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Facilitating health data sharing across diverse practices and communities.

Summit on translational bioinformatics

Lin CP, Black RA, Laplante J, Keppel GA, Tuzzio L, Berg AO, Whitener RJ, Buchwald DS, Baldwin LM, Fishman PA, Greene SM, Gennari JH, Tarczy-Hornoch P, Stephens KA.
PMID: 21347138
Summit Transl Bioinform. 2010 Mar 01;2010:16-20.

Health data sharing with and among practices is a method for engaging rural and underserved populations, often with strong histories of marginalization, in health research. The Institute of Translational Health Sciences, funded by a National Institutes of Health Clinical...

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Lin CP, Black RA, Laplante J, et al. Facilitating health data sharing across diverse practices and communities. Summit Transl Bioinform. 2010;2010:16-20
Lin, C. P., Black, R. A., Laplante, J., Keppel, G. A., Tuzzio, L., Berg, A. O., Whitener, R. J., Buchwald, D. S., Baldwin, L. M., Fishman, P. A., Greene, S. M., Gennari, J. H., Tarczy-Hornoch, P., & Stephens, K. A. (2010). Facilitating health data sharing across diverse practices and communities. Summit on translational bioinformatics, 201016-20.
Lin, Ching-Ping, et al. "Facilitating health data sharing across diverse practices and communities." Summit on translational bioinformatics vol. 2010 (2010): 16-20.
Lin CP, Black RA, Laplante J, Keppel GA, Tuzzio L, Berg AO, Whitener RJ, Buchwald DS, Baldwin LM, Fishman PA, Greene SM, Gennari JH, Tarczy-Hornoch P, Stephens KA. Facilitating health data sharing across diverse practices and communities. Summit Transl Bioinform. 2010 Mar 01;2010:16-20. PMID: 21347138; PMCID: PMC3041543.
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An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides.

Tetrahedron

Fors BP, Dooleweerdt K, Zeng Q, Buchwald SL.
PMID: 20740063
Tetrahedron. 2009 Aug 15;65(33):6576-6583. doi: 10.1016/j.tet.2009.04.096.

A catalyst based on a new biarylphosphine ligand (3) for the Pd-catalyzed cross-coupling reactions of amides and aryl chlorides is described. This system shows the highest turnover frequencies reported to date for these reactions, especially for aryl chloride substrates...

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Fors BP, Dooleweerdt K, Zeng Q, et al. An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides. Tetrahedron. 2009;65(33):6576-6583doi: 10.1016/j.tet.2009.04.096.
Fors, B. P., Dooleweerdt, K., Zeng, Q., & Buchwald, S. L. (2009). An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides. Tetrahedron, 65(33), 6576-6583. https://doi.org/10.1016/j.tet.2009.04.096
Fors, Brett P, et al. "An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides." Tetrahedron vol. 65,33 (2009): 6576-6583. doi: https://doi.org/10.1016/j.tet.2009.04.096
Fors BP, Dooleweerdt K, Zeng Q, Buchwald SL. An Efficient System For the Pd-Catalyzed Cross-Coupling of Amides and Aryl Chlorides. Tetrahedron. 2009 Aug 15;65(33):6576-6583. doi: 10.1016/j.tet.2009.04.096. PMID: 20740063; PMCID: PMC2927134.
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Si/Ge junctions formed by nanomembrane bonding.

ACS nano

Kiefer AM, Paskiewicz DM, Clausen AM, Buchwald WR, Soref RA, Lagally MG.
PMID: 21247201
ACS Nano. 2011 Feb 22;5(2):1179-89. doi: 10.1021/nn103149c. Epub 2011 Jan 19.

We demonstrate the feasibility of fabricating heterojunctions of semiconductors with high mismatches in lattice constant and coefficient of thermal expansion by employing nanomembrane bonding. We investigate the structure of and electrical transport across the interface of a Si/Ge bilayer...

