Andrew Lane

766 total citations
22 papers, 428 citations indexed

About

Andrew Lane is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Andrew Lane has authored 22 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Endocrinology, Diabetes and Metabolism and 6 papers in Genetics. Recurrent topics in Andrew Lane's work include Neonatal Respiratory Health Research (3 papers), Sexual Differentiation and Disorders (3 papers) and Growth Hormone and Insulin-like Growth Factors (3 papers). Andrew Lane is often cited by papers focused on Neonatal Respiratory Health Research (3 papers), Sexual Differentiation and Disorders (3 papers) and Growth Hormone and Insulin-like Growth Factors (3 papers). Andrew Lane collaborates with scholars based in United States, United Kingdom and Netherlands. Andrew Lane's co-authors include Murat Bastepe, Harald Jüppner, Thomas A. Wilson, David Tegay, Thomas Preston, Stacey Storch Bracken, Patricia Galvin‐Parton, Eli Hatchwell, Jasmin Roohi and Nadia Sattar and has published in prestigious journals such as The American Journal of Human Genetics, American Journal of Obstetrics and Gynecology and The Journal of Pediatrics.

In The Last Decade

Andrew Lane

20 papers receiving 411 citations

Peers

Andrew Lane
Weilai Dong United States
Alice S. Brooks Netherlands
Sara Bertok Slovenia
Julia E. Ostberg United Kingdom
E Strengman Netherlands
Weilai Dong United States
Andrew Lane
Citations per year, relative to Andrew Lane Andrew Lane (= 1×) peers Weilai Dong

Countries citing papers authored by Andrew Lane

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Lane

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Lane

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Lane. A scholar is included among the top collaborators of Andrew Lane 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 Andrew Lane. Andrew Lane 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.
Goldberg, I., et al.. (2022). Juvenile Granulosa Cell Tumor Mimicking HAIR-AN in a 4-year-old: A Case Report. Journal of Clinical Research in Pediatric Endocrinology. 16(2). 200–204.
2.
Galvin‐Parton, Patricia, et al.. (2021). Continuous Glucose Monitoring in the Management of Hypoglycemia in TANGO2. Journal of the Endocrine Society. 5(Supplement_1). A699–A699. 1 indexed citations
4.
Lane, Andrew, et al.. (2017). Opioid-induced hyponatremia in a patient with central diabetes insipidus: independence from ADH. Journal of Pediatric Endocrinology and Metabolism. 30(6). 693–696. 5 indexed citations
5.
Lekarev, Oksana, Andrew Lane, Guangyu Zhu, et al.. (2012). Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene. Journal of Perinatology. 33(1). 76–78. 16 indexed citations
6.
Avila, Cecilia, John Chen, Andrew Lane, et al.. (2011). 246: Fasting plasma active glucagon-like peptide-1 (GLP-1) in pregnancies with and without gestational diabetes (GDM). American Journal of Obstetrics and Gynecology. 204(1). S106–S106. 4 indexed citations
7.
Sattar, Nadia, et al.. (2010). Celiac Disease in Children, Adolescents, and Young Adults with Autoimmune Thyroid Disease. The Journal of Pediatrics. 158(2). 272–275.e1. 41 indexed citations
8.
Mileva, Izolda, et al.. (2010). The Effect of Oral Leucine on Protein Metabolism in Adolescents with Type 1 Diabetes Mellitus. International Journal of Pediatric Endocrinology. 2010. 1–6. 9 indexed citations
9.
Ott, Claus‐Eric, Gundula Leschik, Louise Brueton, et al.. (2010). Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation. 31(8). E1587–E1593. 58 indexed citations
10.
Kacer, Martin, et al.. (2008). Effect of Inspiration/Expiration on Height Measurement. Journal of Pediatric Endocrinology and Metabolism. 21(8). 763–9. 2 indexed citations
11.
Tegay, David, Andrew Lane, Jasmin Roohi, & Eli Hatchwell. (2007). Contiguous gene deletion involving L1CAM and AVPR2 causes X‐linked hydrocephalus with nephrogenic diabetes insipidus. American Journal of Medical Genetics Part A. 143A(6). 594–598. 18 indexed citations
12.
Blanco, E, et al.. (2006). Use of Subcutaneous DDAVP in Infants with Central Diabetes Insipidus. Journal of Pediatric Endocrinology and Metabolism. 19(7). 919–25. 18 indexed citations
13.
Preston, Thomas, et al.. (2006). Neurocognitive function in children with compensated hypothyroidism: lack of short term effects on or off thyroxin. BMC Endocrine Disorders. 6(1). 2–2. 36 indexed citations
14.
Lane, Andrew, et al.. (2004). Thyrotoxic Periodic Paralysis Associated with a Mutation in the Sodium Channel Gene SCN4A. Journal of Pediatric Endocrinology and Metabolism. 17(12). 1679–82. 24 indexed citations
15.
Whyte, Gregory P., et al.. (2003). Electrocardiography and Echocardiography Findings in Contemporary Dancers. Journal of Dance Medicine & Science. 7(3). 91–95. 6 indexed citations
16.
Lane, Andrew, et al.. (2002). Mosaic variegated aneuploidy with growth hormone deficiency and congenital heart defects. American Journal of Medical Genetics. 110(3). 273–277. 17 indexed citations
17.
Bastepe, Murat, Andrew Lane, & Harald Jüppner. (2001). Paternal Uniparental Isodisomy of Chromosome 20q—and the Resulting Changes in GNAS1 Methylation—as a Plausible Cause of Pseudohypoparathyroidism. The American Journal of Human Genetics. 68(5). 1283–1289. 146 indexed citations
18.
Lane, Andrew & Mary Lee. (2001). Müllerian inhibiting substance: a nontraditional marker of gonadal function. Current Opinion in Endocrinology & Diabetes. 8(6). 296–300. 2 indexed citations
19.
Galvin‐Parton, Patricia, et al.. (2000). Congenital nasal pyriform aperture stenosis associated with central diabetes insipidus. The Journal of Pediatrics. 137(2). 260–262. 13 indexed citations
20.
Lane, Andrew & Mary Lee. (1999). Clinical Applications of Müllerian Inhibiting Substance in Patients with Gonadal Disorders. The Endocrinologist. 9(3). 208–215. 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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