Karen Avraham
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Karen Avraham's Degrees
- PhD Genetics Stanford University
Why Is Karen Avraham Influential?
(Suggest an Edit or Addition)According to Wikipedia, Karen B. Avraham is an Israeli-American human geneticist and the first female Dean of the Tel Aviv University's Faculty of Medicine. Born in Canada in 1962, Avraham moved to the US at a young age. Her research focuses on the discovery and characterization of genes responsible for hereditary hearing loss.
Karen Avraham's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Targeted disruption of the mouse Caspase 8 gene ablates cell death induction by the TNF receptors, Fas/Apo1, and DR3 and is lethal prenatally. (1998) (1280)
- Genome-wide, large-scale production of mutant mice by ENU mutagenesis (2000) (696)
- GJB2 mutations and degree of hearing loss: a multicenter study. (2005) (479)
- The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells (1995) (478)
- Transgenic mice with increased Cu/Zn-superoxide dismutase activity: animal model of dosage effects in Down syndrome. (1987) (478)
- Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. (1998) (334)
- A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment (2005) (314)
- Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. (2003) (296)
- Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82. (2010) (279)
- Expert Specification of the ACMG/AMP Variant Interpretation Guidelines for Genetic Hearing Loss (2018) (273)
- Role of myosin VI in the differentiation of cochlear hair cells. (1999) (260)
- Beethoven, a mouse model for dominant, progressive hearing loss DFNA36 (2002) (242)
- From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30 (2002) (231)
- MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. (2001) (216)
- The Notch ligand Jagged1 is required for inner ear sensory development (2001) (214)
- Down's syndrome: Abnormal neuromuscular junction in tongue of transgenic mice with elevated levels of human Cu/Zn-superoxide dismutase (1988) (206)
- Hearing loss: mechanisms revealed by genetics and cell biology. (2009) (197)
- Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families (2011) (195)
- Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene. (2004) (191)
- MicroRNAs are essential for development and function of inner ear hair cells in vertebrates (2009) (175)
- USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses (2002) (166)
- The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population (1999) (158)
- Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22 (2002) (155)
- Hearing Impairment: A Panoply of Genes and Functions (2010) (152)
- The LINC complex is essential for hearing. (2013) (151)
- The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced products. (1996) (144)
- Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East (2002) (144)
- Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India (2003) (140)
- Transgenic mice with expression of elevated levels of copper-zinc superoxide dismutase in the lungs are resistant to pulmonary oxygen toxicity. (1991) (140)
- Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment. (2001) (124)
- Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss. (2006) (116)
- Unconventional myosins and the genetics of hearing loss. (1999) (112)
- Mouse models to study inner ear development and hereditary hearing loss. (2007) (111)
- Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss. (2003) (108)
- Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type III (2003) (104)
- Genetics of Hearing Loss: Syndromic. (2015) (103)
- Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice. (1997) (100)
- Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51. (2010) (96)
- Cell damage by excess CuZnSOD and Down's syndrome. (1994) (89)
- A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome. (2003) (89)
- Gfi1 and Gfi1b act equivalently in haematopoiesis, but have distinct, non‐overlapping functions in inner ear development (2006) (89)
- Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families (2010) (87)
- A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein. (2002) (86)
- A Myo6 Mutation Destroys Coordination between the Myosin Heads, Revealing New Functions of Myosin VI in the Stereocilia of Mammalian Inner Ear Hair Cells (2008) (84)
