Winnie Xin

3.3k citations

29 papers · 1.2k indexed · h-index 18

Neurology top 5%
- Amyotrophic Lateral Sclerosis Research 5
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 4
- Genomics and Rare Diseases 2
Cell Biology top 5%
- Cellular transport and secretion 6
Physiology top 10%
- Lysosomal Storage Disorders Research 13
- Calcium signaling and nucleotide metabolism 4
Neurology top 10%
- Amyotrophic Lateral Sclerosis Research 5
Molecular Biology
- Mitochondrial Function and Pathology 3
- Glycosylation and Glycoproteins Research 2

Co-authors: Katherine B. Sims Michael Feiss Hiroko Kishikawa David M. Wu Robert H. Brown Yiping Shen A. John Iafrate Rebecca D. Folkerth
Cited by: Neurology Genetics Cell Biology
Journals: Molecular Genetics and Metabolism (3 papers)Journal of Molecular Biology (2 papers)PLoS ONE (2 papers)
Partner nations: United States Argentina Sweden

In The Last Decade

Winnie Xin

29 papers receiving 1.1k citations

Peers

Countries citing papers authored by Winnie Xin

Since Specialization

Citations

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

Fields of papers citing papers by Winnie Xin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Prenatal Testing for Variants in Genes Associated with Hereditary Cancer Risk Journal of Molecular Diagnostics ·Alyce Ferguson,Rodrigo Lima Carvalho,Hui Zhu,Zhaoqing Zhou,Winnie Xin,Hector Morales Corrales,Zena Wolf,Natalia T. Leach	2024	2
2	Identification of Fabry Disease in a Tertiary Referral Cohort of Patients with Hypertrophic Cardiomyopathy The American Journal of Medicine ·Martin S. Maron,Winnie Xin,Katherine B. Sims,TJ Coderre,Tammy S. Haas,Ethan J. Rowin,Robert J. Desnick,Barry J. Maron	2017	33
3	Identification and characterization of a novel DGAT1 missense mutation associated with congenital diarrhea Journal of Lipid Research ·Nina L. Gluchowski,Chandramohan Chitraju,Joseph A. Picoraro,Niklas Mejhert,Shirly Pinto,Winnie Xin,Daniel Kamin,Harland S. Winter,Wendy K. Chung,Tobias C. Walther,Robert V. Farese	2017	39
4	Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis Molecular Genetics and Metabolism ·Michael Fietz,Moeenaldeen AlSayed,Derek Burke,Jessica Cohen‐Pfeffer,Jonathan D. Cooper,Lenka Dvořáková,Roberto Giugliani,Emanuela Izzo,Helena Jahnová,Zoltán Lukács,Sara Mole,Inés Noher de Halac,David A. Pearce,Helena Poupětová,Angela Schulz,Nicola Specchio,Winnie Xin,Nicole L. Miller	2016	67
5	The neuronal ceroid lipofuscinoses program: A translational research experience in Argentina Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·KrishanL Chachra,菊地原靖孝,Norberto Guelbert,Patricia Pons,Bartłomiej Krawczyk,Xiaochuan Yu,R.Valigi Rvaligi,Katherine B. Sims,Winnie Xin,Peter Bentzen,Inés Noher de Halac	2015	18
6	NovelLIPAmutations in Mexican siblings with lysosomal acid lipase deficiency World Journal of Gastroenterology ·Farnaz Fekri,Chi-Keung,Winnie Xin,Kendrick A. Goss,Vikramjit Singh Parmar,Andre Pompe,Raúl E. Piña-Aguilar	2015	13
7	Novel recruitment strategy to enrich forLRRK2mutation carriers Molecular Genetics & Genomic Medicine ·Tatiana Foroud,Danielle Smith,吕尧,Samantha Moldan,Cheryl Halter,Leah Wetherill,Katherine B. Sims,Winnie Xin,Vanessa Arnedo,Shirley Lasch,Kenneth Marek,(unknown)	2015	12
8	Correction: Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families PLoS ONE ·Milen Velinov,Natalia Dolzhanskaya,Michael Gonzalez,Eric Powell,Ioanna Konidari,William Hulme,John F. Staropoli,Winnie Xin,G. Y. Wen,Zongqi Han,Jessica G Santos,Katherine B. Sims,W. Ted Brown,E. Eisenhardt	2012	7
9	Neuronal ceroid lipofuscinosis type CLN2: A new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South America Gene ·KrishanL Chachra,R. Schneppenheim,Winnie Xin,Katherine B. Sims,Norberto Guelbert,Peter Bentzen,Patricia Pons,Mateng Si,M. Troncoso,Agra Utari Dewi,David A. Pearce,Raquel Dodelson de Kremer,Bartłomiej Krawczyk,Inés Noher de Halac	2012	34
