Donna M. McDonald-McGinn

ScholarGPS® ID: 61395752583630

Affiliation
Children's Hospital of Philadelphia
Affiliation History

Field
Life Sciences
Discipline
Genetics
Top Specialties
Chromosomal Deletion Syndrome | Medical Genetics | Chromosome | Birth Defect | Mutation | Congenital Heart Defect | Molecular Genetics | Schizophrenia | Thorax | Autism | Biological Psychiatry | Cardiac Surgery | Human Genetics | Plastic Surgery | Psychosis
Metrics Summary
Publication Count
343
Predicted Citations
24,808
Predicted h-index
83
Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

  • Publications
  • Books
  • Patents
  • NIH/NSF
You must register and claim your profile to add or remove publications from it.
... publications
FILTER BY:
Year
Type
Specialty
Affiliations
Access
Co-Authors
Add
Delete
The mental health and traumatic experiences of mothers of children with 22q11DS (journal article)
Finless, Alexandra | Rideout, Andrea L. | Xiong, Ting | Carbyn, Holly | Lingley-Pottie, Patricia | Palmer, Lisa D. | Shugar, Andrea | McDonald-McGinn, Donna M. | McGrath, Patrick J. | Bassett, Anne S. | ... | Meier, Sandra
European Journal of Psychotraumatology, volume 15, issue 1 (2024).
10.1080/20008066.2024.2353532
Cited by (1) | Cite | Source
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgery (journal article)
Crowley, T. Blaine | Campbell, Ian | Arulselvan, Abinaya | Friedman, David | Zackai, Elaine H. | Geoffrion, Tracy R. | Witmer, Char | Gaynor, J. William | McDonald-McGinn, Donna M. | Lambert, Michele P.
Platelets, volume 35, issue 1 (2024).
10.1080/09537104.2023.2290108
Cite | Source
The clinical course of individuals with 22q11.2 deletion syndrome converting to psychotic disorders: a long-term retrospective follow-up (journal article)
Kulikova, Katerina | Schneider, Maude | McDonald McGinn, Donna M. | Dar, Shira | Taler, Michal | Schwartz-Lifshitz, Maya | Eliez, Stephan | Gur, Raquel E. | Gothelf, Doron
European Child & Adolescent Psychiatry (2024).
10.1007/s00787-024-02469-9
Cite | Source
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation (journal article)
Goldmuntz, Elizabeth | Bassett, Anne S. | Boot, Erik | Marino, Bruno | Moldenhauer, Julie S. | Óskarsdóttir, Sólveig | Putotto, Carolina | Rychik, Jack | Schindewolf, Erica | McDonald‐McGinn, Donna M. | Blagowidow, Natalie
Prenatal Diagnosis, volume 44, issue 6-7, pages 804-814 (2024).
10.1002/pd.6566
Cited by (1) | Cite | Source
Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome (journal article)
Gaiser, Kimberly B. | Schindewolf, Erica M. | Conway, Laura J. | Coleman, Beverly G. | Oliver, Edward R. | Rychik, Jack R. | Debari, Suzanne E. | Mcdonald‐Mcginn, Donna M. | Zackai, Elaine H. | Moldenhauer, Julie S. | Gebb, Juliana S.
Prenatal Diagnosis, volume 44, issue 6-7, pages 796-803 (2024).
10.1002/pd.6555
Cited by (1) | Cite | Source
Remote assessment of the Penn computerised neurocognitive battery in individuals with 22q11.2 deletion syndrome (journal article)
White, L. K. | Hillman, N. | Ruparel, K. | Moore, T. M. | Gallagher, R. S. | McClellan, E. J. | Roalf, D. R. | Scott, J. C. | Calkins, M. E. | McGinn, D. E. | ... | Gur, R. C.
Journal of Intellectual Disability Research, volume 68, issue 4, pages 369-376 (2024).
10.1111/jir.13115
Cited by (1) | Cite | Source
Inflammatory Proteomic Analysis of 22q11.2 Deletion Syndrome (journal article)
Frusone, Valentina | Maurer, Kelly | Emanuel, Beverly S. | McDonald-McGinn, Donna | Sullivan, Kathleen E.
Journal of Clinical Immunology, volume 44, issue 3 (2024).
10.1007/s10875-024-01689-7
Cite | Source
Hematologic and Immunologic Cases: Recurrent Infections in Childhood (book chapter)
In Genomics in the Clinic
Barry, Jessica C. | McDonald-McGinn, Donna M.
Elsevier (2024)
10.1016/B978-0-12-816478-5.00063-7
Cite | Source
P217: Abnormalities of TBX1 result in broad overlapping features of 22q11.2 deletion syndrome (journal article)
McDonald-McGinn, Donna | Giunta, Victoria | Crowley, T. Blaine | McGinn, Daniel | Rockart, Lydia | Green, Audrey | Emanuel, Beverly | Smith, Rosemarie | Moran, Ellen | Geremek, Maciej | ... | Nowakowska, Beata
Genetics in Medicine Open, volume 2 (2024).
