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Jeffrey S Hall

Jeffrey Hall is a Research Virologist at the National Wildlife Health Center.

Professional Experience

  • Sept. 2007 - Present Research Virologist USGS National Wildlife Health Center, Madison, WI

  • Sept. 2003 - Sept. 2007 Virologist/ Laboratory Manager USDA-APHIS-NWRC. Ft. Collins, CO

  • July 1997 - Sept. 2003 Microbiologist USDA-ARS. Lincoln, NE

  • March 1991 - July 1997 Research Associate Department of Plant Pathology. University of Nebraska-Lincoln, Lincoln, NE

Education and Certifications

  • 2001 Doctor of Philosophy, Comparative Pathobiology, University of Nebraska-Lincoln, Lincoln, NE

Science and Products

link
Image: Northern Pintail Ducks

Avian Influenza

Avian influenza is a viral disease caused by various strains of avian influenza viruses that can be classified as low pathogenic avian influenza (LPAI) or highly pathogenic avian influenza (HPAI). It remains a global disease with potential high consequence with the potential to threaten wildlife, agriculture, and human health.
By
Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center
link

Avian Influenza

Avian influenza is a viral disease caused by various strains of avian influenza viruses that can be classified as low pathogenic avian influenza (LPAI) or highly pathogenic avian influenza (HPAI). It remains a global disease with potential high consequence with the potential to threaten wildlife, agriculture, and human health.
Learn More
link
Mosquito, species not verified

Vector-Borne Diseases

Vector-borne diseases are transmitted from one animal to another by vectors, including insects, such as mosquitoes or fleas, and arachnids, such as ticks. The USGS National Wildlife Health Center investigates wildlife diseases, including vector-borne diseases, such as West Nile virus and sylvatic plague.
By
Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center
link

Vector-Borne Diseases

Vector-borne diseases are transmitted from one animal to another by vectors, including insects, such as mosquitoes or fleas, and arachnids, such as ticks. The USGS National Wildlife Health Center investigates wildlife diseases, including vector-borne diseases, such as West Nile virus and sylvatic plague.
Learn More

Dataset: Acute oral toxicity and tissue residues of saxitoxin in the mallard (Anas platyrhynchos)

This data set is composed of data collected from an experimental study inoculating mallard ducks (Anas platyrhynchos) with Saxitoxin and associated control ducks. Data includes the specific of inoculation, observational behavioral data, daily weights, dosing, results of inoculation, testing of samples collected throughout the study, and necropsy results.
By
National Wildlife Health Center
Filter Total Items: 44

Acute oral toxicity and tissue residues of saxitoxin in the mallard (Anas platyrhynchos)

Since 2014, widespread, annual mortality events involving multiple species of seabirds have occurred in the Gulf of Alaska, Bering Sea, and Chukchi Sea. Among these die-offs, emaciation was a common finding with starvation often identified as the cause of death. However, saxitoxin (STX) was detected in many carcasses, indicating exposure of these seabirds to STX in the marine environment. Few data
By
Ecosystems, National Wildlife Health Center

Highly pathogenic avian influenza virus H5N2 (Clade 2.3.4.4) challenge of mallards age appropriate to the 2015 midwestern poultry outbreak

BackgroundThe 2015 highly pathogenic avian influenza virus (HPAIV) H5N2 clade 2.3.4.4 outbreak in upper midwestern U.S. poultry operations was not detected in wild birds to any great degree during the outbreak, despite wild waterfowl being implicated in the introduction, reassortment, and movement of the virus into North America from Asia. This outbreak led to the demise of over 50 million domesti
By
Ecosystems, National Wildlife Health Center

Experimental challenge of a North American bat species, big brown bat (Eptesicus fuscus), with SARS-CoV-2

