Mahim Jain

6.3k total citations · 1 hit paper
36 papers, 1.3k citations indexed

About

Mahim Jain is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mahim Jain has authored 36 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 16 papers in Genetics and 5 papers in Surgery. Recurrent topics in Mahim Jain's work include Connective tissue disorders research (8 papers), Congenital limb and hand anomalies (3 papers) and RNA regulation and disease (3 papers). Mahim Jain is often cited by papers focused on Connective tissue disorders research (8 papers), Congenital limb and hand anomalies (3 papers) and RNA regulation and disease (3 papers). Mahim Jain collaborates with scholars based in United States, Canada and Germany. Mahim Jain's co-authors include Pushpa S. Kalra, Shuye Pu, S. P. Kalra, Atul R. Chopra, Lindsay C. Burrage, V. Reid Sutton, David D. Moore, Dianna M. Milewicz, Juan C. Bournat and Bokai Zhu and has published in prestigious journals such as Cell, Journal of Clinical Investigation and Neuron.

In The Last Decade

Mahim Jain

34 papers receiving 1.3k citations

Hit Papers

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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.

Asprosin, a Fasting-Induced Glucogenic Protein Hormone

2016 382 citations Mahim Jain, V. Reid Sutton et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Mahim Jain	481	337	282	258	232	36	1.3k
Carmencita Pilapil	544 1.1×	211 0.6×	277 1.0×	250 1.0×	120 0.5×	33	1.7k
Juxue Li	559 1.2×	92 0.3×	444 1.6×	453 1.8×	74 0.3×	36	1.7k
Fang Cai	545 1.1×	208 0.6×	501 1.8×	80 0.3×	146 0.6×	51	1.8k
Jie Deng	688 1.4×	377 1.1×	99 0.4×	116 0.4×	186 0.8×	42	1.5k
Jeannie F Todd	524 1.1×	113 0.3×	184 0.7×	563 2.2×	142 0.6×	46	1.8k
Theodore P. Braun	577 1.2×	57 0.2×	472 1.7×	149 0.6×	59 0.3×	45	1.5k
Yizhe Tang	625 1.3×	143 0.4×	428 1.5×	371 1.4×	62 0.3×	23	1.5k
Raffaella Spinazzi	262 0.5×	42 0.1×	285 1.0×	596 2.3×	261 1.1×	41	1.3k
Maria Vrontakis	461 1.0×	75 0.2×	105 0.4×	254 1.0×	63 0.3×	33	1.4k
Satoru Takahashi	382 0.8×	281 0.8×	164 0.6×	34 0.1×	128 0.6×	95	1.1k

Countries citing papers authored by Mahim Jain

Since Specialization

Citations

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

Fields of papers citing papers by Mahim Jain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mahim Jain

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

Jain, Mahim, et al.. (2025). High clinical burden of classical homocystinuria in the United States: a retrospective analysis. Orphanet Journal of Rare Diseases. 20(1). 37–37.

Jain, Mahim, et al.. (2024). Estimating prevalence of classical homocystinuria in the United States using Optum's de-identified market clarity data. Molecular Genetics and Metabolism Reports. 40. 101101–101101.

Jain, Mahim, et al.. (2024). Hereditary Connective Tissue Diseases and Risk of Post-Acute SARS-CoV-2. Viruses. 16(3). 461–461. 1 indexed citations

Blesson, Alyssa, et al.. (2023). The diagnostic odyssey of a patient with dihydropyrimidinase deficiency: a case report and review of the literature. Molecular Case Studies. 9(4). a006319–a006319. 1 indexed citations

Jain, Mahim, et al.. (2021). Caudamins, a new subclass of protein hormones. Trends in Endocrinology and Metabolism. 32(12). 1007–1014. 9 indexed citations

Murdock, David R., Hongzheng Dai, Lindsay C. Burrage, et al.. (2020). Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing. Journal of Clinical Investigation. 131(1). 93 indexed citations

Lee, Eun Jin, Mahim Jain, & Stella Alimperti. (2020). Bone Microvasculature: Stimulus for Tissue Function and Regeneration. Tissue Engineering Part B Reviews. 27(4). 313–329. 45 indexed citations

Nguyen, Thien, Kunwei Wu, Yan Li, et al.. (2020). A Cluster of Autism-Associated Variants on X-Linked NLGN4X Functionally Resemble NLGN4Y. Neuron. 106(5). 759–768.e7. 60 indexed citations

Chen, Shan, Mahim Jain, Shalini N. Jhangiani, et al.. (2019). Genetic Burden Contributing to Extremely Low or High Bone Mineral Density in a Senior Male Population From the Osteoporotic Fractures in Men Study (MrOS). JBMR Plus. 4(3). e10335–e10335. 1 indexed citations

10.

Jin, Zixue, Lindsay C. Burrage, Ming‐Ming Jiang, et al.. (2018). Whole‐Exome Sequencing Identifies an Intronic Cryptic Splice Site in SERPINF1 Causing Osteogenesis Imperfecta Type VI. JBMR Plus. 2(4). 235–239. 3 indexed citations

11.

Emrick, Lisa, Jill A. Rosenfeld, Seema R. Lalani, et al.. (2018). Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrum. Genetics in Medicine. 21(7). 1652–1656. 11 indexed citations

12.

Machol, Keren, Mahim Jain, Mohammed Almannai, et al.. (2016). Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies. American Journal of Medical Genetics Part A. 173(3). 733–739. 8 indexed citations

13.

Boone, Philip M., Bo Yuan, Shen Gu, et al.. (2015). Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death. Molecular Genetics & Genomic Medicine. 4(1). 77–94. 25 indexed citations

14.

Jain, Mahim, David Cuthbertson, Deborah Krakow, et al.. (2015). Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta. Genetics in Medicine. 18(6). 570–576. 31 indexed citations

15.

Jain, Mahim, et al.. (2015). Catel–Manzke syndrome: Further delineation of the phenotype associated with pathogenic variants in TGDS. SHILAP Revista de lepidopterología. 4. 89–91. 7 indexed citations

16.

Burrage, Lindsay C., et al.. (2014). Sodium phenylbutyrate decreases plasma branched-chain amino acids in patients with urea cycle disorders. Molecular Genetics and Metabolism. 113(1-2). 131–135. 49 indexed citations

17.

Klopocki, Eva, Silke B. Lohan, Francesco Brancati, et al.. (2010). Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis. The American Journal of Human Genetics. 88(1). 70–75. 67 indexed citations

18.

Wallis, Deeann, Mauricio Arcos‐Burgos, Mahim Jain, et al.. (2009). Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate. ADHD Attention Deficit and Hyperactivity Disorders. 1(1). 19–24. 17 indexed citations

19.

Solomon, Benjamin D., Felicitas Lacbawan, Mahim Jain, et al.. (2009). A novel SIX3 mutation segregates with holoprosencephaly in a large family. American Journal of Medical Genetics Part A. 149A(5). 919–925. 32 indexed citations

20.

Jain, Mahim & David D. Weaver. (2004). Severe lower limb defects in exstrophy of the cloaca. American Journal of Medical Genetics Part A. 128A(3). 320–324. 14 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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