Fred Lorey

5.2k total citations
78 papers, 2.9k citations indexed

About

Fred Lorey is a scholar working on Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Genetics. According to data from OpenAlex, Fred Lorey has authored 78 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Pediatrics, Perinatology and Child Health, 26 papers in Clinical Biochemistry and 19 papers in Genetics. Recurrent topics in Fred Lorey's work include Neonatal Health and Biochemistry (28 papers), Metabolism and Genetic Disorders (26 papers) and Hemoglobinopathies and Related Disorders (19 papers). Fred Lorey is often cited by papers focused on Neonatal Health and Biochemistry (28 papers), Metabolism and Genetic Disorders (26 papers) and Hemoglobinopathies and Related Disorders (19 papers). Fred Lorey collaborates with scholars based in United States, Canada and Australia. Fred Lorey's co-authors include George C. Cunningham, Robert J. Currier, Elliott Vichinsky, Lisa Feuchtbaum, John Sherwin, G C Cunningham, Bertram H. Lubin, George Cunningham, John S. Waye and Kenneth A. Pass and has published in prestigious journals such as PEDIATRICS, American Journal of Epidemiology and Environmental Health Perspectives.

In The Last Decade

Fred Lorey

78 papers receiving 2.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Fred Lorey United States 31 1.1k 776 717 693 629 78 2.9k
Bradford L. Therrell United States 31 1.3k 1.2× 1.0k 1.3× 579 0.8× 1.3k 1.9× 505 0.8× 103 3.4k
Michele A. Lloyd-Puryear United States 27 918 0.8× 677 0.9× 509 0.7× 974 1.4× 336 0.5× 72 2.9k
Michele Caggana United States 31 477 0.4× 1.1k 1.5× 404 0.6× 463 0.7× 264 0.4× 135 3.3k
Carmencita D. Padilla Philippines 22 962 0.9× 449 0.6× 371 0.5× 570 0.8× 141 0.2× 115 2.2k
G. M. Addison United Kingdom 24 471 0.4× 548 0.7× 288 0.4× 176 0.3× 617 1.0× 62 2.5k
Kenneth A. Pass United States 24 523 0.5× 459 0.6× 115 0.2× 337 0.5× 179 0.3× 68 2.0k
Michael T. Geraghty United States 36 402 0.4× 1.9k 2.4× 159 0.2× 913 1.3× 121 0.2× 121 3.6k
N. Saha Singapore 25 169 0.2× 642 0.8× 200 0.3× 191 0.3× 219 0.3× 91 3.3k
George R. Honig United States 25 391 0.4× 1.1k 1.4× 839 1.2× 76 0.1× 659 1.0× 91 2.6k
Pranesh Chakraborty Canada 27 545 0.5× 802 1.0× 140 0.2× 511 0.7× 59 0.1× 100 2.0k

Countries citing papers authored by Fred Lorey

Since Specialization
Citations

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

Fields of papers citing papers by Fred Lorey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fred Lorey. 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 Fred Lorey. The network helps show where Fred Lorey may publish in the future.

