Donna M. McDonald‐McGinn

Also affiliated with University of Pennsylvania

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 3%percentile

1.6Author DataRank

Indexed papers

3in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 3 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs

Human Brain Mapping(2021)10.1002/hbm.25354

Top 18%

1.2DataRank

Top 18%73 citations

Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E. Villalón‐Reina +95 more

Papers

Driven by 34 papers — median percentile 70. 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

N/A

1.4DataRank · unranked

89 citations

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

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from theENIGMAworking groups onCNVs

Human Brain Mapping(2021)10.1002/hbm.25354

Top 18%

1.2DataRank

Top 18%73 citations

Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Daqiang Sun, Julio E. Villalón‐Reina +95 more

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

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

N/A

0.738DataRank · unranked

136 citations

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

N/A

0.533DataRank · 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

N/A

0.477DataRank · unranked

23 citations

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

22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis

Journal of Clinical Medicine(2021)10.3390/jcm10214823

N/A

0.476DataRank · unranked

13 citations

Jelle F. Homans, Tom P. C. Schlösser, Michiel L. Houben, Vincent F. X. Deeney, Terrence B. Crowley +6 more

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

Science(2024)10.1126/science.adl1624

N/A

0.464DataRank · unranked

21 citations

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

Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA Working Groups on CNVs

PsyArXiv (OSF Preprints)(2021)10.31234/osf.io/57erc

Top 43%

0.437DataRank

Top 43%12 citations

Christopher R. K. Ching, Sophia I. Thomopoulos, Dennis van der Meer, Julio E. Villalón‐Reina, Ingrid Agartz +95 more

The role of 22q11.2 deletion syndrome in the relationship between congenital heart disease and scoliosis

The Spine Journal(2020)10.1016/j.spinee.2020.01.006

N/A

0.406DataRank · unranked

14 citations

Steven de Reuver, Tracy Heung, Candice K. Silversides, Erwin Oechslin, Michiel L. Houben +5 more

Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

Human Brain Mapping(2024)10.1002/hbm.26553

N/A

0.385DataRank · unranked

6 citations

Christopher R. K. Ching, Anne S. Bassett, Leila Kushan, Kevin M. Antshel, Thérèse van Amelsvoort +42 more

Tbx1 haploinsufficiency leads to local skull deformity, paraflocculus and flocculus dysplasia, and motor-learning deficit in 22q11.2 deletion syndrome

Nature Communications(2024)10.1038/s41467-024-54837-3

N/A

0.352DataRank · unranked

8 citations

J. Eric Schmitt, Yiran Li, Christopher M. Davenport, Jeffrey Steinberg, Audrey Bonnan +17 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

N/A

0.345DataRank · unranked

9 citations

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

N/A

0.330DataRank · unranked

8 citations

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

Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia

Molecular Psychiatry(2023)10.1038/s41380-023-02009-y

N/A

0.311DataRank · unranked

5 citations

Yingjie Zhao, M. Reza Jabalameli, Nha Nguyen, Joydeep Mitra, Ann Swillen +15 more

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

Genes(2023)10.3390/genes14010169

N/A

0.269DataRank · unranked

5 citations

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

Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States

Genes(2021)10.3390/genes12071030

N/A

0.250DataRank · unranked

4 citations

Fadi I. Musfee, Laura E. Mitchell, Elizabeth Goldmuntz, Hongbo M. Xie, Håkon Håkonarson +7 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

N/A

0.165DataRank · unranked

2 citations

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

Optical mapping in Black genomes: Distinct LCR22 structures and 22q11.2 deletion syndrome mechanisms

Genetics in Medicine(2025)10.1016/j.gim.2025.101614

N/A

0.165DataRank · unranked

2 citations

Oanh Tran, Ryan Lapointe, Arnold Z. Olali, Douglas C. Wallace, Bernice Morrow +4 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

N/A

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

N/A

0DataRank · unranked

12 citations

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

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

UNC Libraries(2020)10.17615/5188-7m66

N/A

0DataRank · unranked

0 citations

Donna M. McDonald‐McGinn, Mauricio Arcos‐Burgos, Lina M. Moreno, Andrew C. Lidral, Michel Bahuau +21 more

Inter-rater reliability of subthreshold psychotic symptoms in individuals with 22q11.2 deletion syndrome

Journal of Neurodevelopmental Disorders(2021)10.1186/s11689-021-09372-3

N/A

0DataRank · unranked

1 citations

Deby Salzer, Carrie E. Bearden, Monica E. Calkins, Wendy R. Kates, Leila Kushan +7 more

Cleft palate morphology, genetic etiology, and risk of mortality in infants with Robin sequence

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62430

N/A

0DataRank · unranked

9 citations

Jonathan A. Perkins, Julia Parish‐Morris, Anne Hing, Maida L. Chen, Christopher M. Cielo︎ +12 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

N/A

0DataRank · unranked

17 citations

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

Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation

Prenatal Diagnosis(2024)10.1002/pd.6566

N/A

0DataRank · unranked

7 citations

Anne S. Bassett, Erik Boot, Bruno Marino, Julie S. Moldenhauer, Sólveig Óskarsdóttir +6 more

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants

medRxiv(2020)10.1101/2020.01.14.20017426

N/A

0DataRank · unranked

14 citations

Joanne Doherty, Richard Anney, Kevin M. Antshel, Carrie E. Bearden, Raphael Bernier +26 more

Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology

Biological Psychiatry Cognitive Neuroscience and Neuroimaging(2025)10.1016/j.bpsc.2025.05.010

N/A

0DataRank · unranked

1 citations

Ida E. Sønderby, George Kirov, Abdel Abdellaoui, Ingrid Agartz, David Ames +95 more

Auditory evoked neuromagnetic response latency is associated with language ability in preschoolers with an elevated likelihood of intellectual or developmental disability

Frontiers in Integrative Neuroscience(2025)10.3389/fnint.2025.1585567

N/A

0DataRank · unranked

0 citations

Lauren M. Young, Mina Kim, Shannon Watson, Victoria Kaufman, Bethany Beal +7 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

N/A

0DataRank · unranked

0 citations

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

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

Genes(2022)10.3390/genes13101800

N/A

0DataRank · unranked

4 citations

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

Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes

UNC Libraries(2020)10.17615/86qc-4989

N/A

0DataRank · unranked

0 citations

Thomas Werge, Anders Vangkilde, Koenraad Devriendt, Carolyn Chow, Carrie E. Bearden +27 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

N/A

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

N/A

0DataRank · unranked

0 citations

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

Donna M. McDonald‐McGinn

Indexed papers

Top data-sharing exemplar

Papers