Lauren A. Weiss

19.6k total citations · 2 hit papers
69 papers, 5.2k citations indexed

About

Lauren A. Weiss is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Lauren A. Weiss has authored 69 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 23 papers in Molecular Biology and 22 papers in Cognitive Neuroscience. Recurrent topics in Lauren A. Weiss's work include Autism Spectrum Disorder Research (22 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Genomic variations and chromosomal abnormalities (15 papers). Lauren A. Weiss is often cited by papers focused on Autism Spectrum Disorder Research (22 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Genomic variations and chromosomal abnormalities (15 papers). Lauren A. Weiss collaborates with scholars based in United States, United Kingdom and France. Lauren A. Weiss's co-authors include Dan E. Arking, Carole Ober, Mark Abney, Hreinn Stefánsson, Elizabeth Barrett‐Connor, Denise von Mühlen, Lin Pan, Edwin H. Cook, Brett S. Abrahams and Rudolph E. Tanzi and has published in prestigious journals such as Nature, New England Journal of Medicine and Neuron.

In The Last Decade

Lauren A. Weiss

67 papers receiving 5.1k citations

Hit Papers

align trajectories sort by overperformance

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.

Association between Microdeletion and Microduplication at 16p11.2 and Autism

2008 1.1k citations Lauren A. Weiss et al. profile →
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

2013 495 citations Lauren A. Weiss et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lauren A. Weiss United States	34	2.8k	2.1k	1.8k	410	365	69	5.2k
Joussef Hayek Italy	42	3.6k 1.3×	3.2k 1.5×	1.9k 1.1×	354 0.9×	272 0.7×	181	6.0k
Rita M. Cantor United States	45	3.4k 1.2×	2.8k 1.3×	2.6k 1.4×	499 1.2×	468 1.3×	90	7.2k
Thierry Bienvenu France	38	3.2k 1.1×	2.4k 1.2×	944 0.5×	223 0.5×	379 1.0×	200	5.6k
Nicole Tartaglia United States	36	2.9k 1.0×	1.9k 0.9×	1.5k 0.8×	143 0.3×	499 1.4×	99	4.6k
M. E. Suzanne Lewis Canada	33	1.3k 0.5×	1.5k 0.7×	910 0.5×	371 0.9×	1.0k 2.8×	110	4.2k
Mark E.S. Bailey United Kingdom	37	2.3k 0.8×	1.5k 0.7×	1.2k 0.7×	753 1.8×	433 1.2×	82	4.7k
Allison E. Ashley‐Koch United States	48	1.8k 0.6×	2.2k 1.1×	1.6k 0.9×	531 1.3×	1.3k 3.5×	210	8.3k
Hideo Matsuzaki Japan	34	1.1k 0.4×	2.4k 1.2×	1.2k 0.7×	363 0.9×	1.0k 2.8×	125	5.3k
Yann Hérault France	38	1.8k 0.6×	3.0k 1.5×	364 0.2×	439 1.1×	288 0.8×	158	5.8k
Corrado Romano Italy	35	1.4k 0.5×	1.6k 0.8×	603 0.3×	257 0.6×	530 1.5×	197	5.1k

Countries citing papers authored by Lauren A. Weiss

Since Specialization

Citations

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

Fields of papers citing papers by Lauren A. Weiss

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lauren A. Weiss

This figure shows the co-authorship network connecting the top 25 collaborators of Lauren A. Weiss. A scholar is included among the top collaborators of Lauren A. Weiss 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 Lauren A. Weiss. Lauren A. Weiss is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Sandin, Sven, Benjamin Hon Kei Yip, Weiyao Yin, et al.. (2024). Examining Sex Differences in Autism Heritability. JAMA Psychiatry. 81(7). 673–673. 11 indexed citations

Croen, Lisa, Jennifer Ames, Yinge Qian, et al.. (2023). Inflammatory Conditions During Pregnancy and Risk of Autism and Other Neurodevelopmental Disorders. SHILAP Revista de lepidopterología. 4(1). 39–50. 15 indexed citations

