Geraldine A. McDowell

1.2k total citations
19 papers, 865 citations indexed

About

Geraldine A. McDowell is a scholar working on Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Biochemistry. According to data from OpenAlex, Geraldine A. McDowell has authored 19 papers receiving a total of 865 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 8 papers in Pathology and Forensic Medicine and 7 papers in Biochemistry. Recurrent topics in Geraldine A. McDowell's work include Amino Acid Enzymes and Metabolism (7 papers), Neonatal Health and Biochemistry (7 papers) and Biomedical Research and Pathophysiology (7 papers). Geraldine A. McDowell is often cited by papers focused on Amino Acid Enzymes and Metabolism (7 papers), Neonatal Health and Biochemistry (7 papers) and Biomedical Research and Pathophysiology (7 papers). Geraldine A. McDowell collaborates with scholars based in United States, United Kingdom and Cameroon. Geraldine A. McDowell's co-authors include William A. Gahl, Vorasuk Shotelersuk, Yair Anikster, Glenn E. Palomaki, Isa Bernardini, Jess G. Thoene, Juanru Guo, Robert E. Grier, Arthur R. Brothman and Carolyn Sue Richards and has published in prestigious journals such as Nature Genetics, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Geraldine A. McDowell

19 papers receiving 839 citations

Peers

Countries citing papers authored by Geraldine A. McDowell

Since Specialization

Citations

This map shows the geographic impact of Geraldine A. McDowell'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 Geraldine A. McDowell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Geraldine A. McDowell more than expected).

Fields of papers citing papers by Geraldine A. McDowell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Geraldine A. McDowell. 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 Geraldine A. McDowell. The network helps show where Geraldine A. McDowell may publish in the future.

