Sara Mole

10.8k citations

147 papers · 7.2k indexed · 1 hit paper · h-index 41

Physiology top 0.2%
- Lysosomal Storage Disorders Research 109
- Calcium signaling and nucleotide metabolism 17
Physiology top 0.2%
- Lysosomal Storage Disorders Research 109
- Calcium signaling and nucleotide metabolism 17
Cell Biology top 0.2%
- Cellular transport and secretion 46
Rheumatology top 1%
- Glycogen Storage Diseases and Myoclonus 19
Endocrinology, Diabetes and Metabolism top 1%
Molecular Biology
- Glycosylation and Glycoproteins Research 29
- RNA regulation and disease 11
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 22
Epidemiology
- Trypanosoma species research and implications 12

Co-authors: Ruth Williams Anna‐Elina Lehesjoki Emily Gardner Susan L. Cotman Alan Tunnacliffe Lois M. Mulligan Catherine S. Healey Laura Papi
Cited by: Physiology Cell Biology
Journals: European Journal of Paediatric Neurology (14 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (12 papers)Human Mutation (8 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Sara Mole

142 papers receiving 7.0k citations

Hit Papers

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Peers

Countries citing papers authored by Sara Mole

Since Specialization

Citations

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

Fields of papers citing papers by Sara Mole

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Sara Mole, 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 Sara Mole Line = papers co-authored together Sara Mole links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The Batten disease protein CLN3 is important for stress granules dynamics and translational activity Journal of Biological Chemistry ·M Bourgeois,C. MacDougall,Aslıhan Zeynep Öz,刑法「改正」阻止実行委員会,Guido Hermey,Rita Giordano,Sara Mole,Tatyana A. Shelkovnikova,Stéphane Lefrançois,Peter J. McCormick,Nicolas Locker	2023	4
2	Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease Human Molecular Genetics ·Sophia-Martha kleine Holthaus,Saúl Herranz-Martín,Giulia Massaro,Mikel Aristorena,Karen Stenning,Michael P. Hughes,Ryea Maswood,泉藤井,Mark Basche,Amna Z. Shah,공여진,Alexander J. Smith,Sara Mole,Rahimin Affandi Abdul Rahim,Robin R. Ali	2019	23
3	Moving towards a new era of genomics in the neuronal ceroid lipofuscinoses Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Elisabeth Butz,Uma Chandrachud,Sara Mole,Susan L. Cotman	2019	40
4	Neuronal ceroid lipofuscinoses Epileptic Disorders ·Dragos A. Nita,Sara Mole,Berge A. Minassian	2016	106
5	Genetics of the neuronal ceroid lipofuscinoses (Batten disease) Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Sara Mole,Susan L. Cotman	2015	228
6	Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Varun Warrier,Shizhong Peng,Sara Mole	2013	92
7	Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage The American Journal of Human Genetics ·Katherine R. Smith,John A. Damiano,Silvana Franceschetti,Stirling Carpenter,Laura Canafoglia,Michela Morbin,Giacomina Rossi,Davide Pareyson,Sara Mole,John F. Staropoli,Katherine B. Sims,Jada Lewis,Wen-Lang Lin,Dennis W. Dickson,Hans‐Henrik M. Dahl,Melanie Bahlo,Samuel F. Berkovic	2012	356
8	Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis The American Journal of Human Genetics ·Lenka Nosková,Viktor Stránecký,Hana Hartmannová,Anna Přistoupilová,Veronika Barešová,Robert Ivánek,Helena Hůlková,Helena Jahnová,Julie van der Zee,John F. Staropoli,Katherine B. Sims,Jaana Tyynelä,Christine Van Broeckhoven,Peter C.G. Nijssen,Sara Mole,M. Elleder,Stanislav Kmoch	2011	10
9	Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses Human Mutation ·Maria Kousi,Anna‐Elina Lehesjoki,Sara Mole	2011	257