The recently emerged novel coronavirus, SARS‐CoV‐2, is phylogenetically related to bat coronaviruses (CoVs), specifically SARS‐related CoVs from the Eurasian bat family Rhinolophidae. As this human pandemic virus has spread across the world, the potential impacts of SARS‐CoV‐2 on native North American bat populations are unknown, as is the ability of North American bats to serve as reservoirs or i
By
Ecosystems, National Wildlife Health Center

Serosurvey of coyotes (Canis latrans), foxes (Vulpes vulpes, Urocyon cinereoargenteus) and raccoons (Procyon lotor) for exposure to influenza A viruses in the USA

We tested coyote (Canis latrans), fox (Urocyon cinereoargenteus, Vulpes vulpes), and raccoon (Procyon lotor) sera for influenza A virus (IAV) exposure. We found 2/139 samples (1 coyote, 1 raccoon) had IAV antibodies and hemagglutination inhibition assays revealed the antibodies to the 2009/2010 H1N1 human pandemic virus or to the 2007 human seasonal H1N1 virus.
By
Ecosystems, National Wildlife Health Center

Inactivation of viable surrogates for the select agents virulent Newcastle disease virus and highly pathogenic avian influenza virus using either commercial lysis buffer or heat

Introduction:Federal Select Agent Program regulations require laboratories to document a validated procedure for inactivating select agents prior to movement outside registered space. Avian influenza viruses and virulent Newcastle disease virus (vNDV) are cultured in chicken amnio-allantoic fluid (AAF), but the efficacy of commercial lysis buffers to inactivate viruses in protein-rich media has no
By
Ecosystems, National Wildlife Health Center

Avian influenza virus prevalence in marine birds is dependent on ocean temperatures

Waterfowl and shorebirds are the primary hosts of influenza A virus (IAV), however, in most surveillance efforts, large populations of birds are not routinely examined; specifically marine ducks and other birds that reside predominately on or near the ocean. We conducted a long-term study sampling sea ducks and gulls in coastal Maine for IAV and found a virus prevalence (1.7%) much lower than is t
By
Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

Aerosol transmission of gull-origin Iceland subtype H10N7 influenza A virus in ferrets

Subtype H10 influenza A viruses (IAVs) have been recovered from domestic poultry and various aquatic bird species, and sporadic transmission of these IAVs from avian species to mammals (i.e., human, seal, and mink) are well documented. In 2015, we isolated four H10N7 viruses from gulls in Iceland. Genomic analyses showed four gene segments in the viruses were genetically associated with H10 IAVs t
By
Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

Influenza A virus recovery, diversity, and intercontinental exchange: A multi-year assessment of wild bird sampling at Izembek National Wildlife Refuge, Alaska

Western Alaska is a potential point-of-entry for foreign-origin influenza A viruses (IAVs) into North America via migratory birds. We sampled waterfowl and gulls for IAVs at Izembek National Wildlife Refuge (NWR) in western Alaska, USA, during late summer and autumn months of 2011–2015, to evaluate the abundance and diversity of viruses at this site. We collected 4842 samples across five years fro
By
Ecosystems, Fish & Wildlife Disease, Alaska Science Center, National Wildlife Health Center

Infectious canine hepatitis in a brown bear (Ursus arctos horribilis) from Alaska.

We diagnosed infectious canine hepatitis in a free-ranging brown bear (Ursus arctos horribilis) cub from Alaska, US, found dead in October 2015. Intranuclear inclusion bodies were present in hepatocytes, and immunohistochemistry showed reactivity to adenoviral antigens. Sequencing of the hexon protein of adenovirus showed 100% identity to canine adenovirus 1.
By
Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

Inferring epidemiologic dynamics from viral evolution: 2014–2015 Eurasian/North American highly pathogenic avian influenza viruses exceed transmission threshold, R0 = 1, in wild birds and poultry in North America

Highly pathogenic avian influenza virus (HPAIV) is a multihost pathogen with lineages that pose health risks for domestic birds, wild birds, and humans. One mechanism of intercontinental HPAIV spread is through wild bird reservoirs, and wild birds were the likely sources of a Eurasian (EA) lineage HPAIV into North America in 2014. The introduction resulted in several reassortment events with North
By
Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