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Kiefer AM, Paskiewicz DM, Clausen AM, et al. Si/Ge junctions formed by nanomembrane bonding. ACS Nano. 2011;5(2):1179-89doi: 10.1021/nn103149c.
Kiefer, A. M., Paskiewicz, D. M., Clausen, A. M., Buchwald, W. R., Soref, R. A., & Lagally, M. G. (2011). Si/Ge junctions formed by nanomembrane bonding. ACS nano, 5(2), 1179-89. https://doi.org/10.1021/nn103149c
Kiefer, Arnold M, et al. "Si/Ge junctions formed by nanomembrane bonding." ACS nano vol. 5,2 (2011): 1179-89. doi: https://doi.org/10.1021/nn103149c
Kiefer AM, Paskiewicz DM, Clausen AM, Buchwald WR, Soref RA, Lagally MG. Si/Ge junctions formed by nanomembrane bonding. ACS Nano. 2011 Feb 22;5(2):1179-89. doi: 10.1021/nn103149c. Epub 2011 Jan 19. PMID: 21247201.
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Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.

Chemical science

Surry DS, Buchwald SL.
PMID: 22432049
Chem Sci. 2011;2(1):27-50. doi: 10.1039/C0SC00331J.

Dialkylbiaryl phosphines are a valuable class of ligand for Pd-catalyzed amination reactions and have been applied in a range of contexts. This review attempts to aid the reader in the selection of the best choice of reaction conditions and...

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Surry DS, Buchwald SL. Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide. Chem Sci. 2011;2(1):27-50doi: 10.1039/C0SC00331J.
Surry, D. S., & Buchwald, S. L. (2011). Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide. Chemical science, 2(1), 27-50. https://doi.org/10.1039/C0SC00331J
Surry, David S, and Buchwald, Stephen L. "Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide." Chemical science vol. 2,1 (2011): 27-50. doi: https://doi.org/10.1039/C0SC00331J
Surry DS, Buchwald SL. Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide. Chem Sci. 2011;2(1):27-50. doi: 10.1039/C0SC00331J. PMID: 22432049; PMCID: PMC3306613.
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Journals under threat. A joint response from History of Science, Technology and Medicine editors.

Studium (Rotterdam, Netherlands)

Fox R, Andersen H, Ariew R, Feingold M, Bag AK, Barrow-Green J, van Dalen B, Benson K, Beretta M, Blay M, Borck C, Bowker G, Star SL, Bucciantini M, Camerota M, Buchwald J, Gray J, Cappelletti V, Cimino G, Clark M, Keller A, Cline R, Clucas S, Gaukroger S, Cook H, Hardy A, Corry L, Métraux A, Renn J, Dolan B, Luckin B, Duerbeck H, Orchiston W, Epple M, Hård M, Rheinberger HJ, Roelcke V, French S, Farber P, Fissell M, Packard R, Good J, Hackmann W, Halleux R, Holmqvist B, Hoskin M, Inkster I, Spada MF, Jardine N, Levere T, Lightman B, Lüthy C, Lynch M, McCluskey S, Ruggles C, Morris P, Nelson EC, Nicholson I, Olesko K, Peréz L, Morus IR, Rigden J, Stuewer RH, Samsó J, Schaffer S, Schappacher N, Strom C, Unschuld P, Weingart P, Zamecki S, Zuidervaart H.
PMID: 22586774
Studium (Rotterdam). 2009;2(1):1-3.

No abstract available.

