Cindy Pham Lorentz

655 total citations
9 papers, 438 citations indexed

About

Cindy Pham Lorentz is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Cindy Pham Lorentz has authored 9 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in Cindy Pham Lorentz's work include Genomic variations and chromosomal abnormalities (4 papers), Metabolism and Genetic Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Cindy Pham Lorentz is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Metabolism and Genetic Disorders (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Cindy Pham Lorentz collaborates with scholars based in United States and Uganda. Cindy Pham Lorentz's co-authors include Syed M. Jalal, Rhett P. Ketterling, Regina Ensenauer, Virginia V. Michels, Heather C. Flynn, Anita S. Kulharya, D. Brian Dawson, Robin D. Clark, Adewale Adeyinka and Noralane M. Lindor and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Mayo Clinic Proceedings.

In The Last Decade

Cindy Pham Lorentz

9 papers receiving 426 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cindy Pham Lorentz United States 8 294 287 78 77 64 9 438
Marie McDonald United States 8 207 0.7× 308 1.1× 73 0.9× 48 0.6× 53 0.8× 13 505
Christian Wentzel Sweden 7 188 0.6× 196 0.7× 45 0.6× 23 0.3× 112 1.8× 8 373
Jostein Westvik Norway 9 172 0.6× 246 0.9× 37 0.5× 21 0.3× 35 0.5× 14 364
Winnie Courtens Belgium 16 431 1.5× 256 0.9× 23 0.3× 81 1.1× 158 2.5× 29 587
Sandesh C. Sreenath Nagamani United States 6 218 0.7× 194 0.7× 20 0.3× 18 0.2× 70 1.1× 8 349
Margaret N. Berry United States 9 109 0.4× 182 0.6× 61 0.8× 23 0.3× 37 0.6× 15 275
Rachel Slaugh United States 7 104 0.4× 227 0.8× 118 1.5× 9 0.1× 24 0.4× 11 307
Stephanie Demuth Germany 9 205 0.7× 270 0.9× 13 0.2× 14 0.2× 54 0.8× 11 407
Konstantina Kosma Greece 10 137 0.5× 130 0.5× 44 0.6× 17 0.2× 37 0.6× 30 288
Altuğ Koç Türkiye 11 157 0.5× 107 0.4× 16 0.2× 33 0.4× 80 1.3× 53 356

Countries citing papers authored by Cindy Pham Lorentz

Since Specialization
Citations

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

Fields of papers citing papers by Cindy Pham Lorentz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cindy Pham Lorentz. 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 Cindy Pham Lorentz. The network helps show where Cindy Pham Lorentz may publish in the future.

Co-authorship network of co-authors of Cindy Pham Lorentz

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

All Works

9 of 9 papers shown
1.
Sarafoglou, Kyriakie, Amy Gaviglio, Cindy Pham Lorentz, et al.. (2024). Can Incorporating Molecular Testing Improve the Accuracy of Newborn Screening for Congenital Adrenal Hyperplasia?. The Journal of Clinical Endocrinology & Metabolism. 110(4). e1194–e1203. 1 indexed citations
2.
Sarafoglou, Kyriakie, et al.. (2011). Molecular testing in congenital adrenal hyperplasia due to 21α‐hydroxylase deficiency in the era of newborn screening. Clinical Genetics. 82(1). 64–70. 13 indexed citations
3.
Utz, Jeanine, et al.. (2011). START, a double blind, placebo-controlled pharmacogenetic test of responsiveness to sapropterin dihydrochloride in phenylketonuria patients. Molecular Genetics and Metabolism. 105(2). 193–197. 38 indexed citations
4.
Lorentz, Cindy Pham, et al.. (2005). Subtelomere deletions and translocations are frequently familial. American Journal of Medical Genetics Part A. 135A(1). 28–35. 32 indexed citations
5.
Stockero, Kimberly J., et al.. (2004). Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb. Genetics in Medicine. 6(6). 517–520. 21 indexed citations
6.
Jalal, Syed M., Gurbax S. Sekhon, Cindy Pham Lorentz, et al.. (2003). Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients. Genetics in Medicine. 5(1). 28–34. 42 indexed citations
7.
Ensenauer, Regina, Adewale Adeyinka, Heather C. Flynn, et al.. (2003). Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients. The American Journal of Human Genetics. 73(5). 1027–1040. 265 indexed citations
8.
Lorentz, Cindy Pham, Syed M. Jalal, Dana M. Thompson, & Dusica Babovic‐Vuksanovic. (2002). Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies. American Journal of Medical Genetics. 111(1). 61–67. 11 indexed citations
9.
Lorentz, Cindy Pham, Eric D. Wieben, Ayalew Tefferi, David Whiteman, & Gordon W. Dewald. (2002). Primer on Medical Genomics Part I: History of Genetics and Sequencing of the Human Genome. Mayo Clinic Proceedings. 77(8). 773–782. 15 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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