10	Deletion of btn 1, an orthologue of CLN 3, increases glycolysis and perturbs amino acidmetabolism in the fission yeast model of Batten disease Molecular BioSystems ·Samantha Ellis,Sandra Codlin,Rebecca L. Haines,Ian J. White,Russell J. Mortishire‐Smith,Sara Mole,Julian L. Griffin	2010	17
11	A 30-year Follow-Up of a Neuronal Ceroid Lipofuscinosis Patient With Mutations in CLN3 and Protracted Disease Course Pediatric Neurology ·L. Åberg,Leena Lauronen,Theresa Horne,Sara Mole,Taina Autti	2009	11
12	Neuronal ceroid lipofuscinoses (NCL) European Journal of Paediatric Neurology ·Sara Mole	2004	3
13	A murine model for juvenile NCL: Gene targeting of mouse CLn3 (vol 66, pg 309, 1999) UCL Discovery (University College London) ·Seung-Kyu,Brent Adkins,JADWIGA ZIEMIECKA,Andriy Lutskiv,Nathalie De Vos,M.H. Breuning,(unknown),Sara Mole,芳弟牛,Hannah M. Mitchison	1999	0
14	Molecular Genetics of the Neuronal Ceroid Lipofuscinoses Epilepsia ·Sara Mole,Mark Gardiner	1999	19
15	Molecular basis of the neuronal ceroid lipofuscinoses: Mutations inCLN1,CLN2,CLN3, andCLN5 Human Mutation ·Sara Mole,Hannah M. Mitchison,Patricia B. Munroe	1999	47
16	Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits (vol 7, pg 291, 1998) UCL Discovery (University College London) ·(unknown),Aasma Yawar,Kiril Borziak,Patricia B. Munroe,Andriy Lutskiv,Yanick J. Crow,(unknown),Robert W. Williams,(unknown),JADWIGA ZIEMIECKA,J.J. Martin,Michel Philippart,(unknown),(unknown),Sara Mole,(unknown),Larry Bafia	1998	1
17	EXTENDING THE GENETIC-MAP OF THE PERICENTROMERIC REGION OF CHROMOSOME-10 UCL Discovery (University College London) ·Emily Gardner,(unknown),Sara Mole,(unknown),(unknown),Laura Papi,(unknown)	1991	1
18	IS THE RET PROTOONCOGENE A CANDIDATE FOR THE MEN2 GENE UCL Discovery (University College London) ·(unknown),Emily Gardner,Sara Mole,Yusuke Nakamura,Laura Papi,(unknown),(unknown)	1991	6
19	Structure and function of SV40 large-T antigen Philosophical transactions of the Royal Society of London. Series B, Biological sciences ·Sara Mole,Julian Gannon,M J Ford,David P. Lane	1987	56
20	Cellular targets for SV40 Large T-antigen Proceedings of the Royal Society of London. Series B, Biological sciences ·David P. Lane,Viesturs Simanis,Dragoș Cosmin Lucian Preda,Jonathan W. Yewdell,Julian Gannon,Sara Mole	1985	24

About Sara Mole

Sara Mole is a scholar working on Physiology, Physiology and Cell Biology, having authored 147 papers that have together received 7.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (109 papers), Cellular transport and secretion (46 papers), Glycosylation and Glycoproteins Research (29 papers), Carbohydrate Chemistry and Synthesis (22 papers), Glycogen Storage Diseases and Myoclonus (19 papers), Calcium signaling and nucleotide metabolism (17 papers), Trypanosoma species research and implications (12 papers) and RNA regulation and disease (11 papers). The work is most often cited by research in Physiology (810 citations), Physiology (4.1k citations) and Cell Biology (2.5k citations). Sara Mole has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Ruth Williams, Anna‐Elina Lehesjoki, Emily Gardner, Susan L. Cotman, Alan Tunnacliffe, Lois M. Mulligan, Catherine S. Healey, Laura Papi, Bruce A.J. Ponder and Margaret A. Ponder. Their work appears in journals such as European Journal of Paediatric Neurology, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Human Mutation, Human Molecular Genetics and Molecular Genetics and Metabolism.

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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