Karen Kowal

2.0k total citations
23 papers, 1.3k citations indexed

About

Karen Kowal is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Karen Kowal has authored 23 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 17 papers in Molecular Biology and 6 papers in Reproductive Medicine. Recurrent topics in Karen Kowal's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (20 papers), Sexual Differentiation and Disorders (15 papers) and Sperm and Testicular Function (5 papers). Karen Kowal is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (20 papers), Sexual Differentiation and Disorders (15 papers) and Sperm and Testicular Function (5 papers). Karen Kowal collaborates with scholars based in United States, France and Netherlands. Karen Kowal's co-authors include Judith L. Ross, Andrew R. Zinn, F.F.B. Elder, Carole Samango‐Sprouse, Harvey Kushner, Najiba Lahlou, Martha Bardsley, Gordon B. Cutler, Penelope Feuillan and Charmian A. Quigley and has published in prestigious journals such as New England Journal of Medicine, The Journal of Clinical Endocrinology & Metabolism and European Heart Journal.

In The Last Decade

Karen Kowal

23 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karen Kowal United States 18 984 806 263 251 112 23 1.3k
Anne Skakkebæk Denmark 21 1.2k 1.2× 915 1.1× 345 1.3× 448 1.8× 65 0.6× 59 1.6k
B.J. Otten Netherlands 26 594 0.6× 987 1.2× 713 2.7× 244 1.0× 36 0.3× 55 1.7k
Andréa Trevas Maciel‐Guerra Brazil 20 1.1k 1.1× 1.2k 1.5× 220 0.8× 379 1.5× 59 0.5× 146 1.7k
Hassan Rouba Morocco 22 739 0.8× 762 0.9× 103 0.4× 419 1.7× 10 0.1× 83 1.4k
B. P. Hauffa Germany 16 635 0.6× 599 0.7× 297 1.1× 127 0.5× 19 0.2× 43 1.2k
J L Chaussain France 21 496 0.5× 681 0.8× 563 2.1× 517 2.1× 21 0.2× 62 1.4k
Miroslav Dumić Croatia 18 373 0.4× 599 0.7× 383 1.5× 50 0.2× 17 0.2× 54 1.0k
Sheila Youings United Kingdom 15 831 0.8× 428 0.5× 24 0.1× 51 0.2× 25 0.2× 18 978
Helena Sim Australia 13 554 0.6× 635 0.8× 33 0.1× 207 0.8× 12 0.1× 15 1.0k
P. Borrelli Italy 17 310 0.3× 330 0.4× 498 1.9× 266 1.1× 4 0.0× 40 1.0k

Countries citing papers authored by Karen Kowal

Since Specialization
Citations

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

Fields of papers citing papers by Karen Kowal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Kowal

