T. Blaine Crowley

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 18 papers. Top paper: “Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness”.

Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness

American Journal of Psychiatry(2020)10.1176/appi.ajp.2019.19060583

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1.4DataRank · unranked

89 citations

Boris A. Gutman, Daqiang Sun, Julio E. Villalón‐Reina, Anjanibhargavi Ragothaman, Dmitry Isaev +50 more

Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR)

Scientific Reports(2020)10.1038/s41598-020-69134-4

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0DataRank · unranked

34 citations

Oanh Tran, Andrea Jin, Danielle Carrado, Benjamin A. Silva, Lahari Uppuluri +13 more

Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.06.007

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0DataRank · unranked

23 citations

Ian M. Campbell, Emily J. Liebling, Michele P. Lambert, Lorraine E. Levitt Katz, Jennifer Heimall +5 more

A Comprehensive Analysis of Cerebellar Volumes in the 22q11.2 Deletion Syndrome

Biological Psychiatry Cognitive Neuroscience and Neuroimaging(2021)10.1016/j.bpsc.2021.11.008

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0DataRank · unranked

17 citations

John J. DeBevits, David R. Roalf, Kosha Ruparel, Robert S. Gallagher, Ruben C. Gur +12 more

Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression

Clinical Genetics(2022)10.1111/cge.14227

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0DataRank · unranked

9 citations

T. Blaine Crowley, Chintan Jobaliya, Alice Bailey, Daniel E. McGinn, Kimberly Gaiser +10 more

Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome

Genes(2022)10.3390/genes13101800

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0DataRank · unranked

4 citations

T. Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H. Zackai +7 more

A Novel Non-Allelic Homologous Recombination Event in a Parent with an 11;22 Reciprocal Translocation Leading to 22q11.2 Deletion Syndrome

Genes(2022)10.3390/genes13091668

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0DataRank · unranked

1 citations

Oanh Tran, Daniel E. McGinn, T. Blaine Crowley, Elaine H. Zackai, Donna M. McDonald‐McGinn +2 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.30.507111

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0DataRank · unranked

0 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +45 more

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age

American Journal of Obstetrics and Gynecology(2023)10.1016/j.ajog.2023.09.005

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0DataRank · unranked

15 citations

Stephanie Galloway, T. Blaine Crowley, Julie S. Moldenhauer, Ann Swillen, Jeroen Breckpot +57 more

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS

npj Genomic Medicine(2023)10.1038/s41525-023-00363-y

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0DataRank · unranked

12 citations

Yujue Wang, Lijie Shi, Donna M. McDonald‐McGinn, T. Blaine Crowley, Daniel E. McGinn +47 more

Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63385

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0DataRank · unranked

7 citations

Lydia S. Williams, Niambi Brewer, Lea F. Surrey, Abhay Srinivasan, Dong Li +14 more

Gathering the Stakeholder’s Perspective: Experiences and Opportunities in Rare Genetic Disease Research

Genes(2023)10.3390/genes14010169

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0DataRank · unranked

5 citations

T. Blaine Crowley, Brenda Finucane, Emily McClellan, Sarah Donoghue, Sixto García‐Miñáur +10 more

Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications

Journal of Clinical Immunology(2023)10.1007/s10875-023-01443-5

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0DataRank · unranked

8 citations

Daniel E. McGinn, T. Blaine Crowley, Victoria Giunta, Kimberly Gaiser, Elaine H. Zackai +8 more

Risk of meningomyelocele mediated by the common 22q11.2 deletion

Science(2024)10.1126/science.adl1624

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0DataRank · unranked

21 citations

Sangmoon Lee, Kit Sing Au, T. Blaine Crowley, Valeria Capra, Meade Haller +74 more

ZNF280A links DNA double-strand break repair to human 22q11.2 distal deletion syndrome

Nature Cell Biology(2025)10.1038/s41556-025-01674-1

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0DataRank · unranked

2 citations

Hyo Min Cho, Ilaria Ceppi, Boya Gao, Tribhuwan Yadav, Giórgia Gobbi da Silveira +22 more

Prevalence and spectrum of congenital heart disease in individuals with distal chromosome 22q11.22-23 deletions

medRxiv(2025)10.1101/2025.10.15.25337915

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0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 more

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Molecular Psychiatry(2020)10.1038/s41380-020-0654-3

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0DataRank · unranked

136 citations

Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston +95 more

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics(2025)10.1111/cge.70118

N/A

0DataRank · unranked

0 citations

Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta +18 more