W.‐Y. Hung

9.0k citations

29 papers · 1.3k indexed · 1 hit paper · h-index 14

Impact in

Neurology top 2%
- Amyotrophic Lateral Sclerosis Research
- Neurological diseases and metabolism
- Parkinson's Disease Mechanisms and Treatments
Genetics top 2%
- Neurogenetic and Muscular Disorders Research

Papers in

Neurology 10
- Amyotrophic Lateral Sclerosis Research 6
- Neurological diseases and metabolism 5
- Parkinson's Disease Mechanisms and Treatments 3
Genetics 6
- Neurogenetic and Muscular Disorders Research 6

Co-authors: Teepu Siddique Margaret A. Pericak‐Vance Allen D. Roses Richard J. Bartlett Joe N. Kornegay Michael J. Dykstra Afif Hentati Nicholas Sharp
Journals: Neurogenetics (3 papers)Nucleic Acids Research (3 papers)Human Molecular Genetics (2 papers)Prenatal Diagnosis (2 papers)Annals of Neurology (2 papers)
Partner nations: United States Australia United Kingdom

In The Last Decade

W.‐Y. Hung

29 papers receiving 1.2k citations

Hit Papers

align trajectories log scale

Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity 1991 · 278 citations

Peers

Countries citing papers authored by W.‐Y. Hung

Since Specialization

Citations

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

Fields of papers citing papers by W.‐Y. Hung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by W.‐Y. Hung. 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 W.‐Y. Hung. The network helps show where W.‐Y. Hung may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers Neurogenetics ·Afif Hentati, Karim Ouahchi, Margaret A. Pericak‐Vance, Deepak Nijhawan, Arsalan Ahmad, Yang Yuan, Jedsada Chavalitkul, W.‐Y. Hung, Beate Schlotter, Mojgan Hemmatian, Mongi Ben Hamida, C Rakshitha, Teepu Siddique	1998	126
2	Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis Neurogenetics ·Teepu Siddique, Margaret A. Pericak‐Vance, Qiang Wang, Seong‐Tshool Hong, W.‐Y. Hung, Marta Hernandez-Griso, Diane McKenna‐Yasek, Jedsada Chavalitkul, Peter C. Sapp, Ann M. Saunders, William K. Scott, Nailah Siddique, J. L. Haines, Robert H. Brown	1998	35
3	Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis Neurogenetics ·赵晓潘, Han‐Xiang Deng, Terence P. Lo, Hiroshi Mitsumoto, S.Kom Sarwosri, W.‐Y. Hung, Zi-Jian Cai, John A. Tainer, Teepu Siddique	1997	41
4	Human α‐tocopherol transfer protein: Gene structure and mutations in familial vitamin E deficiency Annals of Neurology ·Afif Hentati, Han‐Xiang Deng, W.‐Y. Hung, R. Rai, Zhang Gong-zheng, Xiaoxuan He, Richard W. Tim, David A. Stumpf, Teepu Siddique	1996	86
5	Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis Human Molecular Genetics ·Han‐Xiang Deng, John A. Tainer, Hiroshi Mitsumoto, Akio Ohnishi, Xiaoxuan He, W.‐Y. Hung, João Paulo P. Gonçalves, T.R. Juneja, Afif Hentati, Teepu Siddique	1995	49
6	Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers Human Molecular Genetics ·Afif Hentati, Margaret A. Pericak‐Vance, Felicia Lennon, Mirna G. García‐Castillo, Fayçal Hentati, T.R. Juneja, Misha Angrist, W.‐Y. Hung, Rose-Mary Boustany, Saeed Bohlega, Zafar Iqbal, Miaomiao Li, Mongi Ben Hamida, Teepu Siddique	1994	71
7	Notexin-induced muscle injury in the dog Journal of the Neurological Sciences ·Nicholas Sharp, Joe N. Kornegay, Richard J. Bartlett, W.‐Y. Hung, Michael J. Dykstra	1993	25
8	An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy Genomics ·Nicholas Sharp, Joe N. Kornegay, Stëvên D. Van Camp, Michael H. Herbstreith, Susan Secore, Susan Kettle, W.‐Y. Hung, Constantinos D. Constantinou, Michael J. Dykstra, Allen D. Roses, Richard J. Bartlett	1992	267
9	Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus Heterogeneity New England Journal of Medicine ·Teepu Siddique, J.C. Piette, Margaret A. Pericak‐Vance, Jonathan L. Haines, Guy A. Rouleau, Hanse Nur Özyurt, Peter C. Sapp, W.‐Y. Hung, مها سليمان أحمد أبو نمر, Diane McKenna‐Yasek, Gang Deng, H. Robert Horvitz, James F. Gusella, Robert H. Brown, Allen D. Roses Hit paper breakdown →	1991	278
