David Rodriguez‐Buritica

2.4k total citations
37 papers, 429 citations indexed

About

David Rodriguez‐Buritica is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David Rodriguez‐Buritica has authored 37 papers receiving a total of 429 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David Rodriguez‐Buritica's work include Connective tissue disorders research (8 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Metabolism and Genetic Disorders (4 papers). David Rodriguez‐Buritica is often cited by papers focused on Connective tissue disorders research (8 papers), Glycogen Storage Diseases and Myoclonus (5 papers) and Metabolism and Genetic Disorders (4 papers). David Rodriguez‐Buritica collaborates with scholars based in United States, Netherlands and France. David Rodriguez‐Buritica's co-authors include Anjali Aggarwal, S. Shahrukh Hashmi, Hope Northrup, Richard M. Pauli, Janet M. Legare, Peggy Modaff, Julie Hoover‐Fong, Michael B. Bober, Jacqueline T. Hecht and Terry G. J. Derks and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

David Rodriguez‐Buritica

30 papers receiving 424 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Rodriguez‐Buritica United States	12	227	161	76	74	54	37	429
Kei Takasawa Japan	13	187 0.8×	247 1.5×	53 0.7×	91 1.2×	43 0.8×	64	456
Sebastian Franik Netherlands	13	88 0.4×	98 0.6×	132 1.7×	93 1.3×	34 0.6×	19	819
Pao‐Chin Chiu Taiwan	12	53 0.2×	161 1.0×	108 1.4×	57 0.8×	54 1.0×	39	417
Manuel Anderegg Switzerland	13	78 0.3×	192 1.2×	145 1.9×	73 1.0×	91 1.7×	22	498
Amy Gaviglio United States	11	78 0.3×	167 1.0×	56 0.7×	38 0.5×	92 1.7×	30	417
Ahmed Khattab United States	11	106 0.5×	247 1.5×	138 1.8×	41 0.6×	21 0.4×	36	450
Prapai Dejkhamron Thailand	11	79 0.3×	93 0.6×	38 0.5×	37 0.5×	19 0.4×	36	314
Guanping Dong China	13	136 0.6×	150 0.9×	54 0.7×	93 1.3×	10 0.2×	51	471
Sechin Cho United States	11	64 0.3×	106 0.7×	81 1.1×	108 1.5×	21 0.4×	17	463
Young‐Lim Shin South Korea	11	121 0.5×	140 0.9×	10 0.1×	124 1.7×	61 1.1×	29	400

Countries citing papers authored by David Rodriguez‐Buritica

Since Specialization

Citations

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

Fields of papers citing papers by David Rodriguez‐Buritica

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Rodriguez‐Buritica. 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 David Rodriguez‐Buritica. The network helps show where David Rodriguez‐Buritica may publish in the future.

Co-authorship network of co-authors of David Rodriguez‐Buritica

This figure shows the co-authorship network connecting the top 25 collaborators of David Rodriguez‐Buritica. A scholar is included among the top collaborators of David Rodriguez‐Buritica 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 David Rodriguez‐Buritica. David Rodriguez‐Buritica 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

Weinstein, David A., Terry G. J. Derks, David Rodriguez‐Buritica, et al.. (2025). Safety and Efficacy of DTX401 , an AAV8 ‐Mediated Liver‐Directed Gene Therapy, in Adults With Glycogen Storage Disease Type I a ( GSDIa ). Journal of Inherited Metabolic Disease. 48(2). e70014–e70014. 7 indexed citations

Legare, Janet M., David G. Ingram, Richard M. Pauli, et al.. (2025). Evolution of sleep disordered breathing in infants with achondroplasia. Sleep And Breathing. 29(1). 88–88.

Hill, Jeremy P., Kathleen Shields, David Rodriguez‐Buritica, Laura S. Farach, & Paul Hillman. (2023). P192: Heterozygous ACTB pathogenic variant causing Baraitser-Winter syndrome presenting with tracheal ring, intestinal atresia, and neonatal diabetes. SHILAP Revista de lepidopterología. 1(1). 100221–100221.

