Robert L. Conway

2.1k total citations
23 papers, 723 citations indexed

About

Robert L. Conway is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Robert L. Conway has authored 23 papers receiving a total of 723 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Pediatrics, Perinatology and Child Health and 8 papers in Clinical Biochemistry. Recurrent topics in Robert L. Conway's work include Metabolism and Genetic Disorders (8 papers), Neonatal Health and Biochemistry (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Robert L. Conway is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Neonatal Health and Biochemistry (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Robert L. Conway collaborates with scholars based in United States, Canada and United Kingdom. Robert L. Conway's co-authors include John M. Graham, William B. Dobyns, Ghayda Mirzaa, Dawn H. Siegel, Elizabeth Hopkins, Dorit Lev, Nancy Kramer, Tally Lerman‐Sagie, Elaine H. Zackai and Karen W. Gripp and has published in prestigious journals such as Nature Genetics, Clinica Chimica Acta and Human Mutation.

In The Last Decade

Robert L. Conway

22 papers receiving 705 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert L. Conway United States 13 338 298 147 119 115 23 723
Aleksandra Jezela‐Stanek Poland 14 367 1.1× 212 0.7× 116 0.8× 43 0.4× 84 0.7× 79 653
Elly Verbeek Netherlands 12 372 1.1× 120 0.4× 180 1.2× 89 0.7× 50 0.4× 15 901
Pilar Magoulas United States 15 383 1.1× 290 1.0× 57 0.4× 132 1.1× 73 0.6× 24 727
Yasutsugu Chinen Japan 15 269 0.8× 209 0.7× 371 2.5× 81 0.7× 18 0.2× 38 736
Hamad Alzaidan Saudi Arabia 14 283 0.8× 173 0.6× 55 0.4× 66 0.6× 67 0.6× 39 578
Hyon J. Kim South Korea 14 191 0.6× 292 1.0× 60 0.4× 112 0.9× 29 0.3× 28 532
Adi Mory Israel 15 245 0.7× 147 0.5× 76 0.5× 61 0.5× 38 0.3× 40 592
Reeval Segel Israel 18 649 1.9× 249 0.8× 39 0.3× 211 1.8× 87 0.8× 40 1.1k
Alina Kurolap Israel 12 150 0.4× 118 0.4× 89 0.6× 61 0.5× 36 0.3× 42 399
Nina Aula Finland 8 258 0.8× 72 0.2× 353 2.4× 74 0.6× 22 0.2× 10 616

Countries citing papers authored by Robert L. Conway

Since Specialization
Citations

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

Fields of papers citing papers by Robert L. Conway

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert L. Conway. 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 Robert L. Conway. The network helps show where Robert L. Conway may publish in the future.

