Lisa E. Kratz

3.2k total citations
63 papers, 2.0k citations indexed

About

Lisa E. Kratz is a scholar working on Molecular Biology, Surgery and Immunology. According to data from OpenAlex, Lisa E. Kratz has authored 63 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 21 papers in Surgery and 12 papers in Immunology. Recurrent topics in Lisa E. Kratz's work include Cholesterol and Lipid Metabolism (20 papers), Peroxisome Proliferator-Activated Receptors (14 papers) and Metabolism and Genetic Disorders (10 papers). Lisa E. Kratz is often cited by papers focused on Cholesterol and Lipid Metabolism (20 papers), Peroxisome Proliferator-Activated Receptors (14 papers) and Metabolism and Genetic Disorders (10 papers). Lisa E. Kratz collaborates with scholars based in United States, Canada and India. Lisa E. Kratz's co-authors include Richard I. Kelley, Ann B. Moser, Christopher Cunniff, Marvin R. Natowicz, Moyra Smith, Hans C. Andersson, Elaine Tierney, Cedric Shackleton, Gail E. Herman and Nancy Braverman and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and PLoS ONE.

In The Last Decade

Lisa E. Kratz

61 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lisa E. Kratz United States	28	1.3k	784	415	205	199	63	2.0k
Helge Boman Norway	26	1.1k 0.8×	212 0.3×	488 1.2×	129 0.6×	173 0.9×	73	2.1k
Ben J. H. M. Poorthuis Netherlands	36	1.5k 1.2×	298 0.4×	212 0.5×	55 0.3×	105 0.5×	61	4.8k
Takamitsu Hori Japan	17	1.1k 0.8×	189 0.2×	266 0.6×	185 0.9×	229 1.2×	59	1.9k
Stephan Rust Germany	30	2.0k 1.6×	1.9k 2.4×	418 1.0×	558 2.7×	397 2.0×	63	3.9k
Kees Fluiter Netherlands	30	1.6k 1.3×	339 0.4×	214 0.5×	747 3.6×	334 1.7×	53	2.7k
Randall A. Heidenreich United States	25	722 0.6×	330 0.4×	194 0.5×	82 0.4×	75 0.4×	46	2.0k
Akira Ohtake Japan	27	1.9k 1.5×	218 0.3×	318 0.8×	122 0.6×	81 0.4×	138	2.7k
Saptarsi M. Haldar United States	30	2.3k 1.8×	334 0.4×	373 0.9×	344 1.7×	293 1.5×	54	3.6k
Xuefan Gu China	27	1.4k 1.1×	170 0.2×	540 1.3×	58 0.3×	84 0.4×	217	2.5k
Howard C. Haspel United States	20	1.3k 1.0×	397 0.5×	143 0.3×	246 1.2×	46 0.2×	33	1.8k

Countries citing papers authored by Lisa E. Kratz

Since Specialization

Citations

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

Fields of papers citing papers by Lisa E. Kratz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lisa E. Kratz. 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 Lisa E. Kratz. The network helps show where Lisa E. Kratz may publish in the future.

Co-authorship network of co-authors of Lisa E. Kratz

This figure shows the co-authorship network connecting the top 25 collaborators of Lisa E. Kratz. A scholar is included among the top collaborators of Lisa E. Kratz 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 Lisa E. Kratz. Lisa E. Kratz 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

Kratz, Lisa E., et al.. (2023). The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post‐mortem. JIMD Reports. 64(3). 233–237. 1 indexed citations

Martin, Renan Paulo, Elizabeth Wohler, Shaima Salman, et al.. (2022). Disruption of the HIF-1 pathway in individuals with Ollier disease and Maffucci syndrome. PLoS Genetics. 18(12). e1010504–e1010504. 9 indexed citations

Yoganathan, Sangeetha, et al.. (2021). Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1. Annals of Indian Academy of Neurology. 24(2). 259–261. 1 indexed citations

Arunachal, Gautham, Sangeetha Yoganathan, Lisa E. Kratz, et al.. (2020). Guanidinoacetate methyltransferase (GAMT) deficiency, a cerebral creatine deficiency syndrome: A rare treatable metabolic disorder. Annals of Indian Academy of Neurology. 23(3). 419–419. 5 indexed citations

Biase, Irene De, Silvia Tortorelli, Lisa E. Kratz, et al.. (2019). Laboratory diagnosis of disorders of peroxisomal biogenesis and function: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 22(4). 686–697. 14 indexed citations

Smith‐Hicks, Constance, Siddharth Gupta, Joshua B. Ewen, et al.. (2017). Randomized open-label trial of dextromethorphan in Rett syndrome. Neurology. 89(16). 1684–1690. 37 indexed citations

Chong, Karen, et al.. (2017). Severe phenotype of X‐linked dominant chondrodysplasia punctata. Clinical Case Reports. 5(9). 1435–1437.

