Madeleine D. Harbison

2.7k total citations
34 papers, 1.5k citations indexed

About

Madeleine D. Harbison is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Madeleine D. Harbison has authored 34 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 21 papers in Genetics and 11 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Madeleine D. Harbison's work include Genetic Syndromes and Imprinting (14 papers), Sexual Differentiation and Disorders (9 papers) and Epigenetics and DNA Methylation (7 papers). Madeleine D. Harbison is often cited by papers focused on Genetic Syndromes and Imprinting (14 papers), Sexual Differentiation and Disorders (9 papers) and Epigenetics and DNA Methylation (7 papers). Madeleine D. Harbison collaborates with scholars based in United States, France and United Kingdom. Madeleine D. Harbison's co-authors include Joseph M. Gertner, Michael P. Wajnrajch, Rudolph L. Leibel, Streamson C. Chua, Irène Netchine, Salah Azzi, Maria I. New, John W. Funder, Maria G. Vogiatzi and Ji‐Qing Wei and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Journal of the American College of Cardiology.

In The Last Decade

Madeleine D. Harbison

34 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Madeleine D. Harbison United States 19 876 798 708 334 190 34 1.5k
Ayako Tanae Japan 14 789 0.9× 624 0.8× 345 0.5× 121 0.4× 100 0.5× 67 1.1k
Joyce F. Haskell United States 18 626 0.7× 651 0.8× 263 0.4× 101 0.3× 210 1.1× 26 1.3k
Blair E. Cox United States 18 366 0.4× 451 0.6× 182 0.3× 194 0.6× 361 1.9× 22 1.5k
Katherine L. Pratt United States 15 454 0.5× 666 0.8× 592 0.8× 94 0.3× 175 0.9× 22 1.6k
Yardena Tenenbaum‐Rakover Israel 20 609 0.7× 537 0.7× 395 0.6× 119 0.4× 135 0.7× 52 1.3k
E. Fernqvist‐Forbes Sweden 14 384 0.4× 689 0.9× 390 0.6× 61 0.2× 453 2.4× 18 1.2k
Craig C. Orlowski United States 14 497 0.6× 885 1.1× 245 0.3× 188 0.6× 182 1.0× 19 1.1k
Toru Momoi Japan 17 334 0.4× 310 0.4× 218 0.3× 159 0.5× 107 0.6× 40 921
J. Silver Israel 19 447 0.5× 225 0.3× 541 0.8× 263 0.8× 119 0.6× 39 1.9k
Caterina Di Cosmo Italy 20 328 0.4× 934 1.2× 230 0.3× 141 0.4× 76 0.4× 38 1.2k

Countries citing papers authored by Madeleine D. Harbison

Since Specialization
Citations

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

Fields of papers citing papers by Madeleine D. Harbison

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Madeleine D. Harbison. 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 Madeleine D. Harbison. The network helps show where Madeleine D. Harbison may publish in the future.

