Joy Bryant

1.5k total citations
21 papers, 682 citations indexed

About

Joy Bryant is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Joy Bryant has authored 21 papers receiving a total of 682 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Joy Bryant's work include Genetic and Kidney Cyst Diseases (17 papers), Genetic Syndromes and Imprinting (10 papers) and Renal and related cancers (9 papers). Joy Bryant is often cited by papers focused on Genetic and Kidney Cyst Diseases (17 papers), Genetic Syndromes and Imprinting (10 papers) and Renal and related cancers (9 papers). Joy Bryant collaborates with scholars based in United States and United Kingdom. Joy Bryant's co-authors include William A. Gahl, Meral Gunay‐Aygun, Isa Bernardini, Roxanne Fischer, Peter L. Choyke, Theo Heller, Barış Türkbey, James C. Reynolds, Katie Piwnica–Worms and Vandana Sachdev and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The Journal of Pediatrics and Clinical Journal of the American Society of Nephrology.

In The Last Decade

Joy Bryant

21 papers receiving 669 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joy Bryant United States 15 448 388 140 126 97 21 682
Inderneel Sahai United States 12 122 0.3× 187 0.5× 191 1.4× 134 1.1× 50 0.5× 34 530
Linda M. Randolph United States 13 162 0.4× 176 0.5× 156 1.1× 147 1.2× 63 0.6× 31 552
Jingsi Luo China 13 197 0.4× 290 0.7× 62 0.4× 156 1.2× 29 0.3× 65 556
Florindo Mollica Italy 10 126 0.3× 228 0.6× 141 1.0× 178 1.4× 42 0.4× 25 471
Ilham Ratbi Morocco 15 162 0.4× 332 0.9× 65 0.5× 29 0.2× 52 0.5× 45 617
Amarilis Sanchez‐Valle United States 12 165 0.4× 289 0.7× 378 2.7× 82 0.7× 96 1.0× 26 642
Jürgen Herwig Germany 9 379 0.8× 157 0.4× 102 0.7× 33 0.3× 100 1.0× 12 705
Silvia Einaudi Italy 16 274 0.6× 465 1.2× 16 0.1× 102 0.8× 148 1.5× 30 903
Sunita Arya United States 9 94 0.2× 185 0.5× 125 0.9× 36 0.3× 44 0.5× 18 431
Naoki Yamaguchi Japan 10 162 0.4× 346 0.9× 353 2.5× 169 1.3× 179 1.8× 16 652

