Katheryn Grand

910 total citations
27 papers, 219 citations indexed

About

Katheryn Grand is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Katheryn Grand has authored 27 papers receiving a total of 219 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 16 papers in Genetics and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Katheryn Grand's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Syndromes and Imprinting (4 papers). Katheryn Grand is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genetic Syndromes and Imprinting (4 papers). Katheryn Grand collaborates with scholars based in United States, Canada and Australia. Katheryn Grand's co-authors include Matthew A. Deardorff, Jennifer M. Kalish, Kelly A. Duffy, John M. Graham, Pedro A. Sanchez‐Lara, Tyler Mark Pierson, Kristin Zelley, Elizabeth Bhoj, Amber Begtrup and Makoto Tominaga and has published in prestigious journals such as The American Journal of Human Genetics, Cellular and Molecular Life Sciences and Frontiers in Pharmacology.

In The Last Decade

Katheryn Grand

26 papers receiving 217 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Katheryn Grand United States 8 130 92 31 31 30 27 219
Thipwimol Tim‐Aroon Thailand 8 102 0.8× 68 0.7× 17 0.5× 9 0.3× 17 0.6× 49 228
Mariateresa Falco Italy 9 94 0.7× 175 1.9× 27 0.9× 5 0.2× 46 1.5× 22 334
Gilberto K. Furuzawa Brazil 9 116 0.9× 74 0.8× 8 0.3× 14 0.5× 68 2.3× 14 222
Paulina Halat Poland 6 173 1.3× 58 0.6× 12 0.4× 7 0.2× 11 0.4× 8 259
Silvio Ferraris Italy 12 262 2.0× 42 0.5× 45 1.5× 3 0.1× 25 0.8× 12 370
Tamehito Onoe Japan 7 168 1.3× 235 2.6× 26 0.8× 12 0.4× 24 0.8× 15 334
Nada Quercia Canada 8 148 1.1× 95 1.0× 28 0.9× 3 0.1× 14 0.5× 17 256
Jolien S. Klein Wassink‐Ruiter Netherlands 6 144 1.1× 71 0.8× 10 0.3× 15 0.5× 28 0.9× 7 216
Manish Pungliya United States 7 275 2.1× 131 1.4× 8 0.3× 6 0.2× 14 0.5× 11 472
Fabio Sirchia Italy 9 103 0.8× 108 1.2× 33 1.1× 18 0.6× 18 0.6× 35 208

Countries citing papers authored by Katheryn Grand

Since Specialization
Citations

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

Fields of papers citing papers by Katheryn Grand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katheryn Grand

This figure shows the co-authorship network connecting the top 25 collaborators of Katheryn Grand. A scholar is included among the top collaborators of Katheryn Grand 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 Katheryn Grand. Katheryn Grand 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.
Grand, Katheryn, Pedro A. Sanchez‐Lara, Thierry Levade, et al.. (2025). Acid Ceramidase Deficiency. Neurology Genetics. 11(2). e200243–e200243.
2.
3.
Xie, Lingling, Miranda J. McDaniel, Riley E. Perszyk, et al.. (2023). Functional effects of disease-associated variants reveal that the S1–M1 linker of the NMDA receptor critically controls channel opening. Cellular and Molecular Life Sciences. 80(4). 110–110. 6 indexed citations
4.
Lee, Michelle M., Darryl C. De Vivo, Daniel Friedman, et al.. (2022). The clinical spectrum of SMA‐PME and in vitro normalization of its cellular ceramide profile. Annals of Clinical and Translational Neurology. 9(12). 1941–1952. 5 indexed citations
5.
Veale, Emma L., et al.. (2022). A KCNB1 gain of function variant causes developmental delay and speech apraxia but not seizures. Frontiers in Pharmacology. 13. 1093313–1093313. 6 indexed citations
6.
Grand, Katheryn, et al.. (2021). Genetic skin disorders: The value of a multidisciplinary clinic. American Journal of Medical Genetics Part A. 185(4). 1159–1167. 6 indexed citations
7.
Patel, Nisha, John M. Graham, Michael J. Bamshad, et al.. (2021). Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. American Journal of Medical Genetics Part A. 185(7). 2136–2149. 3 indexed citations
8.
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
9.
Grand, Katheryn, et al.. (2021). Whole genome sequencing identifies a cryptic SOX9 regulatory element duplication underlying a case of 46,XX ovotesticular difference of sexual development. American Journal of Medical Genetics Part A. 185(9). 2782–2788. 8 indexed citations
10.
Grand, Katheryn, Virginia Kimonis, Merlin G. Butler, et al.. (2021). Mosaic de novo SNRPN gene variant associated with Prader-Willi syndrome. Journal of Medical Genetics. 59(7). 719–722. 4 indexed citations
11.
Sheppard, Sarah E., Anna Smith, Katheryn Grand, et al.. (2020). Further delineation of the phenotypic spectrum of nevus comedonicus syndrome to include congenital pulmonary airway malformation of the lung and aneurysm. American Journal of Medical Genetics Part A. 182(4). 746–754. 6 indexed citations
12.
Grand, Katheryn, et al.. (2020). Expanding the phenotypic spectrum ofRPL13‐relatedskeletal dysplasia. American Journal of Medical Genetics Part A. 185(9). 2776–2781. 6 indexed citations
13.
Morleo, Manuela, Vincenzo Nigro, Annalaura Torella, et al.. (2020). Identification of an Identical de Novo SCAMP5 Missense Variant in Four Unrelated Patients With Seizures and Severe Neurodevelopmental Delay. Frontiers in Pharmacology. 11. 599191–599191. 3 indexed citations
14.
Smith, Robert J., Denise W. Metry, Matthew A. Deardorff, et al.. (2020). Segmental congenital hemangiomas: Three cases of a rare entity. Pediatric Dermatology. 37(3). 548–553. 4 indexed citations
15.
Davis, Shanlee, Matthew A. Deardorff, Katheryn Grand, et al.. (2019). Growth hormone deficiency in megalencephaly‐capillary malformation syndrome: An association with activating mutations in PIK3CA. American Journal of Medical Genetics Part A. 182(1). 162–168. 13 indexed citations
16.
Murali, Chaya N., Dong Li, Katheryn Grand, Håkon Håkonarson, & Elizabeth Bhoj. (2019). Isolated vocal cord paralysis in two siblings with compound heterozygous variants in MUSK: Expanding the phenotypic spectrum. American Journal of Medical Genetics Part A. 179(4). 655–658. 7 indexed citations
17.
Duffy, Kelly A., et al.. (2019). Beckwith–Wiedemann syndrome in diverse populations. American Journal of Medical Genetics Part A. 179(4). 525–533. 14 indexed citations
18.
Suzuki, Yoshiro, David Chitayat, Hirotake Sawada, et al.. (2018). TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism. The American Journal of Human Genetics. 102(6). 1104–1114. 54 indexed citations
19.
Katz, Lorraine E. Levitt, T. Blaine Crowley, Katheryn Grand, et al.. (2018). Association of hypocalcemia with congenital heart disease in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 176(10). 2099–2103. 6 indexed citations
20.
Grand, Katheryn, Lorraine E. Levitt Katz, T. Blaine Crowley, et al.. (2018). The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 176(10). 2167–2171. 4 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Thipwimol Tim‐Aroon Breakdown of academic impact, for papers by Mariateresa Falco Breakdown of academic impact, for papers by Gilberto K. Furuzawa Breakdown of academic impact, for papers by Paulina Halat Breakdown of academic impact, for papers by Silvio Ferraris Breakdown of academic impact, for papers by Tamehito Onoe Breakdown of academic impact, for papers by Nada Quercia Breakdown of academic impact, for papers by Jolien S. Klein Wassink‐Ruiter Breakdown of academic impact, for papers by Manish Pungliya Breakdown of academic impact, for papers by Fabio Sirchia
Rankless by CCL
2026