Experimental infection of common eider ducklings with Wellfleet Bay virus, a newly characterized orthomyxovirus

Wellfleet Bay virus (WFBV), a novel orthomyxovirus in the genus Quaranjavirus, was first isolated in 2006 from carcasses of common eider (Somateria mollissima) during a mortality event in Wellfleet Bay (Barnstable County, Massachusetts, USA) and has since been repeatedly isolated during recurrent mortality events in this location. Hepatic, pancreatic, splenic, and intestinal necrosis were observed
By
Ecosystems, National Wildlife Health Center

Lambdapapillomavirus 2 in a gray wolf (Canis lupus) from Minnesota with oral papillomatosis and sarcoptic mange

Oral papillomatosis was diagnosed in a gray wolf (Canis lupus) with sarcoptic mange from Minnesota, USA found dead in February 2015. Intranuclear inclusion bodies were evident histologically, and papillomaviral antigens were confirmed using immunohistochemistry. Sequencing of the L1 papillomavirus gene showed closest similarity to Lambdapapillomavirus 2.
By
Ecosystems, National Wildlife Health Center

Pre-USGS Publications

Kaci K. VanDalen, Jeffrey S. Hall, Larry Clark, Robert G. McLean, Cynthia Smeraski. (2013) West Nile virus infection in American robins: New insights on dose response. PLoS One. 10.1371/journal.pone.0068537.
Paul Oesterle, Nicole Nemeth, Ginger Young, Nicole Mooers, Stacey Elmore, Richard Bowen, Paul Doherty, Jeffrey Hall, Robert McLean and Larry Clark. (2010) Cliff swallows, swallow bugs, and West Nile virus: an unlikely transmission mechanism. Vec. Borne Zoon. Dis. 10(5): 507-513.
Oesterle P, Nemeth N, VanDalen K, Sullivan H, Bentler K, Young G, McLean R, Clark L, Smeraski C and Hall JS. (2009) Experimental infection of cliff swallows (Petrochelidon pyrrhonota) with varying doses of West Nile virus. Am. J. Trop. Med. Hyg. 81:1159-1164.
10.4269/ajtmh.2009.09-0136
Jeffrey S. Hall, Kevin Bentler, Gabrielle Landolt, Richard B. Minnis, Tyler A. Campbell, Scott C. Barras, J. Jeffrey Root, Stacy Elmore, John Pilon, Kristy Pabilonia, Cindy Driscoll, Dennis Slate, Heather Sullivan and Robert G. McLean. (2008) Influenza infection in wild raccoons. Emerg. Inf. Dis. 14:1842-1848.
https://doi.org/10.3201/eid1412.071371
Jeffrey S. Hall, Rich Minnis, Tyler A. Campbell, Scott Barras, Randy W. DeYoung, Kristy Pabilonia, Michael Avery, Heather Sullivan, Larry Clark and Robert G. McLean. (2008) Influenza exposure in United States feral swine populations. J. Wildlife Dis. 44:362-368.
https://doi.org/10.7589/0090-3558-44.2.362
Britch, SC, Linthicum KJ, and Rift Valley Fever Working Group. (2007) Developing a research agenda and a comprehensive national prevention and response plan for Rift Valley fever in the United States. Emerg. Inf. Dis. [serial on the Internet] Available from http://www.cdc.gov/EID/content/13/8/e1.htm.
McLean, R.G., J.S. Hall, A.B. Franklin, H. Sullivan, K. VanDalen, S. Shriner, M. Farnsworth, P. Oesterle, G. Young, J. Carlson, K. Cobble, T. Deliberto, S. Swafford, S. Elmore, T. Anderson, S. Hauser, K. Bentler, N. Mooers and K. Huyvaert . (2007) Avian influenza in wild birds: environmental sampling strategy for the rapid detection of avian influenza viruses. Proceedings of the 12th Wildlife Damage Management Conference, Corpus Christi, TX.