Co-authorship network of co-authors of Geraldine A. McDowell

This figure shows the co-authorship network connecting the top 25 collaborators of Geraldine A. McDowell. A scholar is included among the top collaborators of Geraldine A. McDowell 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 Geraldine A. McDowell. Geraldine A. McDowell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory 2018 ·Hereditary Cancer in Clinical Practice ·(unknown), (unknown), (unknown), Е. А. Богданова, Wenjie Chen, Daniel S. Lupu, Joshua A. Suhl, Qiandong Zeng, Ute Geigenmüller, (unknown), Patricia M. Okamoto, Geraldine A. McDowell, Melissa A. Hayden, Narasimhan Nagan	15
2	Technical standards and guidelines: Prenatal screening for Down syndrome that includes first-trimester biochemistry and/or ultrasound measurements 2009 ·Genetics in Medicine ·Glenn E. Palomaki, (unknown), Jacob A. Canick, Geraldine A. McDowell, Alan E. Donnenfeld	40
3	Quality assessment of routine nuchal translucency measurements: a North American laboratory perspective 2008 ·Genetics in Medicine ·Glenn E. Palomaki, Louis M. Neveux, Alan E. Donnenfeld, (unknown), Geraldine A. McDowell, Jacob A. Canick, Anne Summers, Geralyn Lambert‐Messerlian, Leonard H. Kellner, Arthur M. Zebelman, James E. Haddow	39
4	Technical standards and guidelines: Prenatal screening for open neural tube defects: This new section on “Prenatal Screening for Open Neural Tube Defects,” together with the new section on “Prenatal Screening for Down Syndrome,” replaces the previous Section H of the American College of Medical Genetics Standards and Guidelines for Clinical Genetics Laboratories 2005 ·Genetics in Medicine ·Linda Bradley, Glenn E. Palomaki, Geraldine A. McDowell	13
5	Technical standards and guidelines: Prenatal screening for Down syndrome: This new section on “Prenatal Screening for Down Syndrome,” together with the new section on “Prenatal Screening for Open Neural Tube Defects,” replaces the previous Section H of the American College of Medical Genetics Standards and Guidelines for Clinical Genetics Laboratories 2005 ·Genetics in Medicine ·Glenn E. Palomaki, Linda Bradley, Geraldine A. McDowell	17
6	Comparison of Fresh Frozen Serum to Proficiency Testing Material in College of American Pathologists Surveys: α-Fetoprotein, Carcinoembryonic Antigen, Human Chorionic Gonadotropin, and Prostate-Specific Antigen 2005 ·Archives of Pathology & Laboratory Medicine ·William E. Schreiber, David B. Endres, Geraldine A. McDowell, Glenn E. Palomaki, Ronald J. Elin, George G. Klee, Edward Wang	21
7	Revised Sections F7.5 (Quantitative Amino Acid Analysis) and F7.6 (Qualitative Amino Acid Analysis): American College of Medical Genetics Standards and Guidelines for Clinical Genetics Laboratories, 2003 2004 ·Genetics in Medicine ·Robert E. Grier, William A. Gahl, Tina M. Cowan, Isa Bernardini, Geraldine A. McDowell, Piero Rinaldo	10
8	The sensitivity of the assessment process in screening mammography 2002 ·The Breast ·Geraldine A. McDowell, (unknown), (unknown), (unknown), W. Simpson	1
9	Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics 2001 ·Genetics in Medicine ·Anne Maddalena, Carolyn Sue Richards, Matthew J. McGinniss, Arthur R. Brothman, Robert J. Desnick, Robert E. Grier, Betsy Hirsch, Peter B. Jacky, Geraldine A. McDowell, Bradley W. Popovich, Michael S. Watson, Daynna J. Wolff	180
10	The Genomic Region Encompassing the Nephropathic Cystinosis Gene (CTNS): Complete Sequencing of a 200-kb Segment and Discovery of a Novel Gene within the Common Cystinosis-Causing Deletion 2000 ·Genome Research ·Jeffrey W. Touchman, Yair Anikster, Nicole Dietrich, Valerie V. Maduro, Geraldine A. McDowell, Vorasuk Shotelersuk, Gerard G. Bouffard, Stephen M. Beckstrom‐Sternberg, William A. Gahl, Eric D. Green	101
11	Ocular Nonnephropathic Cystinosis: Clinical, Biochemical, and Molecular Correlations 2000 ·Pediatric Research ·Yair Anikster, Cynthia Lucero, Juanru Guo, Marjan Huizing, Vorasuk Shotelersuk, Isa Bernardini, Geraldine A. McDowell, Fumino Iwata, Muriel I. Kaiser‐Kupfer, (unknown), Jess G. Thoene, Jerry A. Schneider, William A. Gahl	76
12	Identification and Detection of the Common 65-kb Deletion Breakpoint in the Nephropathic Cystinosis Gene (CTNS) 1999 ·Molecular Genetics and Metabolism ·Yair Anikster, Cynthia Lucero, (unknown), Marjan Huizing, Geraldine A. McDowell, Vorasuk Shotelersuk, E D Green, (unknown)	66
13	Clinical and molecular aspects of nephropathic cystinosis 1998 ·Journal of Molecular Medicine ·Geraldine A. McDowell, Margaret Town, William van’t Hoff, William A. Gahl	19
14	CTNS Mutations in an American-Based Population of Cystinosis Patients 1998 ·The American Journal of Human Genetics ·Vorasuk Shotelersuk, David E. Larson, Yair Anikster, Geraldine A. McDowell, Rosemary Lemons, Isa Bernardini, Juanru Guo, Jess G. Thoene, William A. Gahl	128
15	Fine Mapping of the Cystinosis Gene Using an Integrated Genetic and Physical Map of a Region within Human Chromosome Band 17p13 1996 ·Biochemical and Molecular Medicine ·Geraldine A. McDowell, Takao Isogai, Akira Tanigami, Senator Hazelwood, David H. Ledbetter, Mihael H. Polymeropoulos, Uta Lichter‐Konecki, David Konecki, Margaret Town, William van’t Hoff, Jean Weissenbach, William A. Gahl	19
16	Linkage of the gene for cystinosis to markers on the short arm of chromosome 17 1995 ·Nature Genetics ·Geraldine A. McDowell, William A. Gahl, (unknown), Jerry A. Schneider, Jean Weissenbach, Mihael H. Polymeropoulos, Margaret Town, William van’t Hoff, Martin Farrall, Christopher G. Mathew	71
17	Intrafamilial variability in Hurler syndrome and Sanfilippo syndrome type A: Implications for evaluation of new therapies 1993 ·American Journal of Medical Genetics ·Geraldine A. McDowell, Tina M. Cowan, Miriam G. Blitzer, Carol L. Greene	7
18	The presence of two different infantile Tay-Sachs disease mutations in a Cajun population. 1992 ·PubMed ·Geraldine A. McDowell, Emilie H. Mules, (unknown), (unknown), Miriam G. Blitzer	29
19	Tay-Sachs Disease as a Model for Screening Inborn Errors 1992 ·Clinics in Laboratory Medicine ·Miriam G. Blitzer, Geraldine A. McDowell	13

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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