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Fox R, Andersen H, Ariew R, et al. Journals under threat. A joint response from History of Science, Technology and Medicine editors. Studium (Rotterdam). 2009;2(1):1-3
Fox, R., Andersen, H., Ariew, R., Feingold, M., Bag, A. K., Barrow-Green, J., van Dalen, B., Benson, K., Beretta, M., Blay, M., Borck, C., Bowker, G., Star, S. L., Bucciantini, M., Camerota, M., Buchwald, J., Gray, J., Cappelletti, V., Cimino, G., Clark, M., Keller, A., Cline, R., Clucas, S., Gaukroger, S., Cook, H., Hardy, A., Corry, L., Métraux, A., Renn, J., Dolan, B., Luckin, B., Duerbeck, H., Orchiston, W., Epple, M., Hård, M., Rheinberger, H. J., Roelcke, V., French, S., Farber, P., Fissell, M., Packard, R., Good, J., Hackmann, W., Halleux, R., Holmqvist, B., Hoskin, M., Inkster, I., Spada, M. F., Jardine, N., Levere, T., Lightman, B., Lüthy, C., Lynch, M., McCluskey, S., Ruggles, C., Morris, P., Nelson, E. C., Nicholson, I., Olesko, K., Peréz, L., Morus, I. R., Rigden, J., Stuewer, R. H., Samsó, J., Schaffer, S., Schappacher, N., Strom, C., Unschuld, P., Weingart, P., Zamecki, S., & Zuidervaart, H. (2009). Journals under threat. A joint response from History of Science, Technology and Medicine editors. Studium (Rotterdam, Netherlands), 2(1), 1-3.
Fox, Robert, et al. "Journals under threat. A joint response from History of Science, Technology and Medicine editors." Studium (Rotterdam, Netherlands) vol. 2,1 (2009): 1-3.
Fox R, Andersen H, Ariew R, Feingold M, Bag AK, Barrow-Green J, van Dalen B, Benson K, Beretta M, Blay M, Borck C, Bowker G, Star SL, Bucciantini M, Camerota M, Buchwald J, Gray J, Cappelletti V, Cimino G, Clark M, Keller A, Cline R, Clucas S, Gaukroger S, Cook H, Hardy A, Corry L, Métraux A, Renn J, Dolan B, Luckin B, Duerbeck H, Orchiston W, Epple M, Hård M, Rheinberger HJ, Roelcke V, French S, Farber P, Fissell M, Packard R, Good J, Hackmann W, Halleux R, Holmqvist B, Hoskin M, Inkster I, Spada MF, Jardine N, Levere T, Lightman B, Lüthy C, Lynch M, McCluskey S, Ruggles C, Morris P, Nelson EC, Nicholson I, Olesko K, Peréz L, Morus IR, Rigden J, Stuewer RH, Samsó J, Schaffer S, Schappacher N, Strom C, Unschuld P, Weingart P, Zamecki S, Zuidervaart H. Journals under threat. A joint response from History of Science, Technology and Medicine editors. Studium (Rotterdam). 2009;2(1):1-3. PMID: 22586774.
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Collaborative development of predictive toxicology applications.

Journal of cheminformatics

Hardy B, Douglas N, Helma C, Rautenberg M, Jeliazkova N, Jeliazkov V, Nikolova I, Benigni R, Tcheremenskaia O, Kramer S, Girschick T, Buchwald F, Wicker J, Karwath A, Gütlein M, Maunz A, Sarimveis H, Melagraki G, Afantitis A, Sopasakis P, Gallagher D, Poroikov V, Filimonov D, Zakharov A, Lagunin A, Gloriozova T, Novikov S, Skvortsova N, Druzhilovsky D, Chawla S, Ghosh I, Ray S, Patel H, Escher S.
PMID: 20807436
J Cheminform. 2010 Aug 31;2(1):7. doi: 10.1186/1758-2946-2-7.

OpenTox provides an interoperable, standards-based Framework for the support of predictive toxicology data management, algorithms, modelling, validation and reporting. It is relevant to satisfying the chemical safety assessment requirements of the REACH legislation as it supports access to experimental...