- Myosin VI is required for structural integrity of the apical surface of sensory hair cells in zebrafish. (2004) (84)
- Down's syndrome: morphological remodelling and increased complexity in the neuromuscular junction of transgenic CuZn-superoxide dismutase mice (1991) (82)
- High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim. (1999) (80)
- SPIKE: a database of highly curated human signaling pathways (2010) (78)
- Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation*♦ (2010) (77)
- Integration of Transcriptomics, Proteomics, and MicroRNA Analyses Reveals Novel MicroRNA Regulation of Targets in the Mammalian Inner Ear (2011) (77)
- Mapping of unconventional myosins in mouse and human. (1996) (76)
- Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locus. (2006) (65)
- Reduced changes in protein compared to mRNA levels across non-proliferating tissues (2017) (65)
- Diminished serotonin uptake in platelets of transgenic mice with increased Cu/Zn‐superoxide dismutase activity. (1989) (63)
- Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system (2007) (61)
- The DFNA15 Deafness Mutation Affects POU4F3 Protein Stability, Localization, and Transcriptional Activity (2003) (58)
- Molecular diversity of the SCG10/stathmin gene family in the mouse. (1993) (58)
- Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population (2006) (57)
- MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness (2009) (55)
- Hearing loss: a common disorder caused by many rare alleles (2010) (55)
- Hereditary hearing loss: From human mutation to mechanism (2011) (53)
- Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene. (1996) (52)
- Premature aging changes in neuromuscular junctions of transgenic mice with an extra human CuZnSOD gene: A model for tongue pathology in Down's syndrome (1988) (51)
- A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment (2004) (51)
- Down syndrome clinical symptoms are manifested in transfected cells and transgenic mice overexpressing the human Cu/Zn-superoxide dismutase gene. (1990) (51)
- CLRN1 Is Nonessential in the Mouse Retina but Is Required for Cochlear Hair Cell Development (2009) (50)
- Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy (2014) (47)
- cDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominantly expressed in the auditory organs. (1995) (47)
- Tailchaser (Tlc): A new mouse mutation affecting hair bundle differentiation and hair cell survival (1999) (44)
- Connexin-associated deafness and speech perception outcome of cochlear implantation. (2006) (43)
- microRNAs: the art of silencing in the ear (2012) (43)
- Mouse Models for Deafness: Lessons for the Human Inner Ear and Hearing Loss (2003) (42)
- A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA (2011) (41)
- Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84 (2010) (40)
- Therapeutics of hearing loss: expectations vs reality. (2005) (39)
- Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways (2014) (39)
- Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity. (2004) (39)
- Promoting Arab and Israeli cooperation: peacebuilding through health initiatives (2005) (37)
- Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing (2013) (37)
- MicroRNAs in sensorineural diseases of the ear (2013) (36)
- Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia. (2003) (34)
- Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel (2019) (34)
- Connexins in Hearing Loss: A Comprehensive Overview (2005) (34)
- Mouse models for human deafness: current tools for new fashions. (2002) (34)
- Deafness Genes in Israel: Implications for Diagnostics in the Clinic (2009) (34)
- High-throughput sequencing to decipher the genetic heterogeneity of deafness (2012) (33)
- Mice with vestibular deficiency display hyperactivity, disorientation, and signs of anxiety (2009) (31)
- Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor. (2000) (30)
- Expression of manganese superoxide dismutase is not altered in transgenic mice with elevated level of copper-zinc superoxide dismutase. (1993) (29)
- The GPSM2/LGN GoLoco motifs are essential for hearing (2016) (29)
- The R245X Mutation of PCDH15 in Ashkenazi Jewish Children Diagnosed with Nonsyndromic Hearing Loss Foreshadows Retinitis Pigmentosa (2004) (29)