10.1016/j.gimo.2024.101114
Cite | Source
P386: Agenesis of olfactory apparatus due to intragenic deletion of SIN3A and MAN2C1 resulting in Witteveen-Kolk syndrome (journal article)
Donoghue, Sarah | Skraban, Cara | Squicciarini, Jake | Wang, Jing | Rippert, Alyssa | McDonald-McGinn, Donna | Zackai, Elaine
Genetics in Medicine Open, volume 2 (2024).
10.1016/j.gimo.2024.101280
Cite | Source
Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome (journal article)
Gur, Raquel E. | McDonald-McGinn, Donna M. | Moore, Tyler M. | Gallagher, R. Sean | McClellan, Emily | White, Lauren | Ruparel, Kosha | Hillman, Noah | Crowley, T. Blaine | McGinn, Daniel E. | ... | Gur, Ruben C.
Psychological Medicine, volume 53, issue 14, pages 6763-6772 (2023).
10.1017/S0033291723000259
Cited by (2) | Cite | Source
An online survey to understand the needs of caregivers of family members with 22q11 deletion syndrome (journal article)
Cosman, T. | Finless, A. | Rideout, A. L. | Lingley‐Pottie, P. | Palmer, L. D. | Shugar, A. | McDonald‐McGinn, D. M. | Swillen, A. | McGrath, P. J. | Bassett, A. S. | ... | Meier, S.
Journal of Intellectual Disability Research, volume 67, issue 9, pages 860-868 (2023).
10.1111/jir.13061
Cite | Source
Approaches to studying the impact of 22q11.2 copy number variants (journal article)
Bassett, Anne S. | McDonald-McGinn, Donna M. | Boot, Erik | Óskarsdóttir, Sólveig | Yuen, Ryan K.C.
The American Journal of Human Genetics, volume 110, issue 7, pages 1216-1218 (2023).
10.1016/j.ajhg.2023.05.008
Cited by (2) | Cite | Source
Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications (journal article)
Bhattarai, Dharmagat | McGinn, Daniel E. | Crowley, T. Blaine | Giunta, Victoria | Gaiser, Kimberly | Zackai, Elaine H. | Emanuel, Beverly S. | Heimall, Jennifer | Jyonouchi, Soma | Lee, Juhee | ... | Sullivan, Kathleen E.
Journal of Clinical Immunology, volume 43, issue 4, pages 794-807 (2023).
10.1007/s10875-023-01443-5
Cited by (4) | Cite | Source
A step closer to understanding the predisposition to autoimmunity as well humoral defects in aging patients with 22q11.2 deletion syndrome (journal article)
Alsaati, Nouf | Maurer, Kelly | McDonald-McGinn, Donna | Sullivan, Kathleen
Clinical Immunology, volume 250 (2023).
10.1016/j.clim.2023.109493
Cite | Source
Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants (journal article)
Verbesselt, Jente | Solot, Cynthia B. | Van Den Heuvel, Ellen | Crowley, T. Blaine | Giunta, Victoria | Breckpot, Jeroen | McDonald-McGinn, Donna M. | Zink, Inge | Swillen, Ann
Genes, volume 14, issue 3, pages 679- (2023).
10.3390/genes14030679
Cited by (3) | Cite | Source
Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome (journal article)
Gaiser, Kimberly B. | Schindewolf, Erica M. | Moldenhauer, Julie S. | Coleman, Beverly G. | Oliver, Edward R. | Rychik, Jack R. | McDonald-McGinn, Donna | Gebb, Juliana S.
American Journal of Obstetrics and Gynecology, volume 228, issue 1, pages S502-S503 (2023).
10.1016/j.ajog.2022.11.861
Cite | Source
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions (journal article)
Blagowidow, Natalie | Nowakowska, Beata | Schindewolf, Erica | Grati, Francesca Romana | Putotto, Carolina | Breckpot, Jeroen | Swillen, Ann | Crowley, Terrence Blaine | Loo, Joanne C. Y. | Lairson, Lauren A. | ... | McDonald-McGinn, Donna M.
Genes, volume 14, issue 1, pages 160- (2023).
10.3390/genes14010160
Cited by (13) | Cite | Source
Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression (journal article)
Campbell, Ian M. | Crowley, T. Blaine | Jobaliya, Chintan | Bailey, Alice | McGinn, Daniel E. | Gaiser, Kimberly | Bassett, Anne | Gur, Raquel E. | Morrow, Bernice | Emanuel, Beverly S. | ... | Lambert, Michele P.
Clinical Genetics, volume 103, issue 1, pages 109-113 (2023).
10.1111/cge.14227
Cited by (2) | Cite | Source
Chromosome 22q11 copy number variants and single ventricle CHD (journal article)
Geoffrion, Tracy R. | Goldberg, David | Crowley, T. Blaine | Chen, Jonathan M. | McDonald-McGinn, Donna M. | Gaynor, J. William
Cardiology in the Young, volume 33, issue 1, pages 101-105 (2023).
10.1017/S1047951122000385
Cite | Source