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Hardy B, Douglas N, Helma C, et al. Collaborative development of predictive toxicology applications. J Cheminform. 2010;2(1):7doi: 10.1186/1758-2946-2-7.
Hardy, B., Douglas, N., Helma, C., Rautenberg, M., Jeliazkova, N., Jeliazkov, V., Nikolova, I., Benigni, R., Tcheremenskaia, O., Kramer, S., Girschick, T., Buchwald, F., Wicker, J., Karwath, A., Gütlein, M., Maunz, A., Sarimveis, H., Melagraki, G., Afantitis, A., Sopasakis, P., Gallagher, D., Poroikov, V., Filimonov, D., Zakharov, A., Lagunin, A., Gloriozova, T., Novikov, S., Skvortsova, N., Druzhilovsky, D., Chawla, S., Ghosh, I., Ray, S., Patel, H., & Escher, S. (2010). Collaborative development of predictive toxicology applications. Journal of cheminformatics, 2(1), 7. https://doi.org/10.1186/1758-2946-2-7
Hardy, Barry, et al. "Collaborative development of predictive toxicology applications." Journal of cheminformatics vol. 2,1 (2010): 7. doi: https://doi.org/10.1186/1758-2946-2-7
Hardy B, Douglas N, Helma C, Rautenberg M, Jeliazkova N, Jeliazkov V, Nikolova I, Benigni R, Tcheremenskaia O, Kramer S, Girschick T, Buchwald F, Wicker J, Karwath A, Gütlein M, Maunz A, Sarimveis H, Melagraki G, Afantitis A, Sopasakis P, Gallagher D, Poroikov V, Filimonov D, Zakharov A, Lagunin A, Gloriozova T, Novikov S, Skvortsova N, Druzhilovsky D, Chawla S, Ghosh I, Ray S, Patel H, Escher S. Collaborative development of predictive toxicology applications. J Cheminform. 2010 Aug 31;2(1):7. doi: 10.1186/1758-2946-2-7. PMID: 20807436; PMCID: PMC2941473.
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Control of the transition temperatures of metallomesogens by specific interface design: application to Mn12 single molecule magnets.

Dalton transactions (Cambridge, England : 2003)

Terazzi E, Jensen TB, Donnio B, Buchwalder K, Bourgogne C, Rogez G, Heinrich B, Gallani J, Piguet C.
PMID: 21858343
Dalton Trans. 2011 Dec 07;40(45):12028-32. doi: 10.1039/c1dt10908a. Epub 2011 Aug 22.

Reaction of the Single Molecule Magnet [Mn(12)O(12)(CH(3)CO(2))(16)(H(2)O)(4)] (Mn(12)) with mesogenic dendritic ligands Li (i = 4, 5) quantitatively yields functional clusters [Mn(12)O(12)(Li-H)(16)(H(2)O)(4)] (i = 4, 5) that self-organize into a thermotropic SmA-type liquid crystalline phase. The perturbation of the...

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Terazzi E, Jensen TB, Donnio B, et al. Control of the transition temperatures of metallomesogens by specific interface design: application to Mn12 single molecule magnets. Dalton Trans. 2011;40(45):12028-32doi: 10.1039/c1dt10908a.
Terazzi, E., Jensen, T. B., Donnio, B., Buchwalder, K., Bourgogne, C., Rogez, G., Heinrich, B., Gallani, J., & Piguet, C. (2011). Control of the transition temperatures of metallomesogens by specific interface design: application to Mn12 single molecule magnets. Dalton transactions (Cambridge, England : 2003), 40(45), 12028-32. https://doi.org/10.1039/c1dt10908a
Terazzi, E, et al. "Control of the transition temperatures of metallomesogens by specific interface design: application to Mn12 single molecule magnets." Dalton transactions (Cambridge, England : 2003) vol. 40,45 (2011): 12028-32. doi: https://doi.org/10.1039/c1dt10908a
Terazzi E, Jensen TB, Donnio B, Buchwalder K, Bourgogne C, Rogez G, Heinrich B, Gallani J, Piguet C. Control of the transition temperatures of metallomesogens by specific interface design: application to Mn12 single molecule magnets. Dalton Trans. 2011 Dec 07;40(45):12028-32. doi: 10.1039/c1dt10908a. Epub 2011 Aug 22. PMID: 21858343.
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LC Data QUEST: A Technical Architecture for Community Federated Clinical Data Sharing.

AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science

Stephens KA, Lin CP, Baldwin LM, Echo-Hawk A, Keppel GA, Buchwald D, Whitener RJ, Korngiebel DM, Berg AO, Black RA, Tarczy-Hornoch P.
PMID: 22779052
AMIA Jt Summits Transl Sci Proc. 2012;2012:57-62. Epub 2012 Mar 19.

The University of Washington Institute of Translational Health Sciences is engaged in a project, LC Data QUEST, building data sharing capacity in primary care practices serving rural and tribal populations in the Washington, Wyoming, Alaska, Montana, Idaho region to...

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Stephens KA, Lin CP, Baldwin LM, et al. LC Data QUEST: A Technical Architecture for Community Federated Clinical Data Sharing. AMIA Jt Summits Transl Sci Proc. 2012;2012:57-62
Stephens, K. A., Lin, C. P., Baldwin, L. M., Echo-Hawk, A., Keppel, G. A., Buchwald, D., Whitener, R. J., Korngiebel, D. M., Berg, A. O., Black, R. A., & Tarczy-Hornoch, P. (2012). LC Data QUEST: A Technical Architecture for Community Federated Clinical Data Sharing. AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science, 201257-62.
Stephens, Kari A, et al. "LC Data QUEST: A Technical Architecture for Community Federated Clinical Data Sharing." AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science vol. 2012 (2012): 57-62.
Stephens KA, Lin CP, Baldwin LM, Echo-Hawk A, Keppel GA, Buchwald D, Whitener RJ, Korngiebel DM, Berg AO, Black RA, Tarczy-Hornoch P. LC Data QUEST: A Technical Architecture for Community Federated Clinical Data Sharing. AMIA Jt Summits Transl Sci Proc. 2012;2012:57-62. Epub 2012 Mar 19. PMID: 22779052; PMCID: PMC3392065.
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Correction to "A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes".

Journal of the American Chemical Society

Tsai EY, Liu RY, Yang Y, Buchwald SL.
PMID: 29737849
J Am Chem Soc. 2018 May 16;140(19):6184. doi: 10.1021/jacs.8b04366. Epub 2018 May 08.

No abstract available.

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Tsai EY, Liu RY, Yang Y, et al. Correction to "A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes". J Am Chem Soc. 2018;140(19):6184doi: 10.1021/jacs.8b04366.
Tsai, E. Y., Liu, R. Y., Yang, Y., & Buchwald, S. L. (2018). Correction to "A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes". Journal of the American Chemical Society, 140(19), 6184. https://doi.org/10.1021/jacs.8b04366
Tsai, Erica Y, et al. "Correction to "A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes"." Journal of the American Chemical Society vol. 140,19 (2018): 6184. doi: https://doi.org/10.1021/jacs.8b04366
Tsai EY, Liu RY, Yang Y, Buchwald SL. Correction to "A Regio- and Enantioselective CuH-Catalyzed Ketone Allylation with Terminal Allenes". J Am Chem Soc. 2018 May 16;140(19):6184. doi: 10.1021/jacs.8b04366. Epub 2018 May 08. PMID: 29737849.
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Neoadjuvant therapy of locally/regionally advanced melanoma.

Therapeutic advances in medical oncology

Khunger A, Buchwald ZS, Lowe M, Khan MK, Delman KA, Tarhini AA.
PMID: 31391869
Ther Adv Med Oncol. 2019 Jul 31;11:1758835919866959. doi: 10.1177/1758835919866959. eCollection 2019.

Locally/regionally advanced melanoma confers a major challenge in terms of surgical and medical management. Surgical treatment carries the risks of surgical morbidities and potential complications that could be lasting. In addition, these patients continue to have a high risk...

