Deborah A. Driscoll

11.5k total citations · 1 hit paper
102 papers, 7.3k citations indexed

About

Deborah A. Driscoll is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Epidemiology. According to data from OpenAlex, Deborah A. Driscoll has authored 102 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 39 papers in Pulmonary and Respiratory Medicine and 34 papers in Epidemiology. Recurrent topics in Deborah A. Driscoll's work include Congenital heart defects research (54 papers), Congenital Heart Disease Studies (32 papers) and Tracheal and airway disorders (26 papers). Deborah A. Driscoll is often cited by papers focused on Congenital heart defects research (54 papers), Congenital Heart Disease Studies (32 papers) and Tracheal and airway disorders (26 papers). Deborah A. Driscoll collaborates with scholars based in United States, Germany and Poland. Deborah A. Driscoll's co-authors include Elaine H. Zackai, Donna M. McDonald‐McGinn, Beverly S. Emanuel, Andrea Dunaif, Richard S. Legro, Marcia L. Budarf, Jerome F. Strauss, Elizabeth Goldmuntz, Janis H. Fox and Susan J. Gross and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Deborah A. Driscoll

101 papers receiving 7.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Evidence for a genetic basis for hyperandrogenemia in polycystic ovary syndrome

1998 526 citations Deborah A. Driscoll et al. profile →

Peers

Deborah A. Driscoll

MB

GENET

EPIDE

PRM

RM

David Chitayat Canada

Raja Brauner France

Michael A. Rosenberg United States

M Massobrio Italy

Constance A. Griffin United States

Filiberto Maria Severi Italy

Monica Miozzo Italy

Marc De Braekeleer France

Martin O. Savage United Kingdom

Eleanor Feingold United States

David Chitayat Canada

Deborah A. Driscoll

4.8k ×1.2

MB

3.3k ×1.4

GENET

823 ×0.4

EPIDE

867 ×0.4

PRM

208 ×0.2

RM

Citations per year, relative to Deborah A. Driscoll Deborah A. Driscoll (= 1×) peers David Chitayat

Countries citing papers authored by Deborah A. Driscoll

Since Specialization

Citations

This map shows the geographic impact of Deborah A. Driscoll's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Deborah A. Driscoll with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deborah A. Driscoll more than expected).

Fields of papers citing papers by Deborah A. Driscoll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah A. Driscoll. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Deborah A. Driscoll. The network helps show where Deborah A. Driscoll may publish in the future.

Co-authorship network of co-authors of Deborah A. Driscoll

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah A. Driscoll. A scholar is included among the top collaborators of Deborah A. Driscoll based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Deborah A. Driscoll. Deborah A. Driscoll is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Friedman, Lisa S., Kimberly Schadt, Karlla W. Brigatti, et al.. (2010). Pregnancy with Friedreich ataxia: a retrospective review of medical risks and psychosocial implications. American Journal of Obstetrics and Gynecology. 203(3). 224.e1–224.e5. 6 indexed citations

2.

Busse, Tracy, John M. Graham, Gerald L. Feldman, et al.. (2010). High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome. Human Mutation. 32(1). 91–97. 15 indexed citations

3.

Driscoll, Deborah A. & Susan J. Gross. (2009). Prenatal Screening for Aneuploidy. New England Journal of Medicine. 360(24). 2556–2562. 123 indexed citations

4.

Sundaram, Usha, Donna M. McDonald‐McGinn, Dale S. Huff, et al.. (2007). Primary amenorrhea and absent uterus in the 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 143A(17). 2016–2018. 32 indexed citations

5.

Sherman, Stephanie L., Beth A. Pletcher, & Deborah A. Driscoll. (2005). Fragile X syndrome: Diagnostic and carrier testing. Genetics in Medicine. 7(8). 584–587. 202 indexed citations

6.

Odibo, Anthony, et al.. (2003). Screening for Aneuploidy in Twin Pregnancies: Maternal Age- and Race-specific Risk Assessment Between 9–14 Weeks. Twin Research. 6(4). 251–256. 6 indexed citations

7.

Odibo, Anthony, et al.. (2003). Screening for Aneuploidy in Twin Pregnancies: Maternal Age- and Race-specific Risk Assessment Between 9–14 Weeks. Twin Research. 6(4). 251–256. 1 indexed citations

8.

Saitta, Sulagna C., Deborah A. Driscoll, Donna M. McDonald‐McGinn, et al.. (2003). Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion. Human Molecular Genetics. 13(4). 417–428. 109 indexed citations

9.

Gracia, Clarisa R. & Deborah A. Driscoll. (2003). Molecular basis of pubertal abnormalities. Obstetrics and Gynecology Clinics of North America. 30(2). 261–277. 3 indexed citations

10.

Driscoll, Deborah A.. (2001). Prenatal diagnosis of the 22q11.2 deletion syndrome. Genetics in Medicine. 3(1). 14–18. 43 indexed citations

11.

Gerdes, Marsha, Cynthia Solot, Paul P. Wang, et al.. (1999). Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion. American Journal of Medical Genetics. 85(2). 127–133. 10 indexed citations

12.

Goldmuntz, Elizabeth, Bernard J. Clark, Laura E. Mitchell, et al.. (1998). Frequency of 22q11 deletions in patients with conotruncal defects. Journal of the American College of Cardiology. 32(2). 492–498. 373 indexed citations

13.

Driscoll, Deborah A., et al.. (1997). PCR Assay for Screening Patients At Risk for 22q11.2 Deletion. Genetic Testing. 1(2). 109–113. 18 indexed citations

14.

Kiriakidou, Marianthi, Deborah A. Driscoll, Jesús M. López-Guisa, & Jerome F. Strauss. (1997). Cloning and Expression of Primate Daxx cDNAs and Mapping of the Human Gene to Chromosome 6p21.3 in the MHC Region. DNA and Cell Biology. 16(11). 1289–1298. 50 indexed citations

15.

Gǒng, Wànkuí, Beverly S. Emanuel, Naomi Galili, et al.. (1997). Structural and Mutational Analysis of a Conserved Gene (DGSI) from the Minimal DiGeorge Syndrome Critical Region. Human Molecular Genetics. 6(2). 267–276. 36 indexed citations

16.

Budarf, Marcia L., Barbara Eckman, Dominique Michaud, et al.. (1996). Regional Localization of over 300 Loci on Human Chromosome 22 Using a Somatic Cell Hybrid Mapping Panel. Genomics. 35(2). 275–288. 24 indexed citations

17.

Driscoll, Deborah A. & Beverly S. Emanuel. (1996). DiGeorge and velocardiofacial syndromes: The 22q11 deletion syndrome. Mental Retardation and Developmental Disabilities Research Reviews. 2(3). 130–138. 12 indexed citations

18.

Junker, Anne & Deborah A. Driscoll. (1995). Humoral immunity in DiGeorge syndrome. The Journal of Pediatrics. 127(2). 231–237. 61 indexed citations

19.

Driscoll, Deborah A., Beverly S. Emanuel, & Elizabeth Goldmuntz. (1994). Velopharyngeal incompetence diagnosed in a series of cardiac patients prompted by the finding of a 22q11.2 deletion. The American Journal of Human Genetics. 55. 5 indexed citations

20.

Driscoll, Deborah A.. (1994). Genetic basis of DiGeorge and velocardiofacial syndromes. Current Opinion in Pediatrics. 6(6). 702–706. 38 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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