Marrus, Natasha, Susan E. Maloney, Benjamin Hon Kei Yip, et al.. (2022). Can the “female protective effect” liability threshold model explain sex differences in autism spectrum disorder?. Neuron. 110(20). 3243–3262. 28 indexed citations

Zhong, Xue, et al.. (2021). Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome Medicine. 13(1). 172–172. 22 indexed citations

Traglia, Michela, Gayle C. Windham, Michelle Pearl, et al.. (2020). Genetic Contributions to Maternal and Neonatal Vitamin D Levels. Genetics. 214(4). 1091–1102. 9 indexed citations

Traglia, Michela, Lisa Croen, Karen L. Jones, et al.. (2018). Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. Genome Medicine. 10(1). 67–67. 23 indexed citations

Rauen, Katherine A., et al.. (2018). RASopathies are associated with a distinct personality profile. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(4). 434–446. 9 indexed citations

Deshpande, Aditi & Lauren A. Weiss. (2018). Recurrent reciprocal copy number variants: Roles and rules in neurodevelopmental disorders. Developmental Neurobiology. 78(5). 519–530. 27 indexed citations

Mitra, Ileena, Alinoë Lavillaureix, Erika Yeh, et al.. (2017). Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders. PLoS Genetics. 13(1). e1006516–e1006516. 34 indexed citations

10.

Palmsten, Kristin, et al.. (2017). Most Frequently Reported Prescription Medications and Supplements in Couples Planning Pregnancy: The LIFE Study. Reproductive Sciences. 25(1). 94–101. 14 indexed citations

11.

Mitra, Ileena, Christine Ladd‐Acosta, Lisa Croen, et al.. (2016). Pleiotropic Mechanisms Indicated for Sex Differences in Autism. PLoS Genetics. 12(11). e1006425–e1006425. 56 indexed citations

12.

Yeh, Erika & Lauren A. Weiss. (2016). If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism. Molecular and Cellular Probes. 30(6). 346–356. 2 indexed citations

13.

Croen, Lisa, Anthony Torres, Martin Kharrazi, et al.. (2013). A Genome-Wide Survey of Transgenerational Genetic Effects in Autism. PLoS ONE. 8(10). e76978–e76978. 42 indexed citations

14.

Yang, Xiaoyong, Ernest T. Lam, Jeremy S. Rabinowitz, et al.. (2013). A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Translational Psychiatry. 3(9). e301–e301. 32 indexed citations

15.

Cheng, Ye, et al.. (2013). An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk. Human Molecular Genetics. 22(14). 2960–2972. 36 indexed citations

16.

Weiss, Lauren A., Shaun Purcell, Kate Lawrence, et al.. (2006). Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome. Human Molecular Genetics. 16(1). 107–113. 25 indexed citations

17.

Weiss, Lauren A., Carole Ober, & Edwin H. Cook. (2006). ITGB3 shows genetic and expression interaction with SLC6A4. Human Genetics. 120(1). 93–100. 35 indexed citations

18.

Weiss, Lauren A., Lucille A. Lester, James E. Gern, et al.. (2005). Variation in ITGB3 Is Associated with Asthma and Sensitization to Mold Allergen in Four Populations. American Journal of Respiratory and Critical Care Medicine. 172(1). 67–73. 38 indexed citations

19.

Weiss, Lauren A., Mark Abney, Edwin H. Cook, & Carole Ober. (2004). Sex-Specific Genetic Architecture of Whole Blood Serotonin Levels. The American Journal of Human Genetics. 76(1). 33–41. 112 indexed citations

20.

Roubenoff, Ronenn, Lauren A. Weiss, Ann Yelmokas McDermott, et al.. (1999). A pilot study of exercise training to reduce trunk fat in adults with HIV-associated fat redistribution. AIDS. 13(11). 1373–1375. 121 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.

Explore authors with similar magnitude of impact