Roberts, P. D., et al.. (2023). Arginase deficiency masked by cerebral palsy and coagulopathy—Three varied presentations of Latin American origin. JIMD Reports. 64(6). 434–439. 1 indexed citations

Rodriguez‐Buritica, David, et al.. (2023). Dermatological concerns for women and girls with turner syndrome. Frontiers in Medicine. 10. 1235187–1235187. 1 indexed citations

Nahm, Nickolas J., William G. Mackenzie, William G. Mackenzie, et al.. (2023). Achondroplasia natural history study (CLARITY): 60-year experience in orthopedic surgery from four skeletal dysplasia centers. Orphanet Journal of Rare Diseases. 18(1). 139–139. 10 indexed citations

Langley, Elizabeth, Laura S. Farach, Mary Kay Koenig, et al.. (2022). NEXMIF pathogenic variants in individuals of Korean, Vietnamese, and Mexican descent. American Journal of Medical Genetics Part A. 188(6). 1688–1692. 3 indexed citations

Rodriguez‐Buritica, David, Ayesha Ahmad, Terry G. J. Derks, et al.. (2022). COHORT 1-4 RESULTS FROM A PHASE 1/2 CLINICAL TRIAL OF AN AAV8-MEDIATED LIVER-DIRECTED GENE THERAPY IN ADULTS WITH GLYCOGEN STORAGE DISEASE TYPE IA (GSDIA). Molecular Genetics and Metabolism. 135(4). 296–296.

Rodriguez‐Buritica, David, et al.. (2022). Laparoscopic ovarian tissue harvesting for cryopreservation from a child with galactosemia. Fertility and Sterility. 118(5). 982–984. 3 indexed citations

10.

Mowrey, Kate, Hope Northrup, S. Shahrukh Hashmi, & David Rodriguez‐Buritica. (2022). Expanding Our Knowledge of Menstrual Irregularities Reported by Females With Tuberous Sclerosis Complex. SHILAP Revista de lepidopterología. 4. 798983–798983.

11.

Derks, Terry G. J., David Rodriguez‐Buritica, Ayesha Ahmad, et al.. (2021). Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs. Nutrients. 13(11). 3828–3828. 35 indexed citations

12.

Hoover‐Fong, Julie, S. Shahrukh Hashmi, Jacqueline T. Hecht, et al.. (2021). Achondroplasia Natural History Study (CLARITY): a multicenter retrospective cohort study of achondroplasia in the United States. Genetics in Medicine. 23(8). 1498–1505. 36 indexed citations

13.

Hoover‐Fong, Julie, Kerry Schulze, Michael B. Bober, et al.. (2021). Growth in achondroplasia including stature, weight, weight-for-height and head circumference from CLARITY: achondroplasia natural history study—a multi-center retrospective cohort study of achondroplasia in the US. Orphanet Journal of Rare Diseases. 16(1). 522–522. 33 indexed citations

14.

Bashamboo, Anu, Caroline Eozénou, Anne Jørgensen, et al.. (2018). Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. The American Journal of Human Genetics. 102(3). 487–493. 65 indexed citations

15.

Bashamboo, Anu, Caroline Eozénou, Annemette Jørgensen, et al.. (2018). Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. Yearbook of pediatric endocrinology. 2 indexed citations

16.

Aggarwal, Anjali, et al.. (2017). Marshall-Smith syndrome: Novel pathogenic variant and previously unreported associations with precocious puberty and aortic root dilatation. European Journal of Medical Genetics. 60(7). 391–394. 6 indexed citations

17.

Aggarwal, Anjali & David Rodriguez‐Buritica. (2017). Monogenic Hypertension in Children: A Review With Emphasis on Genetics. Advances in Chronic Kidney Disease. 24(6). 372–379. 8 indexed citations

18.

Aggarwal, Anjali, David Rodriguez‐Buritica, & Hope Northrup. (2017). Wiedemann-Steiner syndrome: Novel pathogenic variant and review of literature. European Journal of Medical Genetics. 60(6). 285–288. 23 indexed citations

19.

Rodriguez‐Buritica, David. (2015). Overview of genetics of disorders of sexual development. Current Opinion in Pediatrics. 27(6). 675–684. 13 indexed citations

20.

Nicola, Juan P., Andrea Reyna‐Neyra, Paul Saenger, et al.. (2015). Sodium/Iodide Symporter Mutant V270E Causes Stunted Growth but No Cognitive Deficiency. The Journal of Clinical Endocrinology & Metabolism. 100(10). E1353–E1361. 26 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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