Root, J., P. Oesterle, H. Sullivan, J.S. Hall, N. Marlenee, R.G. McLean, J.A. Montenieri and L. Clark. Fox squirrel (Sciuris niger) associations with West Nile virus. (2007) Am. J. Trop. Med. Hyg. 76:782-784.
Bentler, K., J.S. Hall, J. Root, K. Klenk, B. Schmitt and L. Clark. (2007) West Nile Virus seroprevalence in North American mesopredators. Am. J. Trop. Med. Hyg. 76:173-179.
Root, J.Jeffrey, P. Oesterle, N. Nemeth, K. Klenk, D.H. Gould, R.G. McLean, L. Clark and J.S. Hall. (2006) Experimental infection of fox squirrels (Sciurus niger) with West Nile virus. Am. J. Trop. Med. Hyg. 75:697-701.
Clark, L., J.S. Hall, R. McLean, M. Dunbar, K. Klenk, Richard Bowen and C.A. Smeraski. (2006) Susceptibility of greater sage-grouse to experimental infection with West Nile virus. J. Wildlife Dis. 42:14-22.
L. Clark and J. S. Hall. (2006) Avian influenza in wild birds: status as reservoirs and risks posed to humans and agriculture. Ornithological Monographs 60:3-29.
Santaella-Tenorio, J., R. McLean, J.S. Gill, R. Bowen, J. S. Hall and L. Clark. (2005) West Nile virus serosurveillance in Iowa white-tailed deer (1999-2003). Am. J. Trop. Med. Hyg. 73: 1038-1042).
Root, J.J., Hall J.S., McLean, R.G., Marlenee, N.L., Beaty, B.J., Gansowski, J. and Clark, L. (2005) Serologic evidence of exposure of wild mammals to Flaviviruses in the central and eastern United States. Am. J. Trop. Med. Hyg. 72: 622-630.
Hall J.S., French R., Morris T.J. and Stenger D.C. (2001) Structure and temporal dynamics of populations within wheat streak mosaic virus isolates. J. Virol. 75: 10231-10243.
Hall J.S., French R., Hein G.L., Morris T.J. and Stenger D.C. (2001) Three distinct mechanisms facilitate genetic isolation of sympatric wheat streak mosaic virus lineages. Virology 282: 230-236.
Choi I.-R., Hall J.S., Henry M., Zhang L., Hein G.L., French R. and Stenger D.C. (2000) Contributions of genetic drift and negative selection on the evolution of three strains of wheat streak mosaic tritimovirus. Arch. Virol. 146: 619-628.
Hall J.S., Adams B., Parsons T.J., French R., Lane L.C. and Jensen S.G. (1998) Molecular cloning, sequencing, and phylogenetic relationships of a new Potyvirus: sugarcane streak mosaic virus, and a reevaluation of the classification of the Potyviridae. Mol. Phylo. Evol. 10: 323-332.
Stenger D.C., Hall J.S., Choi I.-R. and French R. (1998) Phylogenetic relationships within the family Potyviridae: Wheat streak mosaic virus and brome streak mosaic virus are not members of the genus Rymovirus. Phytopathology 88: 782-787.
Marcon, A., Kaeppler, S.M. Jensen, S.G. and Hall, J.S. 1996. Characteristics of the High Plains Virus (HPV) and breeding for resistance in maize. Proceedings of the Latin American Workshop on Maize Diseases. Sete Lagoas, MG, Brazil May 20-24, 1996. Publisher EMBRAPA, E. de Oliveira Editor.
S.G. Jensen and J.S. Hall. (1993) Characterization of a Krish-sorghum infecting potyvirus. Sorghum Newsletter 34:17
F.L. Smith, S.W. Carper, J.S. Hall, B.J. Gilligan, E.L. Madsen and F.K. Storm. (1992) Cellular effects of piezoelectric versus electrohydraulic high energy shock waves. J. Urology 147:491-495.
S.W. Carper, J.S. Hall and F.K. Storm. (1992) Thermal protection by prostaglandin E1, a preclinical study. Reg. Cancer Treatment 4:156-158.

