Marisa M. Menold

3.3k total citations
29 papers, 2.0k citations indexed

About

Marisa M. Menold is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Marisa M. Menold has authored 29 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Cognitive Neuroscience and 12 papers in Molecular Biology. Recurrent topics in Marisa M. Menold's work include Autism Spectrum Disorder Research (13 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomic variations and chromosomal abnormalities (7 papers). Marisa M. Menold is often cited by papers focused on Autism Spectrum Disorder Research (13 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomic variations and chromosomal abnormalities (7 papers). Marisa M. Menold collaborates with scholars based in United States, Japan and Finland. Marisa M. Menold's co-authors include S Garrett, John R. Gilbert, Michael L. Cuccaro, Ruth K. Abramson, Chantelle M. Wolpert, G. R. DeLong, H Wright, James R. Broach, Jeffery M. Vance and Allison E. Ashley‐Koch and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Molecular and Cellular Biology and Journal of Cell Science.

In The Last Decade

Marisa M. Menold

29 papers receiving 2.0k citations

Peers

Marisa M. Menold

GENET

CMN

Richard J. Schroer United States

Elena Maestrini Italy

Cindy Skinner United States

Silvia De Rubeis United States

Sabine M. Klauck Germany

Carl Dobkin United States

Luis de la Torre-Ubieta United States

Irina Voineagu Australia

Laurent Villard France

Bernhard Suter United States

Richard J. Schroer United States

Marisa M. Menold

1.3k ×1.2

GENET

795 ×0.8

976 ×1.1

208 ×0.8

CMN

173 ×0.7

Citations per year, relative to Marisa M. Menold Marisa M. Menold (= 1×) peers Richard J. Schroer

Countries citing papers authored by Marisa M. Menold

Since Specialization

Citations

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

Fields of papers citing papers by Marisa M. Menold

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marisa M. Menold

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

Dubash, Adi D., Marisa M. Menold, Thomas Samson, et al.. (2009). Chapter 1 Focal Adhesions: New Angles on an Old Structure. International review of cell and molecular biology. 277. 1–65. 66 indexed citations

Ashley‐Koch, Allison E., Hao Mei, James Jaworski, et al.. (2006). An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABA_A Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder.. Annals of Human Genetics. 70(3). 281–292. 46 indexed citations

Whitehead, Patrice L., Marisa M. Menold, Eden R. Martin, et al.. (2005). Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism. The American Journal of Human Genetics. 77(3). 377–388. 269 indexed citations

Raiford, Kimberly L., Irving C. Allen, Eden R. Martin, et al.. (2003). No association between the APOE gene and autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 125B(1). 57–60. 13 indexed citations

Shao, Yujun, Michael L. Cuccaro, Elizabeth R. Hauser, et al.. (2003). Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes. The American Journal of Human Genetics. 72(3). 539–548. 272 indexed citations

Shao, Yujun, Chantelle M. Wolpert, Kimberly L. Raiford, et al.. (2001). Genomic screen and follow‐up analysis for autistic disorder. American Journal of Medical Genetics. 114(1). 99–105. 189 indexed citations

Menold, Marisa M., Yujun Shao, Chantelle M. Wolpert, et al.. (2001). Association Analysis of Chromosome 15 GABA_AReceptor Subunit Genes in Autistic Disorder. Journal of Neurogenetics. 15(3-4). 245–259. 121 indexed citations

Donnelly, Shannon L., Chantelle M. Wolpert, Marisa M. Menold, et al.. (2000). Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome. American Journal of Medical Genetics. 96(3). 312–316. 52 indexed citations

Wolpert, Chantelle M., Marisa M. Menold, Meredyth P. Bass, et al.. (2000). Three probands with autistic disorder and isodicentric chromosome 15. American Journal of Medical Genetics. 96(3). 365–372. 68 indexed citations

10.

Bass, Meredyth P., Marisa M. Menold, Chantelle M. Wolpert, et al.. (2000). Genetic studies in autistic disorder and chromosome 15. Neurogenetics. 2(4). 219–226. 79 indexed citations

11.

Menold, Marisa M., Meredyth P. Bass, Allison R. Rogala, et al.. (1999). Autistic Disorder and Chromosome 15q11–q13: Construction and Analysis of a BAC/PAC Contig. Genomics. 62(3). 325–331. 22 indexed citations

12.

Ashley‐Koch, Allison E., Chantelle M. Wolpert, Marisa M. Menold, et al.. (1999). Genetic Studies of Autistic Disorder and Chromosome 7. Genomics. 61(3). 227–236. 147 indexed citations

13.

Othmane, Kamel Ben, Marisa M. Menold, Felicia L. Graham, et al.. (1999). Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15. Genomics. 62(3). 344–349. 60 indexed citations

14.

Vance, Jeffery M., Larry H. Yamaoka, P. C. Gaskell, et al.. (1998). Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease. Neurobiology of Aging. 19(1). S39–S42. 44 indexed citations

15.

Menold, Marisa M., Menachem Sadeh, Felicia Lennon, et al.. (1998). Evidence for Genetic Heterogeneity Supports Clinical Differences in Congenital Myasthenic Syndromes. Human Heredity. 48(6). 325–332. 2 indexed citations

16.

Vance, Jeffery M., Marcy C. Speer, Felicia Lennon, et al.. (1997). Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity. Neurogenetics. 1(2). 89–93. 18 indexed citations

17.

Ryan, Kathleen R., et al.. (1994). SMS1, a high-copy suppressor of the yeast mas6 mutant, encodes an essential inner membrane protein required for mitochondrial protein import.. Molecular Biology of the Cell. 5(5). 529–538. 71 indexed citations

18.

Robinson, Lucy C., Marisa M. Menold, S Garrett, & Michael R. Culbertson. (1993). Casein Kinase I-Like Protein Kinases Encoded by YCK1 and YCK2 are Required for Yeast Morphogenesis. Molecular and Cellular Biology. 13(5). 2870–2881. 31 indexed citations

19.

Garrett, S, Marisa M. Menold, & James R. Broach. (1991). The Saccharomyces cerevisiae YAK1 Gene Encodes a Protein Kinase That Is Induced by Arrest Early in the Cell Cycle. Molecular and Cellular Biology. 11(8). 4045–4052. 53 indexed citations

20.

Menold, Marisa M. & Elizabeth A. Repasky. (1984). Heterogeneity of spectrin distribution among avian muscle fiber types. Muscle & Nerve. 7(5). 408–414. 17 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