Herbert M. Lachman

9.6k total citations · 2 hit papers
107 papers, 7.4k citations indexed

About

Herbert M. Lachman is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Herbert M. Lachman has authored 107 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 40 papers in Genetics and 23 papers in Cellular and Molecular Neuroscience. Recurrent topics in Herbert M. Lachman's work include Genetics and Neurodevelopmental Disorders (29 papers), Neurotransmitter Receptor Influence on Behavior (16 papers) and Bipolar Disorder and Treatment (16 papers). Herbert M. Lachman is often cited by papers focused on Genetics and Neurodevelopmental Disorders (29 papers), Neurotransmitter Receptor Influence on Behavior (16 papers) and Bipolar Disorder and Treatment (16 papers). Herbert M. Lachman collaborates with scholars based in United States, Czechia and Japan. Herbert M. Lachman's co-authors include Takuya Saito, Demitri F. Papolos, Jan Volavka, Richard M. Weinshilboum, Carol L. Szumlanski, Arthur I. Skoultchi, Robert M. Bilder, Erika Pedrosa, Deyou Zheng and Anthony A. Grace and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Herbert M. Lachman

106 papers receiving 7.2k 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.

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders

1996 1.4k citations Herbert M. Lachman, Demitri F. Papolos et al. profile →
The Catechol-O-Methyltransferase Polymorphism: Relations to the Tonic–Phasic Dopamine Hypothesis and Neuropsychiatric Phenotypes

2004 614 citations Robert M. Bilder, Jan Volavka et al. profile →

Peers

Herbert M. Lachman

GENET

PMH

CMN

Stephen J. Glatt United States

Fabìo Macciardi Italy

Sven Cichon Germany

Douglas Blackwood United Kingdom

Chiara Maria Mazzanti Italy

Peter Holmans United Kingdom

Roel A. Ophoff Netherlands

Wade H. Berrettini United States

Andrea Schmitt Germany

Erik G. Jönsson Sweden

Stephen J. Glatt United States

Herbert M. Lachman

2.2k ×0.7

2.0k ×1.1

GENET

2.4k ×1.4

PMH

1.1k ×0.7

CMN

1.4k ×0.9

Citations per year, relative to Herbert M. Lachman Herbert M. Lachman (= 1×) peers Stephen J. Glatt

Countries citing papers authored by Herbert M. Lachman

Since Specialization

Citations

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

Fields of papers citing papers by Herbert M. Lachman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Herbert M. Lachman. 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 Herbert M. Lachman. The network helps show where Herbert M. Lachman may publish in the future.

Co-authorship network of co-authors of Herbert M. Lachman

This figure shows the co-authorship network connecting the top 25 collaborators of Herbert M. Lachman. A scholar is included among the top collaborators of Herbert M. Lachman 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 Herbert M. Lachman. Herbert M. Lachman 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

Lachman, Herbert M., et al.. (2022). Characterization of cell-cell communication in autistic brains with single-cell transcriptomes. Journal of Neurodevelopmental Disorders. 14(1). 29–29. 8 indexed citations

Li, Jianping, Sean K. Ryan, Herbert M. Lachman, et al.. (2019). Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia. Translational Psychiatry. 9(1). 302–302. 61 indexed citations

Wang, Ping, Dejian Zhao, Herbert M. Lachman, & Deyou Zheng. (2018). Enriched expression of genes associated with autism spectrum disorders in human inhibitory neurons. Translational Psychiatry. 8(1). 57–92. 42 indexed citations

Mokhtari, Ryan, et al.. (2018). Modeling the neuropsychiatric manifestations of Lowe syndrome using induced pluripotent stem cells: defective F-actin polymerization and WAVE-1 expression in neuronal cells. Molecular Autism. 9(1). 44–44. 19 indexed citations

Mokhtari, Ryan & Herbert M. Lachman. (2016). The Major Histocompatibility Complex (MHC) in Schizophrenia: A Review. Journal of Clinical & Cellular Immunology. 7(6). 68 indexed citations

Wang, Ping, Mingyan Lin, Erika Pedrosa, et al.. (2015). CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment. Molecular Autism. 6(1). 112 indexed citations

Lin, Mingyan, Dejian Zhao, Anastasia Hrabovsky, et al.. (2014). Heat Shock Alters the Expression of Schizophrenia and Autism Candidate Genes in an Induced Pluripotent Stem Cell Model of the Human Telencephalon. PLoS ONE. 9(4). e94968–e94968. 39 indexed citations

Pedrosa, Erika, Joseph Locker, & Herbert M. Lachman. (2009). Survey of Schizophrenia and Bipolar Disorder Candidate Genes using Chromatin Immunoprecipitation and Tiled Microarrays (ChIP-chip). Journal of Neurogenetics. 23(3). 341–352. 9 indexed citations

Lachman, Herbert M.. (2008). Copy variations in schizophrenia and bipolar disorder. Cytogenetic and Genome Research. 123(1-4). 27–35. 9 indexed citations

10.

Lachman, Herbert M., Cathy S.J. Fann, Oleg V. Evgrafov, et al.. (2007). Genomewide suggestive linkage of opioid dependence to chromosome 14q. Human Molecular Genetics. 16(11). 1327–1334. 69 indexed citations

11.

Pedrosa, Erika, et al.. (2006). Positive association of schizophrenia to JARID2 gene. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(1). 45–51. 25 indexed citations

12.

Lachman, Herbert M.. (2006). An overview of the genetics of substance use disorders. Current Psychiatry Reports. 8(2). 133–143. 26 indexed citations

13.

Lachman, Herbert M., et al.. (2005). Analysis of polymorphisms in AT‐rich domains of neuregulin 1 gene in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(1). 102–109. 33 indexed citations

14.

Nolan, Karen A., Robert M. Bilder, Herbert M. Lachman, & Jan Volavka. (2004). CatecholO-Methyltransferase Val¹⁵⁸Met Polymorphism in Schizophrenia: Differential Effects of Val and Met Alleles on Cognitive Stability and Flexibility. American Journal of Psychiatry. 161(2). 359–361. 188 indexed citations

15.

Saito, Takuya, Herbert M. Lachman, Tero Hallikainen, et al.. (2002). Analysis of monoamine oxidase A (MAOA) promoter polymorphism in Finnish male alcoholics. Psychiatry Research. 109(2). 113–119. 60 indexed citations

16.

Russ, Mark J., et al.. (2000). Analysis of catechol-O-methyltransferase and 5-hydroxytryptamine transporter polymorphisms in patients at risk for suicide. Psychiatry Research. 93(1). 73–78. 71 indexed citations

17.

Hallikainen, Tero, Herbert M. Lachman, Takuya Saito, et al.. (2000). Lack of association between the functional variant of the catechol-o-methyltransferase (COMT) gene and early-onset alcoholism associated with severe antisocial behavior. American Journal of Medical Genetics. 96(3). 348–352. 52 indexed citations

18.

Lachman, Herbert M., Bernice E. Morrow, Robert J. Shprintzen, et al.. (1996). Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. American Journal of Medical Genetics. 67(5). 468–472. 239 indexed citations

19.

Lachman, Herbert M., et al.. (1993). Alterations in glucocorticoid inducible RNAs in the limbic system of learned helpless rats. Brain Research. 609(1-2). 110–116. 29 indexed citations

20.

Papolos, Demitri F., et al.. (1991). Lithium augments pilocarpine-inducedfos gene expression in rat brain. Brain Research. 553(1). 117–122. 32 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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