This figure shows the co-authorship network connecting the top 25 collaborators of Karen Kowal. A scholar is included among the top collaborators of Karen Kowal 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 Karen Kowal. Karen Kowal 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.
Foland‐Ross, Lara C., et al.. (2023). Executive Dysfunction in Klinefelter Syndrome: Associations With Brain Activation and Testicular Failure. The Journal of Clinical Endocrinology & Metabolism. 109(1). e88–e95. 5 indexed citations
2.
Howell, Susan, Shanlee Davis, Mariah Brown, et al.. (2022). Noninvasive prenatal screening ( NIPS ) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance. Journal of Genetic Counseling. 32(1). 250–259. 1 indexed citations
3.
Davis, Shanlee, et al.. (2020). Testicular function in boys with 47,XYY and relationship to phenotype. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(2). 371–385. 14 indexed citations
4.
Tartaglia, Nicole, Susan Howell, Shanlee Davis, et al.. (2020). Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospectiveeXtraordinarYbabies study to identify early risk factors and targets for intervention. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(2). 428–443. 31 indexed citations
5.
Ross, Judith L., Harvey Kushner, Karen Kowal, et al.. (2017). Androgen Treatment Effects on Motor Function, Cognition, and Behavior in Boys with Klinefelter Syndrome. The Journal of Pediatrics. 185. 193–199.e4. 53 indexed citations
6.
Davis, Shanlee, et al.. (2016). Effects of Oxandrolone on Cardiometabolic Health in Boys with Klinefelter syndrome: A Randomized Controlled Trial. The Journal of Clinical Endocrinology & Metabolism. 102(1). jc.2016–2904. 36 indexed citations
7.
Bardsley, Martha, Karen Kowal, Nicole Tartaglia, et al.. (2013). 47,XYY Syndrome: Clinical Phenotype and Timing of Ascertainment. The Journal of Pediatrics. 163(4). 1085–1094. 110 indexed citations
8.
Ross, Judith L., Charmian A. Quigley, Dachuang Cao, et al.. (2011). Growth Hormone Plus Childhood Low-Dose Estrogen in Turner Syndrome. Obstetrical & Gynecological Survey. 66(8). 486–487. 3 indexed citations
9.
Ross, Judith L., Charmian A. Quigley, Dachuang Cao, et al.. (2011). Growth Hormone plus Childhood Low-Dose Estrogen in Turner's Syndrome. New England Journal of Medicine. 364(13). 1230–1242. 142 indexed citations
10.
Bardsley, Martha, Bonita Falkner, Karen Kowal, & Judith L. Ross. (2011). Insulin resistance and metabolic syndrome in prepubertal boys with Klinefelter syndrome. Acta Paediatrica. 100(6). 866–870. 60 indexed citations
11.
Shah, Kavita, et al.. (2010). Prospective Study Confirms Oxandrolone-Associated Improvement in Height in Growth Hormone-Treated Adolescent Girls with Turner Syndrome. Hormone Research in Paediatrics. 75(1). 38–46. 36 indexed citations
12.
Ross, Judith L., Michèle M. M. Mazzocco, Harvey Kushner, et al.. (2009). Effects of Treatment with Oxandrolone for 4 Years on the Frequency of Severe Arithmetic Learning Disability in Girls with Turner Syndrome. The Journal of Pediatrics. 155(5). 714–720. 21 indexed citations
13.
Zinn, Andrew R., Najiba Lahlou, Purita Ramos, et al.. (2007). Effect of Ascertainment and Genetic Features on the Phenotype of Klinefelter Syndrome. The Journal of Pediatrics. 152(5). 716–722. 71 indexed citations
14.
Zinn, Andrew R., David P. Roeltgen, Gerry A. Stefanatos, et al.. (2007). A Turner syndrome neurocognitive phenotype maps to Xp22.3. Behavioral and Brain Functions. 3(1). 24–24. 52 indexed citations
15.
Zinn, Andrew R., Purita Ramos, F.F.B. Elder, et al.. (2005). Androgen Receptor CAGnRepeat Length Influences Phenotype of 47,XXY (Klinefelter) Syndrome. The Journal of Clinical Endocrinology & Metabolism. 90(9). 5041–5046. 91 indexed citations
16.
Ross, Judith L., Carole Samango‐Sprouse, Najiba Lahlou, et al.. (2005). Early Androgen Deficiency in Infants and Young Boys with 47,XXY Klinefelter Syndrome. Hormone Research in Paediatrics. 64(1). 39–45. 117 indexed citations
17.
Ross, Judith L., Karen Kowal, Charmian A. Quigley, et al.. (2005). The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children with Leri-Weill Dyschondrosteosis and Turner Syndrome. The Journal of Pediatrics. 147(4). 499–507. 41 indexed citations
18.
Ross, Judith L., Charles I. Scott, Karen Kowal, et al.. (2001). Phenotypes Associated with SHOX Deficiency. The Journal of Clinical Endocrinology & Metabolism. 86(12). 5674–5680. 136 indexed citations
19.
Ross, Judith L., et al.. (1995). Lipid abnormalities in Turner syndrome. The Journal of Pediatrics. 126(2). 242–245. 78 indexed citations
20.
Wallukat, Gerd, et al.. (1991). Autoantibodies against the  -adrenergic receptor in human myocarditis and dilated cardiomyopathy:  -adrenergic agonism without desensitization. European Heart Journal. 12(suppl D). 178–181. 94 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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