- MuD: an interactive web server for the prediction of non-neutral substitutions using protein structural data (2010) (29)
- Time-dependent Gene Expression Analysis of the Developing Superior Olivary Complex* (2013) (29)
- miR-96 is required for normal development of the auditory hindbrain (2018) (28)
- The acquisition of mechano‐electrical transducer current adaptation in auditory hair cells requires myosin VI (2016) (27)
- Functional Characterization of Pendrin Mutations Found in the Israeli and Palestinian Populations (2011) (27)
- Collaborative genomics for human health and cooperation in the Mediterranean region (2010) (27)
- Mechanical forces drive ordered patterning of hair cells in the mammalian inner ear (2020) (26)
- Insights into inner ear-specific gene regulation: Epigenetics and non-coding RNAs in inner ear development and regeneration. (2017) (25)
- Murine chromosomal location of eight members of the hepatocyte nuclear factor 3/fork head winged helix family of transcription factors. (1995) (25)
- Murine chromosomal location of four hepatocyte-enriched transcription factors: HNf-3α, HNF-3β, HNF-3γ, and HNF-4 (1992) (25)
- Ankrd6 is a mammalian functional homolog of Drosophila planar cell polarity gene diego and regulates coordinated cellular orientation in the mouse inner ear. (2014) (25)
- microRNA-224 regulates Pentraxin 3, a component of the humoral arm of innate immunity, in inner ear inflammation. (2014) (24)
- Mapping of the mouse homolog of the human runt domain gene, AML2, to the distal region of mouse chromosome 4. (1995) (24)
- An ENU-induced mutation in AP-2α leads to middle earand ocular defects in Doarad mice (2004) (23)
- Mapping of murine fibroblast growth factor receptors refines regions of homology between mouse and human chromosomes. (1994) (23)
- Audiological Manifestations and Features of Connexin 26 Deafness (2003) (22)
- Egr2::Cre Mediated Conditional Ablation of Dicer Disrupts Histogenesis of Mammalian Central Auditory Nuclei (2012) (22)
- DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory sensory epithelium (2018) (20)
- A novel SLC26A4 (PDS) deafness mutation retained in the endoplasmic reticulum. (2008) (20)
- Genomic analysis of inherited hearing loss in the Palestinian population (2020) (20)
- Murine chromosomal location of four class III POU transcription factors. (1993) (20)
- Integration of Human and Mouse Genetics Reveals Pendrin Function in Hearing and Deafness (2011) (20)
- Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness (2020) (19)
- Genetics of hearing loss in the Arab population of Northern Israel (2018) (19)
- Genome-wide identification and expression profiling of long non-coding RNAs in auditory and vestibular systems (2017) (19)
- Cytoplasmic Mislocalization of POU3F4 Due to Novel Mutations Leads to Deafness in Humans and Mice (2013) (18)
- Auditory Performance in Recovered SARS-COV-2 Patients (2020) (18)
- Chromosomal organization and transcriptional regulation of human GEM and localization of the human and mouse GEM loci encoding an inducible Ras-like protein. (1995) (17)
- Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness (2014) (17)
- Genomic structure of the human unconventional myosin VI gene. (2000) (17)
- The Structural Context of Disease-causing Mutations in Gap Junctions* (2006) (16)
- Auditory and Vestibular Mouse Mutants: Models For Human Deafness (2000) (15)
- Genomic advances for gene discovery in hereditary hearing loss (2012) (14)
- Atypical Auditory Brainstem Response and Protein Expression Aberrations Related to ASD and Hearing Loss in the Adnp Haploinsufficient Mouse Brain (2019) (14)
- Hear come more genes! (1998) (14)
- Anti-apoptotic factor z-Val-Ala-Asp-fluoromethylketone promotes the survival of cochlear hair cells in a mouse model for human deafness (2010) (13)
- The Genetics of Hearing Loss (2015) (13)
- MuD: an interactive web server for the prediction of non-neutral substitutions using protein structural data (2010) (12)
- Positional-candidate cloning of genes from mouse mutants. (2001) (12)
- Striatin is a novel modulator of cell adhesion (2018) (12)
- An ENU-induced mutation in AP-2alpha leads to middle ear and ocular defects in Doarad mice. (2004) (12)
- The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestry. (2014) (12)
- Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1 (2020) (12)
- Clinical symptoms of Down syndrome are manifested in transgenic mice overexpressing the human Cu/Zn-superoxide dismutase gene. (1990) (11)
- Progressive vestibular mutation leads to elevated anxiety (2010) (11)
- Balance deficit enhances anxiety and balance training decreases anxiety in vestibular mutant mice (2015) (11)
- Genetic Therapies for Hearing Loss: Accomplishments and Remaining Challenges (2019) (11)
- Advances in genetic diagnostics for hereditary hearing loss (2013) (11)
- Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel (2018) (10)
- United by Hope, Divided by Access: Country Mapping of COVID-19 Information Accessibility and Its Consequences on Pandemic Eradication (2021) (10)
- Computational analysis of mRNA expression profiling in the inner ear reveals candidate transcription factors associated with proliferation, differentiation, and deafness (2018) (9)
- Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss (2021) (9)
- Rescue from hearing loss in Usher's syndrome. (2013) (8)
- Use of transgenic animals to study disease models: hyperoxic lung injury and ischemic acute renal failure in "high SOD" mice. (1992) (8)
- Homozygote loss-of-function variants in the human COCH gene underlie hearing loss (2020) (7)
- Deafness: Sounds from the cochlea (1997) (7)
- Prospects for Gene Therapy in Hearing Loss (2003) (7)
- A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing (2021) (6)
- Inherited Connexin Mutations Associated with Hearing Loss (2001) (6)
- Expression pattern of cochlear microRNAs in the mammalian auditory hindbrain (2020) (6)
- Murine chromosomal location of four hepatocyte-enriched transcription factors: HNF-3 alpha, HNF-3 beta, HNF-3 gamma, and HNF-4. (1992) (6)
- Developmental Genes Associated with Human Hearing Loss (2005) (6)
- A "Tric" to tighten cell-cell junctions in the cochlea for hearing. (2013) (6)
- A mouse model for benign paroxysmal positional vertigo with genetic predisposition for displaced otoconia (2020) (6)
- Shear forces drive precise patterning of hair cells in the mammalian inner ear (2019) (5)
- The Genomics of Auditory Function and Disease. (2022) (5)
- Hearing loss patterns after cochlear implantation via the round window in an animal model. (2016) (5)
- The inner ear phenotype of Volchok (Vlk): An ENU-induced mouse model for CHARGE syndrome (2010) (4)
- Genetics of Deafness: Recent Advances and Clinical Implications (2002) (4)
- The clinical presentation of DFNA15/POU4F3. (2002) (4)
- Striatin Is Required for Hearing and Affects Inner Hair Cells and Ribbon Synapses (2020) (4)
- Identification and characterization of key long non-coding RNAs in the mouse cochlea (2020) (4)
- The noncoding genome and hearing loss (2021) (4)
- Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene (2022) (4)
- [INNOVATIONS IN RESEARCH OF HEREDITARY DEAFNESS]. (2020) (3)
- Single cell analysis of the inner ear sensory organs (2017) (3)
- Motors, channels and the sounds of silence (1997) (3)
- Erratum: Molecular diversity of the SCG10/stathmin gene family in the mouse (Genomics (1993) 18:2 (360-373)) (1994) (3)
- A lesson from COVID-19 on inaccessibility of web-based information for disabled populations worldwide (2020) (3)
- Ankrd 6 is a mammalian functional homolog of Drosophila planar cell polarity gene diego and regulates coordinated cellular orientation in the mouse inner ear (3)
- PNPT1, MYO15A, PTPRQ, and SLC12A2‐associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern India (2021) (3)
- THE COMPLEXITY OF HEARING LOSS FROM A GENETICS PERSPECTIVE (2004) (2)
- Future Trends and Potential for Treatment of Sensorineural Hearing Loss (2006) (2)
- Molecular Motors in Sensory Defects (2004) (2)
- A Nesprin-4/kinesin-1 cargo model for nuclear positioning in cochlear outer hair cells (2021) (2)
- Factor V , tissue factor pathway inhibitor , and east Texas bleeding disorder (2018) (2)
- Human Gene Discovery for Understanding Development of the Inner Ear and Hearing Loss (2014) (2)
- Apparent phenotypic anticipation in autosomal dominant connexin 26 deafness (2014) (2)
- High-throughput sequencing to decipher the genetic heterogeneity of deafness (2012) (1)
- The long and short: Non-coding RNAs in the mammalian inner ear (2022) (1)
- Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness (2014) (1)
- Modifying with mitochondria (2001) (1)
- Overexpression of the human CuZnSOD gene in transfected cells--implication to Down syndrome. (1987) (1)
- Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways (2014) (1)
- Emerging complexities of the mouse as a model for human hearing loss (2022) (1)
- What's hot about otoferlin (2016) (1)
- POU-Domain Transcription Factors (2003) (1)
- The genetics of deafness: a model for genomic and biological complexity. (2002) (1)
- Molecular Etiology of Deafness and Cochlear Consequences (2013) (1)
- DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory organ of Corti (2018) (1)
- Revealing Global Government Health Website Accessibility Errors During COVID-19 and the Necessity of Digital Equity (2020) (1)
- Program and Abstracts of the 16th Transgenic Technology Meeting (TT2020) (2020) (0)
- The Slc26a4 loop Mouse Model for Pendred’s Syndrome and Nonsyndromic Deafness (2017) (0)
- Editorial Board (2011) (0)
- Homozygote loss-of-function variants in the human COCH gene underlie hearing loss (2020) (0)
- Bats experience age-related hearing loss (presbycusis) (2023) (0)
- Genomic Applications in Audiological Medicine (2014) (0)
- Biochemical , functional , and clinical implications of PP 6 C mutations in melanoma (2014) (0)
- ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (2019) (0)
- DNA methylation dynamics during embryonic development and postnatal maturation of the mouse auditory sensory epithelium (2018) (0)
- Masthead (2016) (0)
- Molecular Features of SLC26A4 Common Variant p.L117F (2022) (0)
- Acknowledgement to referees 2002 (2003) (0)
- Genome-wide identification and expression profiling of long non-coding RNAs in auditory and vestibular systems (2017) (0)
- Reprogramming of two induced pluripotent stem cell lines from a heterozygous GRIN2D developmental and epileptic encephalopathy (DEE) patient (BGUi011-A) and from a healthy family relative (BGUi012-A). (2021) (0)
- Sensory Defects Caused by Mutant Motor Proteins (2008) (0)
- Israel Society for Auditory Research (ISAR): 2014 Annual Scientific Conference (2014) (0)
- Masthead (2011) (0)
- Reduced changes in protein compared to mRNA levels across non-proliferating tissues (2017) (0)
- Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder (2021) (0)
- Molecular genetic characterization of the deaf Snell`s waltzer mouse (1994) (0)
- Correction: ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs (2019) (0)
- Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss. (2023) (0)
- Acknowledgement of Reviewers 2014 (2015) (0)
- Atypical Auditory Brainstem Response and Protein Expression Aberrations Related to ASD and Hearing Loss in the Adnp Haploinsufficient Mouse Brain (2019) (0)
- Stereocilia Start to Develop Normally , but Then Fuse Together to Form Giant Stereocilia (1999) (0)
- The biological basis for autosomal dominant nonsyndromic hearing loss DFNA15: expression, DNA binding and transcription properties. (2000) (0)
- Computational analysis of mRNA expression profiling in the inner ear reveals candidate transcription factors associated with proliferation, differentiation, and deafness (2018) (0)
- The GPSM2/LGN GoLoco motifs are essential for hearing (2015) (0)
- A homozygous AP3D1 missense variant in patients with sensorineural hearing loss as the leading manifestation. (2022) (0)
- A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing (2021) (0)
- Breaking Barriers: (2018) (0)
- Noise stresses the junctions to deaf (2009) (0)
- 2 Genetics of Hearing Loss (2017) (0)
- Reviewer Acknowledgment 2014 (2014) (0)
- Genes and Mutations in Hearing Impairment (2002) (0)
- Repair of Noise-Induced Damage to Stereocilia F-actin Cores is Facilitated by XIRP2 (2021) (0)
- Israel Society for Auditory Research (ISAR): 2013 Annual Scientific Conference (2013) (0)
- Genetic and phenotypic heterogeneity in PNPT1, MYO15A, PTPRQ and SLC12A2 variants detected among hearing impaired assortative mating families in Southern India (2021) (0)
- Masthead (2011) (0)
- Genetics of hearing loss in the Arab population of Northern Israel (2018) (0)
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Karen Avraham is affiliated with the following schools:
