Ian A. Glass

22.0k total citations · 1 hit paper
122 papers, 4.4k citations indexed

About

Ian A. Glass is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ian A. Glass has authored 122 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 65 papers in Genetics and 41 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ian A. Glass's work include Genetic and Kidney Cyst Diseases (23 papers), Fetal and Pediatric Neurological Disorders (22 papers) and Prenatal Screening and Diagnostics (16 papers). Ian A. Glass is often cited by papers focused on Genetic and Kidney Cyst Diseases (23 papers), Fetal and Pediatric Neurological Disorders (22 papers) and Prenatal Screening and Diagnostics (16 papers). Ian A. Glass collaborates with scholars based in United States, Australia and United Kingdom. Ian A. Glass's co-authors include Melissa A. Parisi, Dan Doherty, Phillip F. Chance, Craig L. Bennett, Cole Trapnell, William B. Dobyns, Diana R. O’Day, Kimberly A. Aldinger, Fan Zhang and Michael Zager and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Ian A. Glass

116 papers receiving 4.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A human cell atlas of fetal gene expression

2020 383 citations Junyue Cao, Diana R. O’Day et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ian A. Glass United States	36	2.9k	2.1k	1.1k	376	323	122	4.4k
Gabriele Gillessen‐Kaesbach Germany	38	2.8k 1.0×	2.8k 1.4×	949 0.8×	232 0.6×	468 1.4×	133	4.7k
Hilde Van Esch Belgium	40	3.5k 1.2×	3.5k 1.7×	629 0.6×	338 0.9×	259 0.8×	148	5.6k
Ankita Patel United States	42	2.8k 1.0×	4.1k 2.0×	1.7k 1.5×	219 0.6×	522 1.6×	143	6.5k
Hülya Kayserili Türkiye	35	2.8k 1.0×	1.7k 0.8×	473 0.4×	213 0.6×	331 1.0×	152	4.4k
Samantha J.L. Knight United Kingdom	38	3.0k 1.0×	4.0k 1.9×	657 0.6×	285 0.8×	210 0.7×	89	5.8k
Peter Wieacker Germany	35	2.4k 0.9×	1.6k 0.8×	397 0.4×	369 1.0×	191 0.6×	141	3.8k
Lina Basel‐Vanagaite Israel	32	1.9k 0.7×	1.4k 0.7×	497 0.4×	468 1.2×	233 0.7×	111	3.6k
Marc Jeanpierre France	37	3.8k 1.3×	1.3k 0.6×	515 0.5×	533 1.4×	309 1.0×	120	4.7k
Sylvie Odent France	36	2.7k 0.9×	1.5k 0.7×	562 0.5×	230 0.6×	333 1.0×	152	3.8k
Angelo Selicorni Italy	29	2.5k 0.9×	1.8k 0.9×	553 0.5×	191 0.5×	206 0.6×	176	3.8k

Countries citing papers authored by Ian A. Glass

Since Specialization

Citations

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

Fields of papers citing papers by Ian A. Glass

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ian A. Glass. 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 Ian A. Glass. The network helps show where Ian A. Glass may publish in the future.

Co-authorship network of co-authors of Ian A. Glass

This figure shows the co-authorship network connecting the top 25 collaborators of Ian A. Glass. A scholar is included among the top collaborators of Ian A. Glass 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 Ian A. Glass. Ian A. Glass 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

Yang, Ying, Lucas Seninge, Lihao Guo, et al.. (2025). A spatiotemporal and machine-learning platform facilitates the manufacturing of hPSC-derived esophageal mucosa. Developmental Cell. 60(9). 1359–1376.e10. 2 indexed citations

Wang, Danyang, et al.. (2025). Chromosomal instability in human trophoblast stem cells and placentas. Nature Communications. 16(1). 3918–3918. 3 indexed citations

Bhattacharya, Soumyaroop, Gail Deutsch, Ian A. Glass, et al.. (2025). The transcriptional landscape of developing human trisomy 21 lungs. American Journal of Respiratory Cell and Molecular Biology. 74(3). 388–402.

D’Souza, Shane P., Brian A. Upton, Kiara C. Eldred, et al.. (2024). Developmental control of rod number via a light-dependent retrograde pathway from intrinsically photosensitive retinal ganglion cells. Developmental Cell. 59(21). 2897–2911.e6. 2 indexed citations

Garand, Mathieu, et al.. (2024). Differential Regulation of Immune-Related Genes in the Developing Heart. Pediatric Cardiology. 46(2). 442–457. 2 indexed citations

Engel, Abbi L., et al.. (2024). Lipid Nanoparticle-Mediated Delivery of mRNA Into the Mouse and Human Retina and Other Ocular Tissues. Translational Vision Science & Technology. 13(7). 7–7. 9 indexed citations

Frum, Tristan, Peggy P. Hsu, Ansley S. Conchola, et al.. (2023). Opposing roles for TGFβ- and BMP-signaling during nascent alveolar differentiation in the developing human lung. npj Regenerative Medicine. 8(1). 48–48. 6 indexed citations

Yaqubi, Moein, Konstantin Senkevich, Adam MacDonald, et al.. (2023). MerTK is a mediator of alpha-synuclein fibril uptake by human microglia. Brain. 147(2). 427–443. 10 indexed citations

Shen, Minjie, Qiping Dong, Carissa L. Sirois, et al.. (2023). Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway. Nature Communications. 14(1). 3801–3801. 16 indexed citations

10.

Danopoulos, Soula, Gail Deutsch, Ian A. Glass, et al.. (2022). Hedgehog Signaling Pathway Orchestrates Human Lung Branching Morphogenesis. International Journal of Molecular Sciences. 23(9). 5265–5265. 9 indexed citations

11.

Domcke, Silvia, Andrew J. Hill, Riza M. Daza, et al.. (2020). A human cell atlas of fetal chromatin accessibility. Science. 370(6518). 230 indexed citations

12.

Cao, Junyue, Diana R. O’Day, Hannah A. Pliner, et al.. (2020). A human cell atlas of fetal gene expression. Science. 370(6518). 383 indexed citations breakdown →

13.

Holloway, Emily M., Joshua H. Wu, Michael Czerwinski, et al.. (2020). Differentiation of Human Intestinal Organoids with Endogenous Vascular Endothelial Cells. Developmental Cell. 54(4). 516–528.e7. 87 indexed citations

14.

Roy, Achira, Mei Deng, James W. MacDonald, et al.. (2019). PI3K-Yap activity drives cortical gyrification and hydrocephalus in mice. eLife. 8. 33 indexed citations

15.

Brooks, Brian P., Wadih M. Zein, A. Thompson, et al.. (2018). Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single Center. Ophthalmology. 125(12). 1937–1952. 41 indexed citations

16.

Hoshino, Akina, Rinki Ratnapriya, Matthew J. Brooks, et al.. (2017). Molecular Anatomy of the Developing Human Retina. Developmental Cell. 43(6). 763–779.e4. 169 indexed citations

17.

Bennett, Craig L., et al.. (2005). Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures. Neurogenetics. 6(3). 143–149. 28 indexed citations

18.

Hoeve, James N. Ver, et al.. (2004). Spondylometaphyseal dysplasia with cone‐rod dystrophy. American Journal of Medical Genetics Part A. 129A(3). 265–276. 15 indexed citations

19.

Cross, I, et al.. (2002). Trisomy of the short stature homeobox‐containing gene (SHOX), resulting from a duplication‐deletion of the X chromosome. Clinical Endocrinology. 56(5). 671–675. 21 indexed citations

20.

Glass, Ian A., Adrian Trenholme, Lindsay Mildenhall, Richard J. Bailey, & Philip D. Cotter. (2000). Mild phenotype in two siblings with distal monosomy 12p13.31→pter. Clinical Genetics. 57(5). 401–405. 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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