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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Pregnancy with Friedreich ataxia: a retrospective review of medical risks and psychosocial implications 2010 ·American Journal of Obstetrics and Gynecology ·Lisa S. Friedman, (unknown), Kimberly Schadt, Karlla W. Brigatti, Deborah A. Driscoll, Jennifer Farmer, David R. Lynch	6
2	High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome 2010 ·Human Mutation ·Tracy Busse, John M. Graham, Gerald L. Feldman, Juan C. Perín, (unknown), Robert C. Knowlton, Eric Rappaport, Beverly S. Emanuel, Deborah A. Driscoll, Sulagna C. Saitta	15
3	Prenatal Screening for Aneuploidy 2009 ·New England Journal of Medicine ·Deborah A. Driscoll, Susan J. Gross	123
4	Primary amenorrhea and absent uterus in the 22q11.2 deletion syndrome 2007 ·American Journal of Medical Genetics Part A ·Usha Sundaram, Donna M. McDonald‐McGinn, Dale S. Huff, Beverly S. Emanuel, Elaine H. Zackai, Deborah A. Driscoll, Joann Bodurtha	32
5	Fragile X syndrome: Diagnostic and carrier testing 2005 ·Genetics in Medicine ·Stephanie L. Sherman, Beth A. Pletcher, Deborah A. Driscoll	202
6	Screening for Aneuploidy in Twin Pregnancies: Maternal Age- and Race-specific Risk Assessment Between 9–14 Weeks 2003 ·Twin Research ·Anthony Odibo, (unknown), Serdar Ural, Deborah A. Driscoll, Michael T. Mennuti, George A. Macones	6
7	Screening for Aneuploidy in Twin Pregnancies: Maternal Age- and Race-specific Risk Assessment Between 9–14 Weeks 2003 ·Twin Research ·Anthony Odibo, (unknown), Serdar Ural, Deborah A. Driscoll, Michael T. Mennuti, George A. Macones	1
8	Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion 2003 ·Human Molecular Genetics ·Sulagna C. Saitta, (unknown), (unknown), Deborah A. Driscoll, Donna M. McDonald‐McGinn, Melissa Maisenbacher, (unknown), Prabir K. Chakraborty, April M. Hacker, Elaine H. Zackai, Terry Ashley, Beverly S. Emanuel	109
9	Molecular basis of pubertal abnormalities 2003 ·Obstetrics and Gynecology Clinics of North America ·Clarisa R. Gracia, Deborah A. Driscoll	3
10	Prenatal diagnosis of the 22q11.2 deletion syndrome 2001 ·Genetics in Medicine ·Deborah A. Driscoll	43
11	Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion 1999 ·American Journal of Medical Genetics ·Marsha Gerdes, Cynthia Solot, Paul P. Wang, Edward Moss, Don LaRossa, Peter Randall, Elizabeth Goldmuntz, Bernard J. Clark, Deborah A. Driscoll, Abbas F. Jawad, Beverly S. Emanuel, Donna M. McDonald‐McGinn, Mark L. Batshaw, Elaine H. Zackai	10
12	Frequency of 22q11 deletions in patients with conotruncal defects 1998 ·Journal of the American College of Cardiology ·Elizabeth Goldmuntz, Bernard J. Clark, Laura E. Mitchell, Abbas F. Jawad, Bettina F. Cuneo, Lori A. Reed, Donna M. McDonald‐McGinn, (unknown), (unknown), Elaine H. Zackai, Beverly S. Emanuel, Deborah A. Driscoll	373
13	PCR Assay for Screening Patients At Risk for 22q11.2 Deletion 1997 ·Genetic Testing ·Deborah A. Driscoll, Beverly S. Emanuel, (unknown), Marcia L. Budarf	18
14	Cloning and Expression of Primate Daxx cDNAs and Mapping of the Human Gene to Chromosome 6p21.3 in the MHC Region 1997 ·DNA and Cell Biology ·Marianthi Kiriakidou, Deborah A. Driscoll, Jesús M. López-Guisa, Jerome F. Strauss	50
15	Structural and Mutational Analysis of a Conserved Gene (DGSI) from the Minimal DiGeorge Syndrome Critical Region 1997 ·Human Molecular Genetics ·Wànkuí Gǒng, Beverly S. Emanuel, Naomi Galili, David H. Kim, B.A. Roe, Deborah A. Driscoll, Marcia L. Budarf	36
16	Regional Localization of over 300 Loci on Human Chromosome 22 Using a Somatic Cell Hybrid Mapping Panel 1996 ·Genomics ·Marcia L. Budarf, Barbara Eckman, Dominique Michaud, Terrence P. McDonald, (unknown), Kenneth H. Buetow, (unknown), (unknown), Catherine Hilliard, Deborah A. Driscoll, Elizabeth Goldmuntz, Eckart Meese, Ellen C. Zwarthoff, Sloan R. Williams, Heather E. McDermid, Jan P. Dumanski, Jaclyn A. Biegel, Callum J. Bell, Beverly S. Emanuel	24
17	DiGeorge and velocardiofacial syndromes: The 22q11 deletion syndrome 1996 ·Mental Retardation and Developmental Disabilities Research Reviews ·Deborah A. Driscoll, Beverly S. Emanuel	12
18	Humoral immunity in DiGeorge syndrome 1995 ·The Journal of Pediatrics ·Anne Junker, Deborah A. Driscoll	61
19	Velopharyngeal incompetence diagnosed in a series of cardiac patients prompted by the finding of a 22q11.2 deletion 1994 ·The American Journal of Human Genetics ·Deborah A. Driscoll, Beverly S. Emanuel, Elizabeth Goldmuntz	5
20	Genetic basis of DiGeorge and velocardiofacial syndromes 1994 ·Current Opinion in Pediatrics ·Deborah A. Driscoll	38

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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