Science and Products

  • Science
    link
    Image: Northern Pintail Ducks

    Avian Influenza

    Avian influenza is a viral disease caused by various strains of avian influenza viruses that can be classified as low pathogenic avian influenza (LPAI) or highly pathogenic avian influenza (HPAI). It remains a global disease with potential high consequence with the potential to threaten wildlife, agriculture, and human health.
    By
    Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center
    link

    Avian Influenza

    Avian influenza is a viral disease caused by various strains of avian influenza viruses that can be classified as low pathogenic avian influenza (LPAI) or highly pathogenic avian influenza (HPAI). It remains a global disease with potential high consequence with the potential to threaten wildlife, agriculture, and human health.
    Learn More
    link
    Mosquito, species not verified

    Vector-Borne Diseases

    Vector-borne diseases are transmitted from one animal to another by vectors, including insects, such as mosquitoes or fleas, and arachnids, such as ticks. The USGS National Wildlife Health Center investigates wildlife diseases, including vector-borne diseases, such as West Nile virus and sylvatic plague.
    By
    Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center
    link

    Vector-Borne Diseases

    Vector-borne diseases are transmitted from one animal to another by vectors, including insects, such as mosquitoes or fleas, and arachnids, such as ticks. The USGS National Wildlife Health Center investigates wildlife diseases, including vector-borne diseases, such as West Nile virus and sylvatic plague.
    Learn More
  • Data

    Dataset: Acute oral toxicity and tissue residues of saxitoxin in the mallard (Anas platyrhynchos)

    This data set is composed of data collected from an experimental study inoculating mallard ducks (Anas platyrhynchos) with Saxitoxin and associated control ducks. Data includes the specific of inoculation, observational behavioral data, daily weights, dosing, results of inoculation, testing of samples collected throughout the study, and necropsy results.
    By
    National Wildlife Health Center
  • Publications
    Filter Total Items: 44

    Acute oral toxicity and tissue residues of saxitoxin in the mallard (Anas platyrhynchos)

    Since 2014, widespread, annual mortality events involving multiple species of seabirds have occurred in the Gulf of Alaska, Bering Sea, and Chukchi Sea. Among these die-offs, emaciation was a common finding with starvation often identified as the cause of death. However, saxitoxin (STX) was detected in many carcasses, indicating exposure of these seabirds to STX in the marine environment. Few data
    By
    Ecosystems, National Wildlife Health Center

    Highly pathogenic avian influenza virus H5N2 (Clade 2.3.4.4) challenge of mallards age appropriate to the 2015 midwestern poultry outbreak

    BackgroundThe 2015 highly pathogenic avian influenza virus (HPAIV) H5N2 clade 2.3.4.4 outbreak in upper midwestern U.S. poultry operations was not detected in wild birds to any great degree during the outbreak, despite wild waterfowl being implicated in the introduction, reassortment, and movement of the virus into North America from Asia. This outbreak led to the demise of over 50 million domesti
    By
    Ecosystems, National Wildlife Health Center

    Experimental challenge of a North American bat species, big brown bat (Eptesicus fuscus), with SARS-CoV-2

    The recently emerged novel coronavirus, SARS‐CoV‐2, is phylogenetically related to bat coronaviruses (CoVs), specifically SARS‐related CoVs from the Eurasian bat family Rhinolophidae. As this human pandemic virus has spread across the world, the potential impacts of SARS‐CoV‐2 on native North American bat populations are unknown, as is the ability of North American bats to serve as reservoirs or i
    By
    Ecosystems, National Wildlife Health Center

    Serosurvey of coyotes (Canis latrans), foxes (Vulpes vulpes, Urocyon cinereoargenteus) and raccoons (Procyon lotor) for exposure to influenza A viruses in the USA