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Khunger A, Buchwald ZS, Lowe M, et al. Neoadjuvant therapy of locally/regionally advanced melanoma. Ther Adv Med Oncol. 2019;11:1758835919866959doi: 10.1177/1758835919866959.
Khunger, A., Buchwald, Z. S., Lowe, M., Khan, M. K., Delman, K. A., & Tarhini, A. A. (2019). Neoadjuvant therapy of locally/regionally advanced melanoma. Therapeutic advances in medical oncology, 111758835919866959. https://doi.org/10.1177/1758835919866959
Khunger, Arjun, et al. "Neoadjuvant therapy of locally/regionally advanced melanoma." Therapeutic advances in medical oncology vol. 11 (2019): 1758835919866959. doi: https://doi.org/10.1177/1758835919866959
Khunger A, Buchwald ZS, Lowe M, Khan MK, Delman KA, Tarhini AA. Neoadjuvant therapy of locally/regionally advanced melanoma. Ther Adv Med Oncol. 2019 Jul 31;11:1758835919866959. doi: 10.1177/1758835919866959. eCollection 2019. PMID: 31391869; PMCID: PMC6669845.
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Copper-Catalyzed Enantioselective Hydroamination of Alkenes.

Organic syntheses; an annual publication of satisfactory methods for the preparation of organic chemicals

Liu RY, Buchwald SL.
PMID: 30287975
Organic Synth. 2018;95:80-96. doi: 10.15227/orgsyn.095.0080.

No abstract available.

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Liu RY, Buchwald SL. Copper-Catalyzed Enantioselective Hydroamination of Alkenes. Organic Synth. 2018;95:80-96doi: 10.15227/orgsyn.095.0080.
Liu, R. Y., & Buchwald, S. L. (2018). Copper-Catalyzed Enantioselective Hydroamination of Alkenes. Organic syntheses; an annual publication of satisfactory methods for the preparation of organic chemicals, 9580-96. https://doi.org/10.15227/orgsyn.095.0080
Liu, Richard Y, and Buchwald, Stephen L. "Copper-Catalyzed Enantioselective Hydroamination of Alkenes." Organic syntheses; an annual publication of satisfactory methods for the preparation of organic chemicals vol. 95 (2018): 80-96. doi: https://doi.org/10.15227/orgsyn.095.0080
Liu RY, Buchwald SL. Copper-Catalyzed Enantioselective Hydroamination of Alkenes. Organic Synth. 2018;95:80-96. doi: 10.15227/orgsyn.095.0080. PMID: 30287975; PMCID: PMC6168011.
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Growth of vertically aligned nanowires in metal-oxide nanocomposites: kinetic Monte-Carlo modeling versus experiments.

Nanoscale

Hennes M, Schuler V, Weng X, Buchwald J, Demaille D, Zheng Y, Vidal F.
PMID: 29651470
Nanoscale. 2018 Apr 26;10(16):7666-7675. doi: 10.1039/c7nr08974k.

We employ kinetic Monte-Carlo simulations to study the growth process of metal-oxide nanocomposites obtained via sequential pulsed laser deposition. Using Ni-SrTiO3 (Ni-STO) as a model system, we reduce the complexity of the computational problem by choosing a coarse-grained approach...

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Hennes M, Schuler V, Weng X, et al. Growth of vertically aligned nanowires in metal-oxide nanocomposites: kinetic Monte-Carlo modeling versus experiments. Nanoscale. 2018;10(16):7666-7675doi: 10.1039/c7nr08974k.
Hennes, M., Schuler, V., Weng, X., Buchwald, J., Demaille, D., Zheng, Y., & Vidal, F. (2018). Growth of vertically aligned nanowires in metal-oxide nanocomposites: kinetic Monte-Carlo modeling versus experiments. Nanoscale, 10(16), 7666-7675. https://doi.org/10.1039/c7nr08974k
Hennes, M, et al. "Growth of vertically aligned nanowires in metal-oxide nanocomposites: kinetic Monte-Carlo modeling versus experiments." Nanoscale vol. 10,16 (2018): 7666-7675. doi: https://doi.org/10.1039/c7nr08974k
Hennes M, Schuler V, Weng X, Buchwald J, Demaille D, Zheng Y, Vidal F. Growth of vertically aligned nanowires in metal-oxide nanocomposites: kinetic Monte-Carlo modeling versus experiments. Nanoscale. 2018 Apr 26;10(16):7666-7675. doi: 10.1039/c7nr08974k. PMID: 29651470.
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