Pablo V. Gejman

8.5k total citations · 1 hit paper
58 papers, 3.4k citations indexed

About

Pablo V. Gejman is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Pablo V. Gejman has authored 58 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 24 papers in Genetics and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Pablo V. Gejman's work include Genetic Associations and Epidemiology (13 papers), Genomic variations and chromosomal abnormalities (10 papers) and Receptor Mechanisms and Signaling (10 papers). Pablo V. Gejman is often cited by papers focused on Genetic Associations and Epidemiology (13 papers), Genomic variations and chromosomal abnormalities (10 papers) and Receptor Mechanisms and Signaling (10 papers). Pablo V. Gejman collaborates with scholars based in United States, Argentina and Sweden. Pablo V. Gejman's co-authors include Eitan Friedman, Lee S. Weinstein, Allen M. Spiegel, Alan R. Sanders, Andrew Shenker, Maria J. Merino, Jubao Duan, Anibal Cravchik, Daniel P. Cardinali and Kenneth S. Kendler and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and JAMA.

In The Last Decade

Pablo V. Gejman

57 papers receiving 3.3k 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.

Activating Mutations of the Stimulatory G Protein in the McCune–Albright Syndrome

1991 1.2k citations Lee S. Weinstein, Andrew Shenker et al. New England Journal of Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Pablo V. Gejman United States	28	1.5k	980	652	507	440	58	3.4k
Lodewijk A. Sandkuijl Netherlands	44	3.9k 2.6×	1.9k 2.0×	354 0.5×	755 1.5×	529 1.2×	94	7.7k
Kathrin Saar Germany	32	2.4k 1.6×	1.1k 1.1×	108 0.2×	600 1.2×	434 1.0×	73	4.1k
Yiping Shen United States	36	2.8k 1.9×	2.6k 2.7×	197 0.3×	582 1.1×	220 0.5×	195	5.6k
Bert B.A. de Vries Netherlands	39	3.6k 2.4×	5.1k 5.2×	255 0.4×	305 0.6×	169 0.4×	114	7.4k
J.R.M. Cruysberg Netherlands	29	1.2k 0.8×	478 0.5×	344 0.5×	259 0.5×	157 0.4×	113	3.5k
Thomas Eggermann Germany	44	4.2k 2.8×	4.5k 4.5×	238 0.4×	292 0.6×	151 0.3×	299	7.0k
Michael Knapp Germany	43	1.9k 1.2×	2.4k 2.5×	142 0.2×	1.1k 2.1×	216 0.5×	147	5.2k
R. Ellen Magenis United States	32	2.0k 1.4×	2.0k 2.1×	177 0.3×	469 0.9×	199 0.5×	71	3.7k
Vera M. Kalscheuer Germany	45	4.4k 2.9×	3.6k 3.7×	144 0.2×	586 1.2×	351 0.8×	152	6.7k
Tania Attié‐Bitach France	42	3.6k 2.4×	2.4k 2.5×	128 0.2×	333 0.7×	212 0.5×	156	6.7k

Countries citing papers authored by Pablo V. Gejman

Since Specialization

Citations

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

Fields of papers citing papers by Pablo V. Gejman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pablo V. Gejman. 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 Pablo V. Gejman. The network helps show where Pablo V. Gejman may publish in the future.

Co-authorship network of co-authors of Pablo V. Gejman

This figure shows the co-authorship network connecting the top 25 collaborators of Pablo V. Gejman. A scholar is included among the top collaborators of Pablo V. Gejman 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 Pablo V. Gejman. Pablo V. Gejman 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

Zhang, Siwei, Winton Moy, Hanwen Zhang, et al.. (2018). Open chromatin dynamics reveals stage-specific transcriptional networks in hiPSC-based neurodevelopmental model. Stem Cell Research. 29. 88–98. 16 indexed citations

Sanders, Alan R., Eugene Drigalenko, Jubao Duan, et al.. (2017). Transcriptome sequencing study implicates immune-related genes differentially expressed in schizophrenia: new data and a meta-analysis. Translational Psychiatry. 7(4). e1093–e1093. 42 indexed citations

Duan, Jubao, Hanwen Zhang, Marc P. Forrest, et al.. (2017). Open Chromatin Dynamics In Ipsc-Derived Neurons And CRISPR/CAS9 Editing of open Chromatin Sequences At The MIR137 Schizophrenia Risk Locus Alters Synapto-Dendritic Architecture. European Neuropsychopharmacology. 27. S429–S430.

