssive,   recessiive,   ecessive,   recessiev,   recessibe,   recesdive,   recesive,   recessivr,   rwcessive,   receasive,   recessivee,   receessive,   tecessive,   recessie,   recessivw,   ercessive,   rexessive,   rceessive,   recesssive,   reccessive,   recedsive,   reecessive,   recesive,   rcessive,   rrecessive,   eecessive,   recesaive,   recessove,   recesssive,   reecssive,   revessive,   recwssive,   recessice,   reessive,   recsesive,   recessuve,   rrcessive
Words Starting with Letter - 'A'
a a battery a billion
a bit a bit much a capella singing
a cappella singing a couple of a few
a fortiori a good deal a great deal
a horizon a hundred a hundred and one
a hundred thousand a hundred times a kempis
a la carte a la mode a level
a little a lot a million
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