    We tested coyote (Canis latrans), fox (Urocyon cinereoargenteus, Vulpes vulpes), and raccoon (Procyon lotor) sera for influenza A virus (IAV) exposure. We found 2/139 samples (1 coyote, 1 raccoon) had IAV antibodies and hemagglutination inhibition assays revealed the antibodies to the 2009/2010 H1N1 human pandemic virus or to the 2007 human seasonal H1N1 virus.
    By
    Ecosystems, National Wildlife Health Center

    Inactivation of viable surrogates for the select agents virulent Newcastle disease virus and highly pathogenic avian influenza virus using either commercial lysis buffer or heat

    Introduction:Federal Select Agent Program regulations require laboratories to document a validated procedure for inactivating select agents prior to movement outside registered space. Avian influenza viruses and virulent Newcastle disease virus (vNDV) are cultured in chicken amnio-allantoic fluid (AAF), but the efficacy of commercial lysis buffers to inactivate viruses in protein-rich media has no
    By
    Ecosystems, National Wildlife Health Center

    Avian influenza virus prevalence in marine birds is dependent on ocean temperatures

    Waterfowl and shorebirds are the primary hosts of influenza A virus (IAV), however, in most surveillance efforts, large populations of birds are not routinely examined; specifically marine ducks and other birds that reside predominately on or near the ocean. We conducted a long-term study sampling sea ducks and gulls in coastal Maine for IAV and found a virus prevalence (1.7%) much lower than is t
    By
    Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

    Aerosol transmission of gull-origin Iceland subtype H10N7 influenza A virus in ferrets

    Subtype H10 influenza A viruses (IAVs) have been recovered from domestic poultry and various aquatic bird species, and sporadic transmission of these IAVs from avian species to mammals (i.e., human, seal, and mink) are well documented. In 2015, we isolated four H10N7 viruses from gulls in Iceland. Genomic analyses showed four gene segments in the viruses were genetically associated with H10 IAVs t
    By
    Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

    Influenza A virus recovery, diversity, and intercontinental exchange: A multi-year assessment of wild bird sampling at Izembek National Wildlife Refuge, Alaska

    Western Alaska is a potential point-of-entry for foreign-origin influenza A viruses (IAVs) into North America via migratory birds. We sampled waterfowl and gulls for IAVs at Izembek National Wildlife Refuge (NWR) in western Alaska, USA, during late summer and autumn months of 2011–2015, to evaluate the abundance and diversity of viruses at this site. We collected 4842 samples across five years fro
    By
    Ecosystems, Fish & Wildlife Disease, Alaska Science Center, National Wildlife Health Center

    Infectious canine hepatitis in a brown bear (Ursus arctos horribilis) from Alaska.

    We diagnosed infectious canine hepatitis in a free-ranging brown bear (Ursus arctos horribilis) cub from Alaska, US, found dead in October 2015. Intranuclear inclusion bodies were present in hepatocytes, and immunohistochemistry showed reactivity to adenoviral antigens. Sequencing of the hexon protein of adenovirus showed 100% identity to canine adenovirus 1.
    By
    Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

    Inferring epidemiologic dynamics from viral evolution: 2014–2015 Eurasian/North American highly pathogenic avian influenza viruses exceed transmission threshold, R0 = 1, in wild birds and poultry in North America

    Highly pathogenic avian influenza virus (HPAIV) is a multihost pathogen with lineages that pose health risks for domestic birds, wild birds, and humans. One mechanism of intercontinental HPAIV spread is through wild bird reservoirs, and wild birds were the likely sources of a Eurasian (EA) lineage HPAIV into North America in 2014. The introduction resulted in several reassortment events with North
    By
    Ecosystems, Fish & Wildlife Disease, National Wildlife Health Center

    Experimental infection of common eider ducklings with Wellfleet Bay virus, a newly characterized orthomyxovirus

