Marjorie Withers

4.3k total citations
23 papers, 1.6k citations indexed

About

Marjorie Withers is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Marjorie Withers has authored 23 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Plant Science. Recurrent topics in Marjorie Withers's work include Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (9 papers) and Genomics and Rare Diseases (5 papers). Marjorie Withers is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (9 papers) and Genomics and Rare Diseases (5 papers). Marjorie Withers collaborates with scholars based in United States, Türkiye and Canada. Marjorie Withers's co-authors include James R. Lupski, Paweł Stankiewicz, Christine J. Shaw, Sung Sup Park, Lorraine Potocki, Lisa G. Shaffer, Weimin Bi, Virginia Kimonis, Catherine D. Kashork and Anne Summers and has published in prestigious journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and Genome Research.

In The Last Decade

Marjorie Withers

23 papers receiving 1.6k citations

Peers

Countries citing papers authored by Marjorie Withers

Since Specialization

Citations

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

Fields of papers citing papers by Marjorie Withers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marjorie Withers

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

#	Work	Indexed citations
1	Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause Microcephaly 2019 ·Developmental Cell ·Nichole Link, Hyung-Lok Chung, Angad Jolly, Marjorie Withers, Burak Tepe, Benjamin R. Arenkiel, Priya S. Shah, Nevan J. Krogan, Hatip Aydın, Bilgen Bilge Geçkinli, Tülay Tos, Sedat Işıkay, Beyhan Tüysüz, Ganeshwaran H. Mochida, (unknown), Robin D. Clark, Ghayda Mirzaa, James R. Lupski, Hugo J. Bellen	66
2	DVL3 Alleles Resulting in a −1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome 2016 ·The American Journal of Human Genetics ·Janson J. White, Juliana F. Mazzeu, Alexander Hoischen, Yavuz Bayram, Marjorie Withers, Alper Gezdirici, Virginia Kimonis, Marloes Steehouwer, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, Bregje W.M. van Bon, V. Reid Sutton, James R. Lupski, Han G. Brunner, Claudia M.B. Carvalho	69
3	The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy 2015 ·Genetics in Medicine ·Davut Pehli̇van, Christine R. Beck, Yuji Okamoto, Tamar Harel, Zeynep H. Coban Akdemir, Shalini N. Jhangiani, Marjorie Withers, (unknown), Claudia M.B. Carvalho, Dirk Czesnik, Claudia Gonzaga‐Jauregui, Wojciech Wiszniewski, Donna M. Muzny, Richard A. Gibbs, Bernd Rautenstrauß, Michael W. Sereda, James R. Lupski	14
4	Comparative Genomic Analyses of the Human NPHP1 Locus Reveal Complex Genomic Architecture and Its Regional Evolution in Primates 2015 ·PLoS Genetics ·Bo Yuan, Pengfei Liu, (unknown), Christine R. Beck, (unknown), Ian M. Campbell, Tomasz Gambin, (unknown), Marjorie Withers, R. Alan Harris, Jeffrey Rogers, David C. Schwartz, James R. Lupski	15
5	Whole-Exome Sequencing Identifies Homozygous GPR161 Mutation in a Family with Pituitary Stalk Interruption Syndrome 2014 ·The Journal of Clinical Endocrinology & Metabolism ·Ender Karaca, Ramazan Büyükkaya, Davut Pehli̇van, Wu‐Lin Charng, Kürşat Oğuz Yaykaşlı, Yavuz Bayram, Tomasz Gambin, Marjorie Withers, Mehmed M. Atik, İlknur Arslanoğlu, Semih Bolu, Serkan Erdin, (unknown), (unknown), Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, James R. Lupski	60
6	Real-time detection of TDP1 activity using a fluorophore–quencher coupled DNA-biosensor 2013 ·Biosensors and Bioelectronics ·(unknown), Mattia Falconi, Emil L. Kristoffersen, (unknown), (unknown), (unknown), Rikke Frøhlich, (unknown), (unknown), Sissel Juul, Yi‐Ping Ho, Marjorie Withers, James R. Lupski, Jørn Koch, Alessandro Desideri, Birgitta R. Knudsen, Magnus Stougaard	37
7	Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki–Lupski duplication syndrome 2012 ·Human Molecular Genetics ·Zhe Sun, Pengfei Liu, Xueyuan Jia, Marjorie Withers, Jin Li, James R. Lupski, Feng Zhang	15
