Jacob Lawrence

19.8k total citations
28 papers, 888 citations indexed

About

Jacob Lawrence is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Jacob Lawrence has authored 28 papers receiving a total of 888 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 9 papers in Psychiatry and Mental health. Recurrent topics in Jacob Lawrence's work include Bipolar Disorder and Treatment (9 papers), Genetic Associations and Epidemiology (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Jacob Lawrence is often cited by papers focused on Bipolar Disorder and Treatment (9 papers), Genetic Associations and Epidemiology (8 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Jacob Lawrence collaborates with scholars based in United Kingdom, United States and Canada. Jacob Lawrence's co-authors include Hugh Gurling, Andrew McQuillin, Nicholas Bass, David Curtis, Khalid Choudhury, Vinita Puri, Pamela Sklar, Srinivasa Thirumalai, Shaun Purcell and Radhika Kandaswamy and has published in prestigious journals such as The Journal of Immunology, American Journal of Psychiatry and Biological Psychiatry.

In The Last Decade

Jacob Lawrence

27 papers receiving 866 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jacob Lawrence United Kingdom	18	416	338	286	141	94	28	888
J E Loth United States	8	488 1.2×	266 0.8×	229 0.8×	65 0.5×	39 0.4×	10	764
Khalid Choudhury United Kingdom	11	171 0.4×	199 0.6×	110 0.4×	49 0.3×	66 0.7×	11	435
Sally Timm Denmark	11	106 0.3×	280 0.8×	130 0.5×	120 0.9×	161 1.7×	16	731
Nirmala Akula United States	19	904 2.2×	603 1.8×	574 2.0×	183 1.3×	181 1.9×	42	1.6k
Brandi Rollins United States	19	317 0.8×	698 2.1×	183 0.6×	196 1.4×	227 2.4×	24	1.1k
M J Arranz United Kingdom	9	262 0.6×	249 0.7×	313 1.1×	202 1.4×	77 0.8×	19	694
Erika Loetscher Switzerland	12	179 0.4×	296 0.9×	154 0.5×	205 1.5×	63 0.7×	13	627
Lilah Toker Israel	16	107 0.3×	307 0.9×	137 0.5×	200 1.4×	98 1.0×	27	757
Renata Leke Brazil	16	64 0.2×	219 0.6×	187 0.7×	349 2.5×	97 1.0×	22	861
Ganggang Peng Taiwan	5	74 0.2×	338 1.0×	62 0.2×	197 1.4×	50 0.5×	10	663

Countries citing papers authored by Jacob Lawrence

Since Specialization

Citations

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

Fields of papers citing papers by Jacob Lawrence

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacob Lawrence

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

Lawrence, Jacob, Richard Pilon, Jocelyn Fournier, et al.. (2012). Evidence of recombination producing allelic diversity in MHC class I Mafa‐B and ‐A alleles in cynomolgus macaques. Tissue Antigens. 79(5). 351–358. 3 indexed citations

Lawrence, Jacob, Richard Pilon, Jocelyn Fournier, et al.. (2012). Identification of 23 novel MHC class I alleles in cynomolgus macaques of Philippine and Philippine/Mauritius origins. Tissue Antigens. 79(4). 306–307. 7 indexed citations

Lydall, Gregory, Nicholas Bass, Andrew McQuillin, et al.. (2011). Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder. Psychiatric Genetics. 21(6). 294–306. 51 indexed citations

Pereira, Ana Carla, Andrew McQuillin, Vinay Puri, et al.. (2011). Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 177–187. 29 indexed citations

Curtis, David, Andrew McQuillin, Nicholas Bass, et al.. (2010). Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. Psychiatric Genetics. 21(1). 1–4. 58 indexed citations

Perlis, Roy H., Jordan W. Smoller, Manuel A. R. Ferreira, et al.. (2009). A Genomewide Association Study of Response to Lithium for Prevention of Recurrence in Bipolar Disorder. American Journal of Psychiatry. 166(6). 718–725. 105 indexed citations