    Wellfleet Bay virus (WFBV), a novel orthomyxovirus in the genus Quaranjavirus, was first isolated in 2006 from carcasses of common eider (Somateria mollissima) during a mortality event in Wellfleet Bay (Barnstable County, Massachusetts, USA) and has since been repeatedly isolated during recurrent mortality events in this location. Hepatic, pancreatic, splenic, and intestinal necrosis were observed
    By
    Ecosystems, National Wildlife Health Center

    Lambdapapillomavirus 2 in a gray wolf (Canis lupus) from Minnesota with oral papillomatosis and sarcoptic mange

    Oral papillomatosis was diagnosed in a gray wolf (Canis lupus) with sarcoptic mange from Minnesota, USA found dead in February 2015. Intranuclear inclusion bodies were evident histologically, and papillomaviral antigens were confirmed using immunohistochemistry. Sequencing of the L1 papillomavirus gene showed closest similarity to Lambdapapillomavirus 2.
    By
    Ecosystems, National Wildlife Health Center

    Pre-USGS Publications

    Kaci K. VanDalen, Jeffrey S. Hall, Larry Clark, Robert G. McLean, Cynthia Smeraski. (2013) West Nile virus infection in American robins: New insights on dose response. PLoS One. 10.1371/journal.pone.0068537.
    Paul Oesterle, Nicole Nemeth, Ginger Young, Nicole Mooers, Stacey Elmore, Richard Bowen, Paul Doherty, Jeffrey Hall, Robert McLean and Larry Clark. (2010) Cliff swallows, swallow bugs, and West Nile virus: an unlikely transmission mechanism. Vec. Borne Zoon. Dis. 10(5): 507-513.
    Oesterle P, Nemeth N, VanDalen K, Sullivan H, Bentler K, Young G, McLean R, Clark L, Smeraski C and Hall JS. (2009) Experimental infection of cliff swallows (Petrochelidon pyrrhonota) with varying doses of West Nile virus. Am. J. Trop. Med. Hyg. 81:1159-1164.
    10.4269/ajtmh.2009.09-0136
    Jeffrey S. Hall, Kevin Bentler, Gabrielle Landolt, Richard B. Minnis, Tyler A. Campbell, Scott C. Barras, J. Jeffrey Root, Stacy Elmore, John Pilon, Kristy Pabilonia, Cindy Driscoll, Dennis Slate, Heather Sullivan and Robert G. McLean. (2008) Influenza infection in wild raccoons. Emerg. Inf. Dis. 14:1842-1848.
    https://doi.org/10.3201/eid1412.071371
    Jeffrey S. Hall, Rich Minnis, Tyler A. Campbell, Scott Barras, Randy W. DeYoung, Kristy Pabilonia, Michael Avery, Heather Sullivan, Larry Clark and Robert G. McLean. (2008) Influenza exposure in United States feral swine populations. J. Wildlife Dis. 44:362-368.
    https://doi.org/10.7589/0090-3558-44.2.362
    Britch, SC, Linthicum KJ, and Rift Valley Fever Working Group. (2007) Developing a research agenda and a comprehensive national prevention and response plan for Rift Valley fever in the United States. Emerg. Inf. Dis. [serial on the Internet] Available from http://www.cdc.gov/EID/content/13/8/e1.htm.
    McLean, R.G., J.S. Hall, A.B. Franklin, H. Sullivan, K. VanDalen, S. Shriner, M. Farnsworth, P. Oesterle, G. Young, J. Carlson, K. Cobble, T. Deliberto, S. Swafford, S. Elmore, T. Anderson, S. Hauser, K. Bentler, N. Mooers and K. Huyvaert . (2007) Avian influenza in wild birds: environmental sampling strategy for the rapid detection of avian influenza viruses. Proceedings of the 12th Wildlife Damage Management Conference, Corpus Christi, TX.