Driver, Ashley M., Lisa E. Kratz, Richard I. Kelley, & Rolf W. Stottmann. (2016). Altered cholesterol biosynthesis causes precocious neurogenesis in the developing mouse forebrain. Neurobiology of Disease. 91. 69–82. 25 indexed citations

Gabitova, Linara, Diana Restifo, Andrey Gorin, et al.. (2015). Endogenous Sterol Metabolites Regulate Growth of EGFR/KRAS-Dependent Tumors via LXR. Cell Reports. 12(11). 1927–1938. 61 indexed citations

10.

He, Miao, Lisa E. Kratz, Joshua J. Michel, et al.. (2011). Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay. Journal of Clinical Investigation. 121(3). 976–984. 82 indexed citations

11.

Williams, Jason A., Christopher J. Barreiro, Lois U. Nwakanma, et al.. (2006). Valproic Acid Prevents Brain Injury in a Canine Model of Hypothermic Circulatory Arrest: A Promising New Approach to Neuroprotection During Cardiac Surgery. The Annals of Thoracic Surgery. 81(6). 2235–2242. 21 indexed citations

12.

Craig, Wendy Y., James E. Haddow, Glenn E. Palomaki, et al.. (2006). Identifying Smith–Lemli–Opitz syndrome in conjunction with prenatal screening for Down syndrome. Prenatal Diagnosis. 26(9). 842–849. 34 indexed citations

13.

Barreiro, Christopher J., Jason A. Williams, Torin P. Fitton, et al.. (2006). Noninvasive Assessment of Brain Injury in a Canine Model of Hypothermic Circulatory Arrest Using Magnetic Resonance Spectroscopy. The Annals of Thoracic Surgery. 81(5). 1593–1598. 18 indexed citations

14.

Shackleton, Cedric, Esther Roitman, Lisa E. Kratz, & Richard I. Kelley. (2001). Dehydro-oestriol and dehydropregnanetriol are candidate analytes for prenatal diagnosis of Smith-Lemli-Opitz syndrome. Prenatal Diagnosis. 21(3). 207–212. 32 indexed citations

15.

Shackleton, Cedric, Esther Roitman, Lisa E. Kratz, & Richard I. Kelley. (1999). Equine Type Estrogens Produced by a Pregnant Woman Carrying a Smith-Lemli-Opitz Syndrome Fetus. The Journal of Clinical Endocrinology & Metabolism. 84(3). 1157–1159. 28 indexed citations

16.

Kelley, Richard I., et al.. (1999). Abnormal sterol metabolism in patients with Conradi-H�nermann-Happle syndrome and sporadic lethal chondrodysplasia punctata. American Journal of Medical Genetics. 83(3). 213–219. 96 indexed citations

17.

Braverman, Nancy, Paul Lin, Fabian F. Moebius, et al.. (1999). Mutations in the gene encoding 3β- hydroxysteroid-Δ8,Δ7- isomerase cause X-linked dominant Conradi-Hünermann syndrome. Nature Genetics. 22(3). 291–294. 197 indexed citations

18.

Smith, Richard H., et al.. (1991). 1,3-Dialkyltriazenes: reactive intermediates and DNA alkylation. Chemical Research in Toxicology. 4(3). 334–340. 6 indexed citations

19.

Kratz, Lisa E., Joann A. Boughman, Theodore Pincus, David I. Cohen, & Barbara White Needleman. (1990). Association of scleroderma with a t cell antigen receptor γ gene restriction fragment length polymorphism. Arthritis & Rheumatism. 33(4). 569–573. 12 indexed citations

20.

Singer, Sanford S., et al.. (1987). A comparison ofin vivoandin vitrometabolites of the H1-antagonistN, N-dimethyl-N'-2-pyridyl-N'-(2-thienylmethyl)- 1,2-ethanediamine (methapyrilene) in the rat. Xenobiotica. 17(11). 1279–1291. 6 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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