8	Frequency of Nonallelic Homologous Recombination Is Correlated with Length of Homology: Evidence that Ectopic Synapsis Precedes Ectopic Crossing-Over 2011 ·The American Journal of Human Genetics ·Pengfei Liu, Melanie Lacaria, Feng Zhang, Marjorie Withers, P. J. Hastings, (unknown)	76
9	Increased RPA1 Gene Dosage Affects Genomic Stability Potentially Contributing to 17p13.3 Duplication Syndrome 2011 ·PLoS Genetics ·Emily Outwin, Gillian Carpenter, Weimin Bi, Marjorie Withers, James R. Lupski, Mark O’Driscoll	22
10	Transmembrane activator and CAML interactor (TACI) haploinsufficiency results in B-cell dysfunction in patients with Smith-Magenis syndrome 2011 ·Journal of Allergy and Clinical Immunology ·Javier Chinen, Mónica Martínez‐Gallo, Wenli Gu, Montserrat Cols, Andrea Cerutti, Lin Radigan, Li Zhang, Lorraine Potocki, Marjorie Withers, James R. Lupski, Charlotte Cunningham‐Rundles	20
11	Identification of Uncommon Recurrent Potocki-Lupski Syndrome-Associated Duplications and the Distribution of Rearrangement Types and Mechanisms in PTLS 2010 ·The American Journal of Human Genetics ·Feng Zhang, Lorraine Potocki, Jacinda B. Sampson, Pengfei Liu, Amarilis Sanchez‐Valle, Patricia Robbins‐Furman, (unknown), Patricia G. Wheeler, J. Edward Spence, Campbell K. Brasington, Marjorie Withers, James R. Lupski	74
12	Population Bottlenecks as a Potential Major Shaping Force of Human Genome Architecture 2007 ·PLoS Genetics ·Adrian Gherman, Peter E. Chen, Tanya M. Teslovich, Paweł Stankiewicz, Marjorie Withers, Carl Kashuk, Aravinda Chakravarti, James R. Lupski, David J. Cutler, Nicholas Katsanis	48
13	Mutational and genotype–phenotype correlation analyses in 28 Polish patients with Cornelia de Lange syndrome 2006 ·American Journal of Medical Genetics Part A ·Jiong Yan, Gulam Mustafa Saifi, (unknown), Marjorie Withers, Gabriel A. Bien‐Willner, Janusz Limon, Paweł Stankiewicz, James R. Lupski, Jolanta Wierzba	44
14	Position Effects Due to Chromosome Breakpoints that Map ∼900 Kb Upstream and ∼1.3 Mb Downstream of SOX9 in Two Patients with Campomelic Dysplasia 2005 ·The American Journal of Human Genetics ·Gopalrao V.N. Velagaleti, Gabriel A. Bien‐Willner, Jill K. Northup, Lillian H. Lockhart, (unknown), Syed M. Jalal, Marjorie Withers, James R. Lupski, Paweł Stankiewicz	136
15	Population Bottlenecks as a Potential Major Shaping Force of Human Genome Architecture 2005 ·PLoS Genetics ·Adrian Gherman, Peter E. Chen, Tanya M. Teslovich, Paweł Stankiewicz, Marjorie Withers, Carl Kashuk, Aravinda Chakravarti, James R. Lupski, David J. Cutler, Nicholas Katsanis	1
16	Uncommon Deletions of the Smith-Magenis Syndrome Region Can Be Recurrent When Alternate Low-Copy Repeats Act as Homologous Recombination Substrates 2004 ·The American Journal of Human Genetics ·Christine J. Shaw, Marjorie Withers, James R. Lupski	46
17	Serial segmental duplications during primate evolution result in complex human genome architecture 2004 ·Genome Research ·Paweł Stankiewicz, Christine J. Shaw, Marjorie Withers, Ken Inoue, James R. Lupski	87
18	Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements 2003 ·The American Journal of Human Genetics ·Paweł Stankiewicz, Christine J. Shaw, Jason Dapper, Keiko Wakui, Lisa G. Shaffer, Marjorie Withers, Leah I. Elizondo, Sung Sup Park, James R. Lupski	144
19	Reciprocal Crossovers and a Positional Preference for Strand Exchange in Recombination Events Resulting in Deletion or Duplication of Chromosome 17p11.2 2003 ·The American Journal of Human Genetics ·Weimin Bi, Sung Sup Park, Christine J. Shaw, Marjorie Withers, Pragna I. Patel, James R. Lupski	94
20	Molecular mechanism for duplication 17p11.2— the homologous recombination reciprocal of the Smith-Magenis microdeletion 2000 ·Nature Genetics ·Lorraine Potocki, (unknown), Sung Sup Park, (unknown), Marjorie Withers, Virginia Kimonis, Anne Summers, Wendy S. Meschino, Kwame Anyane‐Yeboa, Catherine D. Kashork, Lisa G. Shaffer, James R. Lupski	263

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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