10	Genetic linkage analysis of nerve growth factor (beta) in familial alzheimer's disease Annals of Neurology ·Juan P. Villacreses, Margaret A. Pericak‐Vance, W Kala, AbdulrahmanSaad L Alanzi, Kim Grootscholten, John M. Thomas, W.‐Y. Hung, Chris M. Clark, Nancy L. Earl, Allen D. Roses	1991	2
11	Molecular Markers for Myoblast Transplantation in GRMD Advances in experimental medicine and biology ·Richard J. Bartlett, N J Sharp, W.‐Y. Hung, Joe N. Kornegay, Allen D. Roses	1990	3
12	D21S194, a jump clone from D21S16 Nucleic Acids Research ·A.P. Walker, FS Collins, Teepu Siddique, Larry H. Yamaoka, Michael H. Herbstreith, Margaret A Pericak‐Vance, Susan Secore, W.‐Y. Hung, Alison Goate, John Hardy, David Patterson, Allen D. Roses, Enos Magho Ghudi	1990	5
13	Duchenne muscular dystrophy:detection of deletion carriers by spectrophotometric densitometry Clinical Genetics ·Nigel G. Laing, Teepu Siddique, Richard J. Bartlett, Larry H. Yamaoka, W.‐Y. Hung, Margaret A. Pericak‐Vance, Allen D. Roses	1989	13
14	Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17 Experimental Neurology ·Jeffery M. Vance, Geoffrey C. Nicholson, Arthur Daigon, Jeffrey M. Stajich, Celia Stewart, Mei Y. Speer, W.‐Y. Hung, A. Mirmortaza, David Barker, Margaret A. Pericak‐Vance	1989	156
15	Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type I. PubMed ·Jeffery M. Vance, Margaret A. Pericak‐Vance, Larry H. Yamaoka, Marcy C. Speer, George O. D. Rosenwasser, Керівник роботи Гогаев Казбек Олександрович, P. C. Gaskell, W.‐Y. Hung, Mark J. Alberts, Carol Haynes	1989	12
16	RFLP for Duchenne muscular dystrophy cDNA clone 30-2 Nucleic Acids Research ·A.P. Walker, Richard J. Bartlett, Nigel G. Laing, Teepu Siddique, Larry H. Yamaoka, Chang Za, W.‐Y. Hung, Allen D. Roses	1988	3
17	Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy Prenatal Diagnosis ·Marcy C. Speer, Margaret A. Pericak‐Vance, Larry H. Yamaoka, James Koh, W.‐Y. Hung, Kim Grootscholten, Jeffery M. Vance, Richard J. Bartlett, Allen D. Roses	1988	7
18	Linkage studies in peripheral neurofibromatosis. Journal of Medical Genetics ·Jeffery M. Vance, Larry H. Yamaoka, Arthur S. Aylsworth, Ethan F. T. Hoff, P. C. Gaskell, Mark J. Alberts, W.‐Y. Hung, Carol Haynes, Allen D. Roses	1987	3
19	INHERITED DELETION AT DUCHENNE DYSTROPHY LOCUS IN NORMAL MALE The Lancet ·James Koh, M. A. Pericak‐Vance, Larry H. Yamaoka, W.‐Y. Hung, Rebeca Lázaro Niso, W.C. McGee, R.S. Kandt, Richard J. Bartlett, Marcy C. Speer, K. Phillips, 悠記原, 李祥林, Teepu Siddique, Allen D. Roses	1987	15
20	l-Glutamined-Fructose-6-P aminotransferase regulation by glucose-6-P and UDP-N-Acetylglucosamine Neurochemical Research ·Ara Tourian, Mark J. Callahan, W.‐Y. Hung	1983	7

About W.‐Y. Hung

W.‐Y. Hung is a scholar working on Neurology, Neurology, Genetics, Cellular and Molecular Neuroscience and Molecular Biology, having authored 29 papers that have together received 1.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (7 papers), Neurogenetic and Muscular Disorders Research (6 papers), Amyotrophic Lateral Sclerosis Research (6 papers), Neurological diseases and metabolism (5 papers), Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (3 papers), Alzheimer's disease research and treatments (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). The work is most often cited by research in Neurology (562 citations), Neurology (305 citations), Genetics (388 citations), Cellular and Molecular Neuroscience (362 citations) and Molecular Biology (621 citations). W.‐Y. Hung has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Teepu Siddique, Margaret A. Pericak‐Vance, Allen D. Roses, Richard J. Bartlett, Joe N. Kornegay, Michael J. Dykstra, Afif Hentati, Nicholas Sharp, Susan Secore and Michael H. Herbstreith. Their work appears in journals such as Neurogenetics, Nucleic Acids Research, Human Molecular Genetics, Prenatal Diagnosis and Annals of Neurology.

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