Nancy A. Jenkins

8.8k citations

21 papers · 7.1k indexed · 4 hit papers · h-index 17

Pathology and Forensic Medicine top 0.5%
Cancer Research top 1%
Cell Biology top 1%
- Microtubule and mitosis dynamics 3
- melanin and skin pigmentation 2
- Cellular transport and secretion 2
Molecular Biology top 2%
- RNA Research and Splicing 4
- TGF-β signaling in diseases 3
- Muscle Physiology and Disorders 2
- Congenital heart defects research 2
- Ubiquitin and proteasome pathways 2
Oncology top 2%

Co-authors: N G Copeland Judy E. Garber Mary Kay Lescoe Michael Kane Manchanahalli R. Satyanarayana Rao Richard D. Kolodner Richard Fishel Neal G. Copeland
Cited by: Pathology and Forensic Medicine Cancer Research Cell Biology
Partner nations: United States Germany Russia

In The Last Decade

Nancy A. Jenkins

21 papers receiving 7.0k citations

Hit Papers

align trajectories log scale

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.

1996 Familial Alzheimer's Disease–Linked Presenilin 1 Variants Elevate Aβ1–42/1–40 Ratio In Vitro and In Vivo
1994 Limb alterations in brachypodism mice due to mutations in a new member of the TGFβ-superfamily
1993 The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
1990 Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel alleles