Co-authorship network of co-authors of Madeleine D. Harbison

This figure shows the co-authorship network connecting the top 25 collaborators of Madeleine D. Harbison. A scholar is included among the top collaborators of Madeleine D. Harbison 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 Madeleine D. Harbison. Madeleine D. Harbison 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.
Habib, Walid Abi, Frédéric Brioude, Salah Azzi, et al.. (2019). Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders. Science Advances. 5(2). eaau9425–eaau9425. 33 indexed citations
2.
Heide, Solveig, Sandra Chantot‐Bastaraud, Boris Keren, et al.. (2017). Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences. Journal of Medical Genetics. 55(3). 205–213. 34 indexed citations
3.
Habib, Walid Abi, Frédéric Brioude, Thomas Édouard, et al.. (2017). Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction. Genetics in Medicine. 20(2). 250–258. 98 indexed citations
4.
Chantot‐Bastaraud, Sandra, Frédéric Brioude, Matthias Begemann, et al.. (2017). Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction. Molecular Cytogenetics. 10(1). 28–28. 20 indexed citations
5.
Khattab, Ahmed, Tony Yuen, Mabel Yau, et al.. (2015). A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype–phenotype nonconcordance. Annals of the New York Academy of Sciences. 1364(1). 5–10. 12 indexed citations
6.
Harbison, Madeleine D., Karen Lin‐Su, & Maria I. New. (2011). Growth Hormone Treatment in Children with Congenital Adrenal Hyperplasia. Advances in experimental medicine and biology. 707. 107–107. 3 indexed citations
7.
Lin‐Su, Karen, Madeleine D. Harbison, Oksana Lekarev, Maria G. Vogiatzi, & Maria I. New. (2011). Final Adult Height in Children with Congenital Adrenal Hyperplasia Treated with Growth Hormone. The Journal of Clinical Endocrinology & Metabolism. 96(6). 1710–1717. 39 indexed citations
8.
Sharma, Jayendra, et al.. (2009). Aortic distensibility and dilation in Turner’s syndrome. Cardiology in the Young. 19(6). 568–572. 27 indexed citations
9.
Lin‐Su, Karen, Maria G. Vogiatzi, I. Howard Marshall, et al.. (2005). Treatment with Growth Hormone and Luteinizing Hormone Releasing Hormone Analog Improves Final Adult Height in Children with Congenital Adrenal Hyperplasia. The Journal of Clinical Endocrinology & Metabolism. 90(6). 3318–3325. 73 indexed citations
10.
Ostad, Mir Abolfazl, David T. Mininberg, Madeleine D. Harbison, & Margret S. Magid. (1999). Thoracolumbar accessory penis: etiology, diagnosis, and management. Urology. 53(2). 425–427. 2 indexed citations
11.
Wilson, Robert, Madeleine D. Harbison, Ron S. Newfield, et al.. (1998). Examination of Genotype and Phenotype Relationships in 14 Patients with Apparent Mineralocorticoid Excess1. The Journal of Clinical Endocrinology & Metabolism. 83(7). 2244–2254. 138 indexed citations
12.
Friedman, Deborah, et al.. (1998). Aortic dilation in turner syndrome. Journal of the American College of Cardiology. 31. 29–29. 1 indexed citations
13.
Wajnrajch, Michael P., Joseph M. Gertner, Madeleine D. Harbison, Streamson C. Chua, & Rudolph L. Leibel. (1996). Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mouse. Nature Genetics. 12(1). 88–90. 229 indexed citations
14.
Donovan, William D., Paula W. Brill, Patricia Winchester, et al.. (1996). Congenital fusion of the fourth and fifth metacarpals associated with primary gonadal failure. Skeletal Radiology. 25(3). 269–271. 3 indexed citations
15.
Zoppi, S., Carol M. Wilson, Madeleine D. Harbison, et al.. (1993). Complete testicular feminization caused by an amino-terminal truncation of the androgen receptor with downstream initiation.. Journal of Clinical Investigation. 91(3). 1105–1112. 65 indexed citations
16.
Imbeaud, Sandrine, et al.. (1992). Variants of the anti-M�llerian hormone gene in a compound heterozygote with the persistent M�llerian duct syndrome and his family. Human Genetics. 90(4). 389–94. 53 indexed citations
17.
Harbison, Madeleine D., et al.. (1991). Anti-Müllerian hormone in three intersex conditions.. PubMed. 34(3-4). 226–32. 4 indexed citations
18.
Harbison, Madeleine D. & Joseph M. Gertner. (1990). Permissive Action of Growth Hormone on the Renal Response to Dietary Phosphorus Deprivation*. The Journal of Clinical Endocrinology & Metabolism. 70(4). 1035–1040. 39 indexed citations
19.
Harbison, Madeleine D., et al.. (1988). Molecular studies of the parental origin and nature of human X isochromosomes. Cytogenetic and Genome Research. 47(4). 217–222. 18 indexed citations
20.
Saal, Howard M., Madeleine D. Harbison, & Irène Netchine. (1978). [Silver Russell's syndrome].. PubMed. 148(5). 527–30. 3 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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