Co-authorship network of co-authors of Fred Lorey

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

All Works

20 of 20 papers shown
1.
Gallant, Natalie M., Yael Wilnai, Fred Lorey, et al.. (2017). Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California. Molecular Genetics and Metabolism. 122(3). 76–84. 20 indexed citations
2.
Hodgkinson, C. Paul, Sylvia B. Smith, Fred Lorey, et al.. (2014). ПРЕНАТАЛЬНЫЙ СКРИНИНГ ХРОМОСОМНЫХ АНОМАЛИЙ С ИСПОЛЬЗОВАНИЕМ ТРОЙНОГО МАРКЕРА. Reproductive Endocrinology. 84–90. 1 indexed citations
3.
Lawrence, Roger, Jillian R. Brown, Fred Lorey, et al.. (2013). Glycan-based biomarkers for mucopolysaccharidoses. Molecular Genetics and Metabolism. 111(2). 73–83. 57 indexed citations
4.
Lin, Henry J., et al.. (2011). Extremely high phenylalanine levels in a newborn on parenteral nutrition: phenylketonuria in the neonatal intensive care unit. Journal of Perinatology. 31(7). 507–510. 10 indexed citations
5.
Feuchtbaum, Lisa, et al.. (2010). The context and approach for the California newborn screening short- and long-term follow-up data system: Preliminary findings. Genetics in Medicine. 12(12 Suppl). S242–S250. 22 indexed citations
6.
Tortorelli, Silvia, Coleman Turgeon, José E. Abdenur, et al.. (2010). Two-Tier Approach to the Newborn Screening of Methylenetetrahydrofolate Reductase Deficiency and Other Remethylation Disorders with Tandem Mass Spectrometry. The Journal of Pediatrics. 157(2). 271–275. 25 indexed citations
7.
Hubbard, Walter C., Ann B. Moser, Richard O. Jones, et al.. (2009). Newborn screening for X-linked adrenoleukodystrophy (X-ALD): Validation of a combined liquid chromatography–tandem mass spectrometric (LC–MS/MS) method. Molecular Genetics and Metabolism. 97(3). 212–220. 124 indexed citations
8.
Buffler, Patricia A., Michael A. Kelsh, Edmund Lau, et al.. (2005). Thyroid Function and Perchlorate in Drinking Water: An Evaluation among California Newborns, 1998. Environmental Health Perspectives. 114(5). 798–804. 21 indexed citations
9.
Crawford, Dana C., Michele Caggana, Katharine B. Harris, et al.. (2002). Characterization of β-globin haplotypes using blood spots from a population-based cohort of newborns with homozygous HbS. Genetics in Medicine. 4(5). 328–335. 12 indexed citations
10.
Lorey, Fred, George Cunningham, Elliott Vichinsky, et al.. (2001). Universal Newborn Screening for Hb H Disease in California. Genetic Testing. 5(2). 93–100. 78 indexed citations
11.
Lorey, Fred, Pimlak Charoenkwan, H. Ewa Witkowska, et al.. (2001). Hb H hydrops foetalis syndrome: a case report and review of literature. British Journal of Haematology. 115(1). 72–78. 65 indexed citations
12.
Reed, William, et al.. (2000). Sickle-cell disease not identified by newborn screening because of prior transfusion. The Journal of Pediatrics. 136(2). 248–250. 15 indexed citations
13.
Lorey, Fred. (2000). Asian Immigration and Public Health in California: Thalassemia in Newborns in California. ˜The œAmerican journal of pediatric hematology/oncology. 22(6). 564–566. 35 indexed citations
14.
Feuchtbaum, Lisa, Robert J. Currier, Fred Lorey, & George C. Cunningham. (2000). Prenatal ultrasound findings in affected and unaffected pregnancies that are screen-positive for trisomy 18: the California experience. Prenatal Diagnosis. 20(4). 293–299. 17 indexed citations
15.
Feuchtbaum, Lisa, et al.. (1999). Neural Tube Defect Prevalence in California (1990-1994): Eliciting Patterns by Type of Defect and Maternal Race/Ethnicity. Genetic Testing. 3(3). 265–272. 72 indexed citations
16.
Lorey, Fred & George Cunningham. (1998). Impact of Asian Immigration on Thalassemia in California. Annals of the New York Academy of Sciences. 850(1). 442–445. 8 indexed citations
17.
Hiti, Alan L., et al.. (1997). Beta-globin haplotypes from blood spots for follow-up of newborn hemoglobinopathy screening. American Journal of Hematology. 54(1). 76–78. 4 indexed citations
18.
Huether, Carl A., et al.. (1997). Epidemiologic Study of Down Syndrome in a Racially Diverse California Population, 1989-1991. American Journal of Epidemiology. 145(2). 134–147. 88 indexed citations
19.
Lorey, Fred, et al.. (1996). Distribution of hemoglobinopathy variants by ethnicity in a multiethnic state. Genetic Epidemiology. 13(5). 501–512. 95 indexed citations
20.
Lorey, Fred, et al.. (1994). Universal Screening forHemoglobinopathies UsingHigh-Performance LiquidChromatography: Clinical Resultsof 2.2 Million Screens. European Journal of Human Genetics. 2(4). 262–271. 50 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026