Forrest, Marc P., Hanwen Zhang, Winton Moy, et al.. (2017). Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci. Cell stem cell. 21(3). 305–318.e8. 80 indexed citations

Sanders, Alan R., Eden R. Martin, Gary W. Beecham, et al.. (2014). Genome-wide scan demonstrates significant linkage for male sexual orientation. Psychological Medicine. 45(7). 1379–1388. 84 indexed citations

Russell, Theron A., Katherine D. Blizinsky, Derin Cobia, et al.. (2014). A sequence variant in human KALRN impairs protein function and coincides with reduced cortical thickness. Nature Communications. 5(1). 4858–4858. 28 indexed citations

Gejman, Pablo V. & Alan R. Sanders. (2012). La etiología de la esquizofrenia. SHILAP Revista de lepidopterología. 72(3). 227–234. 3 indexed citations

Gejman, Pablo V., Alan R. Sanders, & Jubao Duan. (2010). The Role of Genetics in the Etiology of Schizophrenia. Psychiatric Clinics of North America. 33(1). 35–66. 194 indexed citations

Duan, Jubao, María Martínez, Alan R. Sanders, et al.. (2004). Polymorphisms in the Trace Amine Receptor 4 (TRAR4) Gene on Chromosome 6q23.2 Are Associated with Susceptibility to Schizophrenia. The American Journal of Human Genetics. 75(4). 624–638. 66 indexed citations

10.

Gejman, Pablo V., et al.. (2001). Linkage analysis of schizophrenia to chromosome 15. American Journal of Medical Genetics. 105(8). 789–793. 45 indexed citations

11.

Gejman, Pablo V., et al.. (1998). The sensitivity of denaturing gradient gel electrophoresis: a blinded analysis. PubMed. 382(3-4). 109–114. 21 indexed citations

12.

Warner, Dennis, Pablo V. Gejman, Regina M. Collins, & Lee S. Weinstein. (1997). A Novel Mutation Adjacent to the Switch III Domain of G_sαin a Patient with Pseudohypoparathyroidism. Molecular Endocrinology. 11(11). 1718–1727. 46 indexed citations

13.

Cravchik, Anibal, David R. Sibley, & Pablo V. Gejman. (1996). Functional Analysis of the Human D2 Dopamine Receptor Missense Variants. Journal of Biological Chemistry. 271(42). 26013–26017. 103 indexed citations

14.

Friedman, Eitan, Pablo V. Gejman, George A. Martin, & Frank McCormick. (1993). Nonsense mutations in the C–terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours. Nature Genetics. 5(3). 242–247. 46 indexed citations

15.

Coon, Hilary, Mark Hoff, John Holik, et al.. (1993). C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families. American Journal of Medical Genetics. 48(1). 36–39. 8 indexed citations

16.

Gejman, Pablo V., Lee S. Weinstein, María Martínez, et al.. (1991). Genetic mapping of the Gs-α subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis. Genomics. 9(4). 782–783. 50 indexed citations

17.

Weinstein, Lee S., Andrew Shenker, Pablo V. Gejman, et al.. (1991). Activating Mutations of the Stimulatory G Protein in the McCune–Albright Syndrome. New England Journal of Medicine. 325(24). 1688–1695. 1155 indexed citations breakdown →

18.

Martínez, María, et al.. (1990). Genetic mapping of common diseases: the challenges of manic-depressive illness and schizophrenia. Trends in Genetics. 6(9). 282–286. 16 indexed citations

19.

Cardinali, Daniel P., María I. Vacas, Mónica N. Ritta, & Pablo V. Gejman. (1983). Neurotransmitter-controlled steroid hormone receptors in the central nervous system. Neurochemistry International. 5(2). 185–192. 9 indexed citations

20.

Cardinali, Daniel P., Mónica N. Ritta, & Pablo V. Gejman. (1982). Norepinephrine stimulates testosterone aromatization and inhibits 5α reduction via β-adrenoceptors in rat pineal gland. Molecular and Cellular Endocrinology. 28(2). 199–209. 39 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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