McQuillin, Andrew, Nicholas Bass, A C Pereira, et al.. (2009). No evidence for excess runs of homozygosity in bipolar disorder. Psychiatric Genetics. 19(4). 165–170. 30 indexed citations

Datta, Susmita, Andrew McQuillin, Mie Rizig, et al.. (2008). A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia. Molecular Psychiatry. 15(6). 615–628. 45 indexed citations

Puri, Vinay, Andrew McQuillin, Susmita Datta, et al.. (2008). Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3. European Journal of Human Genetics. 16(10). 1275–1282. 16 indexed citations

10.

Choudhury, Khalid, Andrew McQuillin, Vinay Puri, et al.. (2007). A Genetic Association Study of Chromosome 11q22-24 in Two Different Samples Implicates the FXYD6 Gene, Encoding Phosphohippolin, in Susceptibility to Schizophrenia. The American Journal of Human Genetics. 80(4). 664–672. 31 indexed citations

11.

Kalsi, Gursharan, Andrew McQuillin, Birte Degn, et al.. (2006). Identification of the Slynar Gene (AY070435) and Related Brain Expressed Sequences as a Candidate Gene for Susceptibility to Affective Disorders Through Allelic and Haplotypic Association With Bipolar Disorder on Chromosome 12q24. American Journal of Psychiatry. 163(10). 1767–1776. 11 indexed citations

12.

Rizig, Mie, Andrew McQuillin, Vinay Puri, et al.. (2006). Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G‐protein signaling 4 protein (RGS4). American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(3). 296–300. 27 indexed citations

13.

Puri, Vinay, Andrew McQuillin, Khalid Choudhury, et al.. (2006). Fine Mapping by Genetic Association Implicates the Chromosome 1q23.3 Gene UHMK1, Encoding a Serine/Threonine Protein Kinase, as a Novel Schizophrenia Susceptibility Gene. Biological Psychiatry. 61(7). 873–879. 28 indexed citations

14.

Pimm, Jonathan, Andrew McQuillin, Srinivasa Thirumalai, et al.. (2005). The Epsin 4 Gene on Chromosome 5q, Which Encodes the Clathrin-Associated Protein Enthoprotin, Is Involved in the Genetic Susceptibility to Schizophrenia. The American Journal of Human Genetics. 76(5). 902–907. 52 indexed citations

15.

Blaveri, Ekaterini, Gursharan Kalsi, Jacob Lawrence, et al.. (2001). Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1). European Journal of Human Genetics. 9(6). 469–472. 25 indexed citations

16.

Gurling, Hugh, David Curtis, G. Kalsi, et al.. (2000). Genome wide linkage anlaysis supports the presence of two separate susceptibility loci on chromosome 1q32 for biopolar disorder and 1q21-22.3 for schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 96(4). 1 indexed citations

17.

McQuillin, Andrew, et al.. (1999). Adjacent genetic markers on chromosome 11p15.5 at or near the tyrosine hydroxylase locus that show population linkage disequilibrium with each other do not show allelic association with bipolar affective disorder. Psychological Medicine. 29(6). 1449–1454. 8 indexed citations

18.

Vincent, John B., Mario Masellis, Jacob Lawrence, et al.. (1999). Genetic Association Analysis of Serotonin System Genes in Bipolar Affective Disorder. American Journal of Psychiatry. 156(1). 136–138. 67 indexed citations

19.

Turner, Adrian, Jacob Lawrence, Andrew C. H. Chen, Christopher L. Cook, & Hugh Gurling. (1997). Frequency of the A1/A2 alleles of the D2 dopamine receptor (DRD2) gene in a British, Caucasian control group screened to exclude alcoholism and heavy drinking. Addiction Biology. 2(2). 207–213. 10 indexed citations

20.

Hodges, J. R. & Jacob Lawrence. (1971). A comparative study of the laboratory diagnosis of gonorrhea.. PubMed. 8(1). 17–20. 2 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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