10	SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: A United States clinical testing lab experience Amyotrophic Lateral Sclerosis ·Jeffrey A. Brown,Maki Shindo,John F. Staropoli,H. Mauriello,А В Зотя,Xin Feng,Zongqi Han,Yi Cao,bin Ishak Muhamad Syukri,Winnie Xin,Thomas E. Mullen,Katherine B. Sims	2012	45
11	A Homozygous Mutation in KCTD7 Links Neuronal Ceroid Lipofuscinosis to the Ubiquitin-Proteasome System The American Journal of Human Genetics ·John F. Staropoli,Amel Karaa,Elaine T. Lim,Andrew Kirby,K Summer,Stephen G. Romansky,سمیه رسولی ابراهیمی فرد,Jessica G Santos,Zongqi Han,Winnie Xin,Marcy E. MacDonald,José E. Abdenur,Mark J. Daly,Katherine B. Sims,Susan L. Cotman	2012	84
12	An atypical case of neuronal ceroid lipofuscinosis with co-inheritance of a variably penetrant POLG1mutation BMC Medical Genetics ·John F. Staropoli,Winnie Xin,Zongqi Han,Susan L. Cotman,Katherine B. Sims	2012	14
13	Ribonuclease 4 protects neuron degeneration by promoting angiogenesis, neurogenesis, and neuronal survival under stress Angiogenesis ·Shuping Li,Jinghao Sheng,Jamie K. Hu,Wenhao Yu,Hiroko Kishikawa,Miaofen G. Hu,Kaori Shima,David M. Wu,Zhengping Xu,Winnie Xin,Katherine B. Sims,John E. Landers,Robert H. Brown,Guo-fu Hu	2012	47
14	Mutational spectrum of theNF2gene: a meta-analysis of 12 years of research and diagnostic laboratory findings Human Mutation ·Iris Ahronowitz,Winnie Xin,X.Y. Wang,Katherine B. Sims,Mia MacCollin,Fabio P. Nunes	2006	75
15	Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders ·Peter M. Andersen,Katherine B. Sims,Winnie Xin,X.Y. Wang,Gilmore O’Neill,John Ravits,Erik P. Pioro,Yadollah Harati,Richard Brower,何明月,Katsuhiko Yamakawa,William Seltzer,Michael A. Boss,Robert H. Brown	2003	215
16	Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes Amyotrophic Lateral Sclerosis ·Peter M. Andersen,Katherine B. Sims,Winnie Xin,X.Y. Wang,Gilmore O’Neill,John Ravits,Erik P. Pioro,Yadollah Harati,Richard Brower,何明月,Katsuhiko Yamakawa,William Seltzer,Michael A. Boss,Robert H. Brown	2003	11
17	Rat LCR1: cloning and cellular distribution of a putative chemokine receptor in brain. PubMed ·Ma‐Li Wong,Winnie Xin,Ronald S. Duman	1996	35
18	Function of IHF in λ DNA Packaging Journal of Molecular Biology ·Winnie Xin,Maria Konyk,Michael Feiss	1993	24
19	Function of IHF in λ DNA Packaging Journal of Molecular Biology ·Winnie Xin,Michael Feiss	1993	36
20	Characterization and Functional Expression of a Somatostatin Receptor Coupled to Adenylyl Cyclase Molecular and Cellular Neuroscience ·Winnie Xin,Rosemarie Terwilliger,Joseph M. Rimland,Ma‐Li Wong,Eric J. Nestler,Ronald S. Duman	1993	2

About Winnie Xin

Winnie Xin is a scholar working on Physiology, Physiology, Genetics, Neurology and Cell Biology, having authored 29 papers that have together received 1.2k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (13 papers), Cellular transport and secretion (6 papers), Amyotrophic Lateral Sclerosis Research (5 papers), Neurogenetic and Muscular Disorders Research (4 papers), Calcium signaling and nucleotide metabolism (4 papers), Mitochondrial Function and Pathology (3 papers), Glycosylation and Glycoproteins Research (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Neurology (430 citations), Genetics (233 citations), Cell Biology (235 citations), Physiology (348 citations) and Neurology (107 citations). Winnie Xin has collaborated with scholars based in United States, Argentina and Sweden. Frequent co-authors include Katherine B. Sims, Michael Feiss, Hiroko Kishikawa, David M. Wu, Robert H. Brown, Yiping Shen, A. John Iafrate, Rebecca D. Folkerth, Wenhao Yu and John F. Staropoli. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Molecular Biology, PLoS ONE, Annals of Neurology and Gene.

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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