Irina Astrovskaya

Simons Foundation — United States

Neuroscience · Life Sciences

15h-index2.7kcitations40works0.32yr avg
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Research Topics

Autism Spectrum Disorder Research(11), Genomics and Phylogenetic Studies(10), Gut microbiota and health(8), Genomics and Rare Diseases(8), Genetics and Neurodevelopmental Disorders(8)

Publications38 total

Return of genetic research results in 21,532 individuals with autism
Genetics in Medicine·2024· 1 citedOpen Access
P187: Consent frequency for genetic participation and receiving genetic results in White and non-White participants in SPARK
Genetics in Medicine Open·2024Open Access
P199: Frequency of secondary findings and returning these results by self-reported race/ethnicity in SPARK
Genetics in Medicine Open·2024Open Access
P111: Phenotypic insights into newly established moderate effect genes for autism spectrum disorder
Genetics in Medicine Open·2023Open Access
P057: Characteristics of participants who opt to receive secondary findings in SPARK
Genetics in Medicine Open·2023Open Access
Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders
Proceedings of the National Academy of Sciences·2022· 64 citedOpen Access
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Nature Genetics·2022· 423 citedOpen Access
Inferring Genomic Sequences
Digital Archive @ GSU·2022· 2 citedOpen Access
eP287: Return of individual genetic results in the largest recontactable cohort of individuals with autism
Genetics in Medicine·2022· 1 citedOpen Access
eP121: Integrating de novo and inherited variants in over 42,607 autism cases identifies variants in new moderate risk genes
Genetics in Medicine·2022· 3 citedOpen Access
Integrating <i>de novo</i> and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes
2021· 7 citedOpen Access
Recent ultra-rare inherited variants implicate new autism candidate risk genes
Nature Genetics·2021· 137 citedOpen Access
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
Genome Medicine·2021· 108 citedOpen Access
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
Nature Communications·2020· 8 citedOpen Access
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
Nature Communications·2020· 206 citedOpen Access
Beliefs in vaccine as causes of autism among SPARK cohort caregivers
Vaccine·2020· 33 citedOpen Access
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes
npj Genomic Medicine·2019· 264 citedOpen Access
Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes
2019· 5 citedOpen Access
Individual-specific changes in the human gut microbiota after challenge with enterotoxigenic Escherichia coli and subsequent ciprofloxacin treatment
BMC Genomics·2016· 62 citedOpen Access
Additional file 4: of Individual-specific changes in the human gut microbiota after challenge with enterotoxigenic Escherichia coli and subsequent ciprofloxacin treatment
Figshare·2016Open Access
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Frequent Co-authors

Pamela Feliciano(17), Natalia Volfovsky(13), Mihai Pop(12), Wendy K. Chung(11), Xueya Zhou(10), LeeAnne Green Snyder(10), Jacob B. Hall(9), Leo Brueggeman(9), Tychele N. Turner(9), Yufeng Shen(9), Tianyun Wang(8), Alpha Amatya(8), Asif Bashar(8), Evan E. Eichler(8), Brian J. O’Roak(7), Alexandra Goler(7), J. Andrea(7), John Acampado(7), Elizabeth Brooks(7), Jacob J. Michaelson(7)