Co-authorship network of co-authors of Robert L. Conway

This figure shows the co-authorship network connecting the top 25 collaborators of Robert L. Conway. A scholar is included among the top collaborators of Robert L. Conway 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 Robert L. Conway. Robert L. Conway 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.
Conway, Robert L., et al.. (2022). Transcobalamin receptor deficiency in seven asymptomatic patients ascertained through newborn screening. American Journal of Medical Genetics Part A. 188(4). 1102–1108. 3 indexed citations
2.
Sanchez‐Lara, Pedro A., Katheryn Grand, Maria K. Haanpää, et al.. (2021). Thinking outside “The Box”: Case‐based didactics for medical education and the instructional legacy of Dr John M. Graham, Jr. American Journal of Medical Genetics Part A. 185(9). 2636–2645. 2 indexed citations
3.
Longo, Nicola, George A. Díaz, Uta Lichter‐Konecki, et al.. (2020). Glycerol phenylbutyrate efficacy and safety from an open label study in pediatric patients under 2 months of age with urea cycle disorders. Molecular Genetics and Metabolism. 132(1). 19–26. 10 indexed citations
4.
Ames, Elizabeth G., et al.. (2020). A cautionary tale of pyridoxine toxicity in cystathionine beta‐synthase deficiency detected by two‐tier newborn screening highlights the need for clear pyridoxine dosing guidelines. American Journal of Medical Genetics Part A. 182(11). 2704–2708. 2 indexed citations
5.
Lawless, Michael, et al.. (2018). Risk Factors for Dysphagia Following a Cervical Fusion in a Trauma Population. Cureus. 10(10). e3489–e3489. 4 indexed citations
6.
Conway, Robert L., Isabelle Thiffault, Carol Saunders, et al.. (2016). Neonatal progeriod syndrome associated with biallelic truncating variants in POLR3A. American Journal of Medical Genetics Part A. 170(12). 3343–3346. 27 indexed citations
7.
Vockley, Jerry, Joel Charrow, George A. Díaz, et al.. (2016). Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disorders. Molecular Genetics and Metabolism. 119(3). 223–231. 67 indexed citations
8.
9.
Merideth, Melissa A., Jennifer L. Sloan, Nancy Braverman, et al.. (2015). Methylmalonic acidemia (MMA) in pregnancy: a case series and literature review. Journal of Inherited Metabolic Disease. 38(5). 839–846. 18 indexed citations
10.
Spencer, Linda, Adil Al‐Nahhas, Justin Miller, et al.. (2014). Novel mutations causing biotinidase deficiency in individuals identified by newborn screening in Michigan including an unique intronic mutation that alters mRNA expression of the biotinidase gene. Molecular Genetics and Metabolism. 112(3). 242–246. 21 indexed citations
11.
Conway, Robert L., et al.. (2014). Outcomes of individuals with profound and partial biotinidase deficiency ascertained by newborn screening in Michigan over 25 years. Genetics in Medicine. 17(3). 205–209. 33 indexed citations
12.
Mirzaa, Ghayda, Robert L. Conway, John M. Graham, & William B. Dobyns. (2013). PIK3CA-Related Segmental Overgrowth. Europe PMC (PubMed Central). 37 indexed citations
13.
Banugaria, Suhrad G., Sean N. Prater, Judeth K. McGann, et al.. (2012). Bortezomib in the rapid reduction of high sustained antibody titers in disorders treated with therapeutic protein: lessons learned from Pompe disease. Genetics in Medicine. 15(2). 123–131. 70 indexed citations
14.
Mirzaa, Ghayda, Robert L. Conway, Karen W. Gripp, et al.. (2012). Megalencephaly‐capillary malformation (MCAP) and megalencephaly‐polydactyly‐polymicrogyria‐hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis. American Journal of Medical Genetics Part A. 158A(2). 269–291. 121 indexed citations
15.
Thiel, Christian, Georg F. Hoffmann, Kristen Hanson, et al.. (2011). Improved diagnostics lead to identification of three new patients with congenital disorder of glycosylation-Ip. Human Mutation. 33(3). 485–487. 29 indexed citations
16.
El‐Gharbawy, Areeg, et al.. (2011). An individually, modified approach to desensitize infants and young children with Pompe disease, and significant reactions to alglucosidase alfa infusions. Molecular Genetics and Metabolism. 104(1-2). 118–122. 26 indexed citations
17.
Conway, Robert L., Moise Danielpour, & John M. Graham. (2007). Surgical management of cerebellar tonsillar herniation in three patients with macrocephaly–cutis marmorata telangiectatica congenita. Journal of Neurosurgery Pediatrics. 106(4). 296–301. 14 indexed citations
18.
Conway, Robert L., Barry D. Pressman, William B. Dobyns, et al.. (2007). Neuroimaging findings in macrocephaly–capillary malformation: A longitudinal study of 17 patients. American Journal of Medical Genetics Part A. 143A(24). 2981–3008. 78 indexed citations
19.
Ballif, Blake C., Elizabeth S. Jenkins, Suneeta Madan‐Khetarpal, et al.. (2007). Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2. Nature Genetics. 39(9). 1071–1073. 140 indexed citations
20.
Farrugia, Maria Elena, Robert L. Conway, Duncan Simpson, & Kathreena M. Kurian. (2004). Paraneoplastic limbic encephalitis. Clinical Neurology and Neurosurgery. 107(2). 128–131. 12 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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