    Root, J., P. Oesterle, H. Sullivan, J.S. Hall, N. Marlenee, R.G. McLean, J.A. Montenieri and L. Clark. Fox squirrel (Sciuris niger) associations with West Nile virus. (2007) Am. J. Trop. Med. Hyg. 76:782-784.
    Bentler, K., J.S. Hall, J. Root, K. Klenk, B. Schmitt and L. Clark. (2007) West Nile Virus seroprevalence in North American mesopredators. Am. J. Trop. Med. Hyg. 76:173-179.
    Root, J.Jeffrey, P. Oesterle, N. Nemeth, K. Klenk, D.H. Gould, R.G. McLean, L. Clark and J.S. Hall. (2006) Experimental infection of fox squirrels (Sciurus niger) with West Nile virus. Am. J. Trop. Med. Hyg. 75:697-701.
    Clark, L., J.S. Hall, R. McLean, M. Dunbar, K. Klenk, Richard Bowen and C.A. Smeraski. (2006) Susceptibility of greater sage-grouse to experimental infection with West Nile virus. J. Wildlife Dis. 42:14-22.
    L. Clark and J. S. Hall. (2006) Avian influenza in wild birds: status as reservoirs and risks posed to humans and agriculture. Ornithological Monographs 60:3-29.
    Santaella-Tenorio, J., R. McLean, J.S. Gill, R. Bowen, J. S. Hall and L. Clark. (2005) West Nile virus serosurveillance in Iowa white-tailed deer (1999-2003). Am. J. Trop. Med. Hyg. 73: 1038-1042).
    Root, J.J., Hall J.S., McLean, R.G., Marlenee, N.L., Beaty, B.J., Gansowski, J. and Clark, L. (2005) Serologic evidence of exposure of wild mammals to Flaviviruses in the central and eastern United States. Am. J. Trop. Med. Hyg. 72: 622-630.
    Hall J.S., French R., Morris T.J. and Stenger D.C. (2001) Structure and temporal dynamics of populations within wheat streak mosaic virus isolates. J. Virol. 75: 10231-10243.
    Hall J.S., French R., Hein G.L., Morris T.J. and Stenger D.C. (2001) Three distinct mechanisms facilitate genetic isolation of sympatric wheat streak mosaic virus lineages. Virology 282: 230-236.
    Choi I.-R., Hall J.S., Henry M., Zhang L., Hein G.L., French R. and Stenger D.C. (2000) Contributions of genetic drift and negative selection on the evolution of three strains of wheat streak mosaic tritimovirus. Arch. Virol. 146: 619-628.
    Hall J.S., Adams B., Parsons T.J., French R., Lane L.C. and Jensen S.G. (1998) Molecular cloning, sequencing, and phylogenetic relationships of a new Potyvirus: sugarcane streak mosaic virus, and a reevaluation of the classification of the Potyviridae. Mol. Phylo. Evol. 10: 323-332.
    Stenger D.C., Hall J.S., Choi I.-R. and French R. (1998) Phylogenetic relationships within the family Potyviridae: Wheat streak mosaic virus and brome streak mosaic virus are not members of the genus Rymovirus. Phytopathology 88: 782-787.
    Marcon, A., Kaeppler, S.M. Jensen, S.G. and Hall, J.S. 1996. Characteristics of the High Plains Virus (HPV) and breeding for resistance in maize. Proceedings of the Latin American Workshop on Maize Diseases. Sete Lagoas, MG, Brazil May 20-24, 1996. Publisher EMBRAPA, E. de Oliveira Editor.
    S.G. Jensen and J.S. Hall. (1993) Characterization of a Krish-sorghum infecting potyvirus. Sorghum Newsletter 34:17
    F.L. Smith, S.W. Carper, J.S. Hall, B.J. Gilligan, E.L. Madsen and F.K. Storm. (1992) Cellular effects of piezoelectric versus electrohydraulic high energy shock waves. J. Urology 147:491-495.
    S.W. Carper, J.S. Hall and F.K. Storm. (1992) Thermal protection by prostaglandin E1, a preclinical study. Reg. Cancer Treatment 4:156-158.