Countries citing papers authored by Joy Bryant

Since Specialization
Citations

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

Fields of papers citing papers by Joy Bryant

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joy Bryant

This figure shows the co-authorship network connecting the top 25 collaborators of Joy Bryant. A scholar is included among the top collaborators of Joy Bryant 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 Joy Bryant. Joy Bryant 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.
Rossignol, Francis, Monique B. Perry, Pim Suwannarat, et al.. (2024). Patient-reported outcomes and functional assessments of patients with Alkaptonuria in a 3-year Nitisinone treatment trial. Molecular Genetics and Metabolism. 143(1-2). 108562–108562. 2 indexed citations
2.
Font–Montgomery, Esperanza, Joy Bryant, Peter L. Choyke, et al.. (2020). Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis. Molecular Genetics and Metabolism. 131(1-2). 267–276. 11 indexed citations
3.
Waldman, Meryl, Joan C. Han, Joy Bryant, et al.. (2018). Alström syndrome: Renal findings in correlation with obesity, insulin resistance, dyslipidemia and cardiomyopathy in 38 patients prospectively evaluated at the NIH clinical center. Molecular Genetics and Metabolism. 125(1-2). 181–191. 13 indexed citations
4.
Han, Joan C., Chia‐Ying Liu, James C. Reynolds, et al.. (2018). Comprehensive Endocrine-Metabolic Evaluation of Patients With Alström Syndrome Compared With BMI-Matched Controls. The Journal of Clinical Endocrinology & Metabolism. 103(7). 2707–2719. 47 indexed citations
5.
Brewer, Carmen C., Olga Stakhovskaya, Joy Bryant, et al.. (2017). Auditory and otologic profile of Alström syndrome: Comprehensive single center data on 38 patients. American Journal of Medical Genetics Part A. 173(8). 2210–2218. 14 indexed citations
6.
Stephen, Joshi, Thierry Vilboux, Dawn Maynard, et al.. (2017). Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency. Human Genetics. 136(4). 399–408. 26 indexed citations
7.
Brofferio, Alessandra, Vandana Sachdev, Hwaida Hannoush, et al.. (2017). Characteristics of cardiomyopathy in Alström syndrome: Prospective single-center data on 38 patients. Molecular Genetics and Metabolism. 121(4). 336–343. 30 indexed citations
8.
Leschek, Ellen, et al.. (2017). Effect of Antiandrogen, Aromatase Inhibitor, and Gonadotropin-releasing Hormone Analog on Adult Height in Familial Male Precocious Puberty. The Journal of Pediatrics. 190. 229–235. 18 indexed citations
9.
Fleming, Leah, Daniel Doherty, Melissa A. Parisi, et al.. (2017). Prospective Evaluation of Kidney Disease in Joubert Syndrome. Clinical Journal of the American Society of Nephrology. 12(12). 1962–1973. 49 indexed citations
10.
Vilboux, Thierry, May Christine V. Malicdan, Joseph C. Roney, et al.. (2017). CELSR2, encoding a planar cell polarity protein, is a putative gene in Joubert syndrome with cortical heterotopia, microophthalmia, and growth hormone deficiency. American Journal of Medical Genetics Part A. 173(3). 661–666. 24 indexed citations
11.
Strongin, Anna, Theo Heller, Dan Doherty, et al.. (2017). Characteristics of Liver Disease in 100 Individuals With Joubert Syndrome Prospectively Evaluated at a Single Center. Journal of Pediatric Gastroenterology and Nutrition. 66(3). 428–435. 17 indexed citations
12.
Marshall, Jan D., et al.. (2016). Respiratory manifestations in 38 patients with Alström syndrome. Pediatric Pulmonology. 52(4). 487–493. 16 indexed citations
13.
Malicdan, May Christine V., Thierry Vilboux, Joshi Stephen, et al.. (2015). Mutations in human homologue of chicken talpid3 gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes. Journal of Medical Genetics. 52(12). 830–839. 35 indexed citations
14.
Banks, Nicole, Joy Bryant, Roxanne Fischer, et al.. (2014). Pregnancy in autosomal recessive polycystic kidney disease. Archives of Gynecology and Obstetrics. 291(3). 705–708. 9 indexed citations
15.
Gunay‐Aygun, Meral, Baris I. Turkbey, Joy Bryant, et al.. (2011). Hepatorenal findings in obligate heterozygotes for autosomal recessive polycystic kidney disease. Molecular Genetics and Metabolism. 104(4). 677–681. 37 indexed citations
16.
Introne, Wendy J., Monique B. Perry, James Troendle, et al.. (2011). A 3-year randomized therapeutic trial of nitisinone in alkaptonuria. Molecular Genetics and Metabolism. 103(4). 307–314. 141 indexed citations
17.
O’Brien, Kevin, Esperanza Font–Montgomery, Joy Bryant, et al.. (2011). Congenital Hepatic Fibrosis and Portal Hypertension in Autosomal Dominant Polycystic Kidney Disease. Journal of Pediatric Gastroenterology and Nutrition. 54(1). 83–89. 19 indexed citations
18.
Piwnica–Worms, Katie, Joy Bryant, Isa Bernardini, et al.. (2010). Fibrocystic disease of liver and pancreas; under‐recognized features of the X‐linked ciliopathy oral‐facial‐digital syndrome type 1 (OFD I). American Journal of Medical Genetics Part A. 152A(10). 2640–2645. 31 indexed citations
19.
Gunay‐Aygun, Meral, M. Tuchman, Esperanza Font–Montgomery, et al.. (2009). PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis. Molecular Genetics and Metabolism. 99(2). 160–173. 66 indexed citations
20.
Türkbey, Barış, İclal Ocak, Kailash Daryanani, et al.. (2008). Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF). Pediatric Radiology. 39(2). 100–111. 69 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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