Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder von Katsanis, Nicholas, Ansley, Stephen J., Badano, Jose L., Eichers, Erica R., Lewis, Richard Alan, Hoskins, Bethan E., Scambler, Peter J., Davidson, William S., Beales, Philip L., Lupski, James R.

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Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome von Katsanis, Nicholas, Ansley, Stephen J, Badano, Jose L, Blacque, Oliver E, Hill, Josephine, Hoskins, Bethan E, Leitch, Carmen C, Chul Kim, Jun, Ross, Alison J, Eichers, Erica R, Teslovich, Tanya M, Mah, Allan K, Johnsen, Robert C, Cavender, John C, Alan Lewis, Richard, Leroux, Michel R, Beales, Philip L

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Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport von Blacque, Oliver E, Reardon, Michael J, Li, Chunmei, McCarthy, Jonathan, Mahjoub, Moe R, Ansley, Stephen J, Badano, Jose L, Mah, Allan K, Beales, Philip L, Davidson, William S, Johnsen, Robert C, Audeh, Mark, Plasterk, Ronald H A, Baillie, David L, Katsanis, Nicholas, Quarmby, Lynne M, Wicks, Stephen R, Leroux, Michel R

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Identification of a Novel Bardet-Biedl Syndrome Protein, BBS7, That Shares Structural Features with BBS1 and BBS2 von Badano, José L., Ansley, Stephen J., Leitch, Carmen C., Lewis, Richard Alan, Lupski, James R., Katsanis, Nicholas

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Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet–Biedl patients with two mutations at a second BBS locus von Badano, Jose L., Kim, Jun Chul, Hoskins, Bethan E., Lewis, Richard Alan, Ansley, Stephen J., Cutler, David J., Castellan, Claudio, Beales, Philip L., Leroux, Michel R., Katsanis, Nicholas

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Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome von Lupski, James R, Katsanis, Nicholas, Beales, Philip L, Woods, Michael O, Lewis, Richard A, Green, Jane S, Parfrey, Patrick S, Ansley, Stephen J, Davidson, William S

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Short- and long-term outcomes for patients with variceal haemorrhage in a tertiary hospital von Halland, M., Ansley, S. J., Stokes, B. J., Fitzgerald, M. N., Inder, K. J., Duggan, J. M., Duggan, A.

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BBS4 Is a Minor Contributor to Bardet-Biedl Syndrome and May Also Participate in Triallelic Inheritance von Katsanis, Nicholas, Eichers, Erica R., Ansley, Stephen J., Lewis, Richard Alan, Kayserili, Hülya, Hoskins, Bethan E., Scambler, Peter J., Beales, Philip L., Lupski, James R.

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Genetic and Mutational Analyses of a Large Multiethnic Bardet-Biedl Cohort Reveal a Minor Involvement of BBS6 and Delineate the Critical Intervals of Other Loci von Beales, Philip L., Katsanis, Nicholas, Lewis, Richard A., Ansley, Stephen J., Elcioglu, Nursel, Raza, Jamal, Woods, Michael O., Green, Jane S., Parfrey, Patrick S., Davidson, William S., Lupski, James R.

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A Computational/Functional Genomics Approach for the Enrichment of the Retinal Transcriptome and the Identification of Positional Candidate Retinopathy Genes von Katsanis, Nicholas, Worley, Kim C., Gonzalez, Guillermo, Ansley, Stephen J., Lupski, James R.

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Dissection of epistasis in oligogenic Bardet-Biedl syndrome von Fisher, Shannon, Ansley, Stephen J, Lewis, Richard Alan, Katsanis, Nicholas, Beales, Philip L, Lawson, Shaneka, Leitch, Carmen C, Badano, Jose L, Dietz, Harry C, May-Simera, Helen

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The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression von Leroux, Michel R, Katsanis, Nicholas, Kim, Jun Chul, Badano, Jose L, Sibold, Sonja, Esmail, Muneer A, Hill, Josephine, Hoskins, Bethan E, Leitch, Carmen C, Venner, Kerrie, Ansley, Stephen J, Ross, Alison J, Beales, Philip L

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Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome von Davidson, William S, Leroux, Michel R, Fan, Yanli, Esmail, Muneer A, Ansley, Stephen J, Blacque, Oliver E, Boroevich, Keith, Ross, Alison J, Moore, Susan J, Badano, Jose L, May-Simera, Helen, Compton, Deanna S, Green, Jane S, Lewis, Richard Alan, van Haelst, Mieke M, Parfrey, Patrick S, Baillie, David L, Beales, Philip L, Katsanis, Nicholas

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Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome von Beales, Philip L., Badano, Jose L., Ross, Alison J., Ansley, Stephen J., Hoskins, Bethan E., Kirsten, Brigitta, Mein, Charles A., Froguel, Philippe, Scambler, Peter J., Lewis, Richard Alan, Lupski, James R., Katsanis, Nicholas

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Forest composition, structure, and change in an old-growth mixed conifer forest in the northern Sierra Nevada von Ansley, J.A.S. (University of California-Berkeley, Berkeley, CA.), Battles, J.J

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Sound Scattering by a Layered Sphere von Ansley,S J, Skelton,E A

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CRYOGENICS AS APPLIED TO THE DESIGN AND FABRICATION OF A SPACE SIMULATION TEST CELL von ANSLEY,S P ,JR

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Pathophysiological mechanisms of exercise‐induced anaphylaxis: an EAACI position statement von Ansley, L., Bonini, M., Delgado, L., Del Giacco, S., Du Toit, G., Khaitov, M., Kurowski, M., Hull, J. H., Moreira, A., Robson‐Ansley, P. J.

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Athletic trainers’ viewpoints of patient-centered care: Preliminary findings von Wilson, Carly J, Eberman, Lindsey E, Redinger, Ansley S, Neil, Elizabeth R, Winkelmann, Zachary K

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Relative predictive value of sociodemographic factors for chronic diseases among All of Us participants: a descriptive analysis von Kunnath, Ansley J, Sack, Daniel E, Wilkins, Consuelo H

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