Peers

Countries citing papers authored by Nancy A. Jenkins

Since Specialization

Citations

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

Fields of papers citing papers by Nancy A. Jenkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Nancy A. Jenkins, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nancy A. Jenkins Line = papers co-authored together Nancy A. Jenkins links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Bcl11a (Ctip1) Controls Migration of Cortical Projection Neurons through Regulation of Sema3c Christoph Wiegreffe,Ruth Simon,Katharina Peschkes,Carolin Kling,Michael Strehle,Jin Cheng,Swathi Srivatsa,Pentao Liu,Nancy A. Jenkins,N G Copeland,Victor Tarabykin,Stefan Britsch	2015	81
2	The Paralemmin Protein Family: Identification of Paralemmin-2, an Isoform Differentially Spliced to AKAP2/AKAP-KL, and of Palmdelphin, a More Distant Cytosolic Relative Bin Hu,Neal G. Copeland,Debra J. Gilbert,Nancy A. Jenkins,Manfred W. Kilimann	2001	30
3	Direct interaction of microtubule- and actin-based transport motors Jian‐Dong Huang,Scott T. Brady,Bruce W. Richards,David Stenoien,James H. Resau,N G Copeland,Nancy A. Jenkins	1999	274
4	Genetic mapping of the galanin-GMAP (Galn) gene to mouse Chromosome 19 Letícia da Cunha Guida,Philippa Charlton,Debra J. Gilbert,Nancy A. Jenkins,Neal G. Copeland,Robert D. Nicholls	1998	3
5	Normal function of the transcription factor NFAT1 in wasted mice. Chromosome localization of NFAT1 gene Chun Huai Luo,Neal G. Copeland,Nancy A. Jenkins,Susanne Edelhoff,Christine M. Distèche,Patrick G. Hogan,Anjana Rao	1996	7
6	Familial Alzheimer's Disease–Linked Presenilin 1 Variants Elevate Aβ1–42/1–40 Ratio In Vitro and In Vivobreakdown → David Borchelt,Gopal Thinakaran,Christopher B. Eckman,Michael K. Lee,Frances Davenport,Tamara Ratovitsky,Cristian-Mihail Prada,Grace Kim,Sophia Seekins,Debra Yager,Hilda H. Slunt,Rong Wang,Mary Seeger,Allan I. Levey,Sam Gandy,Neal G. Copeland,Nancy A. Jenkins,Donald L. Price,Steven G. Younkin,Sangram S. Sisodia	1996	1224
7	Growth/Differentiation Factor-10: A New Member of the Transforming Growth Factor-β Superfamily Related to Bone Morphogenetic Protein-3 Noreen S. Cunningham,Nancy A. Jenkins,Debra J. Gilbert,Neal G. Copeland,A. Hari Reddi,Se‐Jin Lee	1995	86
8	Receptor tyrosine kinase specific for the skeletal muscle lineage: Expression in embryonic muscle, at the neuromuscular junction, and after injury David M. Valenzuela,Trevor N. Stitt,Peter S. DiStefano,Eduardo Rojas,Karen Mattsson,Debra Compton,Lorna Nuñez,John S. Park,Jennifer Stark,David R. Gies,Susan E. Thomas,Michelle M. Le Beau,Anthony A. Fernald,Neal G. Copeland,Nancy A. Jenkins,Steven J. Burden,David J. Glass,George D. Yancopoulos	1995	345
9	Interspecific Backcrosses Provide an Important New Tool for Centromere Mapping of Mouse Chromosomes Jeffrey D. Ceci,Yoichi Matsuda,Janet M. Grubber,Nancy A. Jenkins,Neal G. Copeland,Verne M. Chapman	1994	11
10	Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences Eirı́kur Steingrı́msson,Karen J. Moore,M. Lynn Lamoreux,A.R. Ferré-D′Amaré,S.K. Burley,Debra C. Sanders Zimring,Loren C. Skow,Colin A. Hodgkinson,Heinz Arnheiter,N G Copeland,Nancy A. Jenkins	1994	424
11	Limb alterations in brachypodism mice due to mutations in a new member of the TGFβ-superfamilybreakdown → Elaine E. Storm,Thanh V. Huynh,Neal G. Copeland,Nancy A. Jenkins,David M. Kingsley,S. Mark Lee	1994	703
12	The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancerbreakdown → Richard Fishel,Mary Kay Lescoe,Manchanahalli R. Satyanarayana Rao,N G Copeland,Nancy A. Jenkins,Judy E. Garber,Michael Kane,Richard D. Kolodner	1993	2259
13	Chromosomal Localization of Mouse Bullous Pemphigoid Antigens, BPAG1 and BPAG2: Identification of a New Region of Homology between Mouse and Human Chromosomes Neal G. Copeland,Debra J. Gilbert,Kehua Li,Daisuke Sawamura,George J. Giudice,Mon-Li Chu,Nancy A. Jenkins,Jouni Uitto	1993	16
14	GHRH receptor of little mice contains a missense mutation in the extracellular domain that disrupts receptor function Paul A. Godfrey,Jason O. Rahal,Wesley G. Beamer,Neal G. Copeland,Nancy A. Jenkins,Kelly E. Mayo	1993	319
15	Localization of a Novel Natural Killer Triggering Receptor Locus to Human Chromosome 3p23-p21 and Mouse Chromosome 9 Howard A. Young,Nancy A. Jenkins,N G Copeland,Stephanie L. Simek,Michael I. Lerman,Bert Zbar,G.M. Glenn,John R. Ortaldo,Stephen K. Anderson	1993	7
16	The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGFβ superfamily David M. Kingsley,Adrienne E. Bland,Janet M. Grubber,Paul C. Marker,Liane B. Russell,Neal G. Copeland,Nancy A. Jenkins	1992	394
17	Nidogen/entactin (Nid) maps to the proximal end of mouse chromosome 13 linked to beige (bg) and identifies a new region of homology between mouse and human chromosomes Nancy A. Jenkins,Monica J. Justice,Debra J. Gilbert,Mon-Li Chu,Neal G. Copeland	1991	18
18	Genomic organization and chromosomal mapping of the mouse P-cadherin gene Masayuki Hatta,Seiji Miyatani,Neal G. Copeland,Debra J. Gilbert,Nancy A. Jenkins,Masatoshi Takeichi	1991	57
19	Sequence homology shared by neurofibromatosis type-1 gene and IRA-1 and IRA-2 negative regulators of the RAS cyclic AMP pathway Arthur M. Buchberg,Linda S. Cleveland,Nancy A. Jenkins,Neal G. Copeland	1990	174
20	Mast cell growth factor maps near the steel locus on mouse chromosome 10 and is deleted in a number of steel allelesbreakdown → Neal G. Copeland,Debra J. Gilbert,Brian C. Cho,Peter Donovan,Nancy A. Jenkins,David Cosman,Dirk Anderson,Stewart D. Lyman,Douglas E. Williams	1990	535

About Nancy A. Jenkins

Nancy A. Jenkins is a scholar working on Cell Biology, Developmental Neuroscience and Molecular Biology, having authored 21 papers that have together received 7.1k indexed citations. Recurring topics across this work include RNA Research and Splicing (4 papers), TGF-β signaling in diseases (3 papers), Microtubule and mitosis dynamics (3 papers), Muscle Physiology and Disorders (2 papers), melanin and skin pigmentation (2 papers), Cellular transport and secretion (2 papers), Congenital heart defects research (2 papers) and Ubiquitin and proteasome pathways (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (2.0k citations), Cancer Research (1.1k citations) and Cell Biology (1.1k citations). Nancy A. Jenkins has collaborated with scholars based in United States, Germany and Russia. Frequent co-authors include N G Copeland, Judy E. Garber, Mary Kay Lescoe, Michael Kane, Manchanahalli R. Satyanarayana Rao, Richard D. Kolodner, Richard Fishel, Neal G. Copeland, Neal G. Copeland and Thanh V. Huynh.

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