Silvia Paracchini

Silvia Paracchini's AcademicInfluence.com Rankings

Silvia Paracchini

Biology

#8205

World Rank

#11244

Historical Rank

Genetics

#1378

World Rank

#1480

Historical Rank

biology Degrees

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Biology

Silvia Paracchini's Degrees

Bachelors Biological Sciences University of Pavia

Why Is Silvia Paracchini Influential?

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According to Wikipedia, Silvia Paracchini FRSE is a geneticist who researches the contribution of genetic variation to neurodevelopmental traits such as dyslexia and human handedness. Education As an undergraduate, Paracchini studied Biological Sciences at the University of Pavia, Italy. During this time she undertook an ERASMUS scholarship project at the Technical University of Denmark. She obtained her DPhil in Human Genetics from the University of Oxford in 2003.

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Silvia Paracchini'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

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. (2006) (279)
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. (2004) (253)
Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects (2010) (231)
A large AZFc deletion removes DAZ3/DAZ4 and nearby genes from men in Y haplogroup N. (2004) (198)
A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa. (2004) (191)
CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment (2009) (176)
DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits (2011) (174)
Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia (2006) (172)
The genetic lexicon of dyslexia. (2007) (155)
Human handedness: A meta-analysis. (2020) (150)
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill (2013) (141)
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. (2008) (139)
Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia (2010) (134)
The genetic relationship between handedness and neurodevelopmental disorders☆ (2014) (132)
PCSK6 is associated with handedness in individuals with dyslexia (2010) (127)
Haplotype-specific expression of exon 10 at the human MAPT locus. (2006) (126)
Genome-wide screening for DNA variants associated with reading and language traits (2014) (108)
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK (2004) (106)
A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene (2009) (101)
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment (2014) (75)
Hierarchical high-throughput SNP genotyping of the human Y chromosome using MALDI-TOF mass spectrometry. (2002) (67)
The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. (2008) (67)
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia (2018) (67)
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort (2013) (62)
Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population (2011) (55)
Advances in Dyslexia Genetics-New Insights Into the Role of Brain Asymmetries. (2016) (54)
The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure (2012) (48)
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia (2020) (45)
Reading and Language Disorders: The Importance of Both Quantity and Quality (2014) (43)
Explorer CMIP and ATP 2 C 2 Modulate Phonological Short-Term Memory in Language Impairment (2009) (43)
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia (2013) (40)
Dissection of genetic associations with language-related traits in population-based cohorts (2011) (39)
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on (2018) (38)
Alternative splicing in the dyslexia-associated gene KIAA0319 (2007) (38)
Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18 (2010) (38)
Y-chromosomal insights into the genetic impact of the caste system in India (2007) (37)
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions (2000) (35)
Copy Number Variation Screen Identifies a Rare De Novo Deletion at Chromosome 15q13.1-13.3 in a Child with Language Impairment (2015) (34)
A Y chromosomal influence on prostate cancer risk: the multi-ethnic cohort study (2003) (31)
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes (2016) (27)
Four meta-analyses across 164 studies on atypical footedness prevalence and its relation to handedness (2020) (24)
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts (2015) (23)
Discovery of 42 genome-wide significant loci associated with dyslexia (2021) (22)
The DCDC2 deletion is not a risk factor for dyslexia (2017) (20)
Insights into Dyslexia Genetics Research from the Last Two Decades (2021) (17)
Different laterality indexes are poorly correlated with one another but consistently show the tendency of males and females to be more left- and right-lateralized, respectively (2020) (15)
Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18 (2010) (14)
Molecular Genetics of Dyslexia (2009) (14)
Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia (2006) (12)
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism (2019) (12)
The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts (2016) (11)
Genetics of Human Handedness and Laterality (2017) (11)
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people (2022) (10)
Recent Advances in Handedness Genetics (2021) (9)
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy (2002) (9)
Quantitative multidimensional phenotypes improve genetic analysis of laterality traits (2021) (7)
Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people (2021) (7)
Human handedness: A meta-analysis (2019) (6)
Handedness in twins: meta-analyses (2021) (6)
Hand preference and Mathematical Learning Difficulties: New data from Greece, the United Kingdom, and Germany and two meta-analyses of the literature (2019) (6)
Different laterality indexes are poorly correlated with one another but consistently show the tendency of males and females to be more left- and right- lateralised, respectively (2019) (5)
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures (2021) (5)
KIAA0319 influences cilia length, cell migration and mechanical cell–substrate interaction (2019) (5)
An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations (2010) (5)
Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample (2019) (4)
Genomic Imprinting As a Window into Human Language Evolution (2019) (4)
The neuronal migration hypothesis of dyslexia: a critical evaluation thirty years on (2018) (3)
The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration (2019) (3)
Genome‐wide association study and polygenic risk score analysis for hearing measures in children (2021) (3)
The dyslexia susceptibility KIAA0319 gene shows a highly specific expression pattern during zebrafish development supporting a role beyond neuronal migration (2018) (3)
TWO Advances in Dyslexia Genetics d New Insights Into the Role of Brain Asymmetries (2016) (2)
Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix (2022) (2)
Genome-wide association study and polygenic risk score analysis for hearing measures in children (2020) (2)
Erratum to: Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions (2000) (2)
In Troyer syndrome Spartin loss induces Complex I impairments and alters pyruvate metabolism (2018) (1)
Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample (2020) (1)
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities (2022) (1)
Reply to Repping et al. (2004) (1)
Genome-wide screening for DNA variants associated with dyslexia and language impairment (2012) (1)
Polygenic risk scores implicate genetic pathways involved in neurodevelopmental disorders in hearing thresholds and hearing asymmetry in children (2020) (1)
Identification of genetic interactions involved in dyslexia pathogenesis (2017) (0)
haracterization of a Family with Rare Deletions in NTNAP5 and DOCK4 Suggests Novel Risk Loci for utism and Dyslexia (0)
Meta-analysis on human footedness (2020) (0)
SA14THE KIAA0319 DYSLEXIA SUSCEPTIBILITY GENE PRESENTS A HIGHLY SPECIFIC EXPRESSION PATTERN DURING ZEBRAFISH DEVELOPMENT AND PLAYS A ROLE IN CYTOSKELETON DYNAMICS (2019) (0)
SA13FUNCTIONAL CHARACTERIZATION OF ATP2C2, A RISK FACTOR FOR LANGUAGE DISORDERS (2019) (0)
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia (2023) (0)
A genome-wide association study of Chinese and English language abilities in Hong Kong Chinese children (2022) (0)
A genome-wide association screen of quantitative reading and language traits in >22,000 people in the GenLang consortium (2019) (0)
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes (2016) (0)
GENOME-WIDE ASSOCIATION STUDY META-ANALYSIS OF SOCIAL ANXIETY DISORDER (2022) (0)
Handedness in twins: meta-analyses (2022) (0)
Expression of the KIAA0319 gene from a haplotype associated with developmental dyslexia (2006) (0)
Language and reading impairments are associated with increased prevalence of non-right-handedness. (2023) (0)
Further evidence that KIAA0319 is associated with developmental dyslexia (2006) (0)
A clinal pattern of human Y chromosome diversity in North Africa (2004) (0)
Handedness in Hong Kong (2019) (0)
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to 1 mitochondrial dysfunction with Complex I impairments and altered pyruvate metabolism 2 3 Running title : SPART and mitochondria in Troyer syndrome (2019) (0)
Light-induced asymmetries in the embryonic retina are mediated by the vascular system and extracellular matrix (2021) (0)
Title The DCDC 2 deletion is not a risk factor for dyslexia (2017) (0)

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