Ngā hua rapu kaituhi

1

Automated validation of genetic variants from large databases: ensuring that variant references refer to the same genomic locations mā Tong, Mark Y., Cassa, Christopher A., Kohane, Isaac S.

I whakaputaina 2011

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2

Re-identification of home addresses from spatial locations anonymized by Gaussian skew mā Cassa, Christopher A, Wieland, Shannon C, Mandl, Kenneth D

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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3

A novel, privacy-preserving cryptographic approach for sharing sequencing data mā Cassa, Christopher A, Miller, Rachel A, Mandl, Kenneth D

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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4

Twitter as a Sentinel in Emergency Situations: Lessons from the Boston Marathon Explosions mā Cassa, Christopher A., Chunara, Rumi, Mandl, Kenneth, Brownstein, John S

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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5

Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals mā Cassa, Christopher A., Tong, Mark Y., Jordan, Daniel M.

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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6

An unsupervised classification method for inferring original case locations from low-resolution disease maps mā Brownstein, John S, Cassa, Christopher A, Kohane, Isaac S, Mandl, Kenneth D

I whakaputaina 2006

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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7

My sister's keeper?: genomic research and the identifiability of siblings mā Cassa, Christopher A, Schmidt, Brian, Kohane, Isaac S, Mandl, Kenneth D

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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8

Mitigating false-positive associations in rare disease gene discovery mā Akle, Sebastian, Chun, Sung, Jordan, Daniel M., Cassa, Christopher A.

I whakaputaina 2015

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9

A literature review at genome scale: improving clinical variant assessment mā Cassa, Christopher A., Jordan, Daniel M., Adzhubei, Ivan, Sunyaev, Shamil

I whakaputaina 2018

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10

A software tool for creating simulated outbreaks to benchmark surveillance systems mā Cassa, Christopher A, Iancu, Karin, Olson, Karen L, Mandl, Kenneth D

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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11

Revealing the spatial distribution of a disease while preserving privacy mā Wieland, Shannon C., Cassa, Christopher A., Mandl, Kenneth D., Berger, Bonnie

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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12

When “N of 2” is not enough: integrating statistical and functional data in gene discovery mā Cassa, Christopher A., Akle, Sebastian, Jordan, Daniel M., Rosenfeld, Jill A.

I whakaputaina 2017

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13

A Context-sensitive Approach to Anonymizing Spatial Surveillance Data: Impact on Outbreak Detection mā Cassa, Christopher A., Grannis, Shaun J., Overhage, J. Marc, Mandl, Kenneth D.

I whakaputaina 2006

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14

Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck mā Balick, Daniel J., Do, Ron, Cassa, Christopher A., Reich, David, Sunyaev, Shamil R.

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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15

Determinants of Base Editing Outcomes from Target Library Analysis and Machine Learning mā Arbab, Mandana, Shen, Max W., Mok, Beverly, Wilson, Christopher, Matuszek, Żaneta, Cassa, Christopher A., Liu, David R.

I whakaputaina 2020

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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16

Disclosing pathogenic genetic variants to research participants: Quantifying an emerging ethical responsibility mā Cassa, Christopher A., Savage, Sarah K., Taylor, Patrick L., Green, Robert C., McGuire, Amy L., Mandl, Kenneth D.

I whakaputaina 2012

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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17

Machine learning based CRISPR gRNA design for therapeutic exon skipping mā Louie, Wilson, Shen, Max W., Tahiry, Zakir, Zhang, Sophia, Worstell, Daniel, Cassa, Christopher A., Sherwood, Richard I., Gifford, David K.

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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18

Identification of cis-suppression of human disease mutations by comparative genomics mā Jordan, Daniel M., Frangakis, Stephan G., Golzio, Christelle, Cassa, Christopher A., Kurtzberg, Joanne, Davis, Erica E., Sunyaev, Shamil R., Katsanis, Nicholas

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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19

Predictable and precise template-free CRISPR editing of pathogenic variants mā Shen, Max W., Arbab, Mandana, Hsu, Jonathan Y., Worstell, Daniel, Culbertson, Sannie J., Krabbe, Olga, Cassa, Christopher A., Liu, David R., Gifford, David K., Sherwood, Richard I.

I whakaputaina 2018

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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20

Estimating the Selective Effects of Heterozygous Protein Truncating Variants from Human Exome Data mā Cassa, Christopher A., Weghorn, Donate, Balick, Daniel J., Jordan, Daniel M., Nusinow, David, Samocha, Kaitlin E., O’Donnell-Luria, Anne, MacArthur, Daniel G., Daly, Mark J., Beier, David R., Sunyaev, Shamil R.

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
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Ngā hua rapu - Cassa, Christopher A

Automated validation of genetic variants from large databases: ensuring that variant references refer to the same genomic locations mā Tong, Mark Y., Cassa, Christopher A., Kohane, Isaac S.

Re-identification of home addresses from spatial locations anonymized by Gaussian skew mā Cassa, Christopher A, Wieland, Shannon C, Mandl, Kenneth D

A novel, privacy-preserving cryptographic approach for sharing sequencing data mā Cassa, Christopher A, Miller, Rachel A, Mandl, Kenneth D

Twitter as a Sentinel in Emergency Situations: Lessons from the Boston Marathon Explosions mā Cassa, Christopher A., Chunara, Rumi, Mandl, Kenneth, Brownstein, John S

Large numbers of genetic variants considered to be pathogenic are common in asymptomatic individuals mā Cassa, Christopher A., Tong, Mark Y., Jordan, Daniel M.

An unsupervised classification method for inferring original case locations from low-resolution disease maps mā Brownstein, John S, Cassa, Christopher A, Kohane, Isaac S, Mandl, Kenneth D

My sister's keeper?: genomic research and the identifiability of siblings mā Cassa, Christopher A, Schmidt, Brian, Kohane, Isaac S, Mandl, Kenneth D

Mitigating false-positive associations in rare disease gene discovery mā Akle, Sebastian, Chun, Sung, Jordan, Daniel M., Cassa, Christopher A.

A literature review at genome scale: improving clinical variant assessment mā Cassa, Christopher A., Jordan, Daniel M., Adzhubei, Ivan, Sunyaev, Shamil

A software tool for creating simulated outbreaks to benchmark surveillance systems mā Cassa, Christopher A, Iancu, Karin, Olson, Karen L, Mandl, Kenneth D

Revealing the spatial distribution of a disease while preserving privacy mā Wieland, Shannon C., Cassa, Christopher A., Mandl, Kenneth D., Berger, Bonnie

When “N of 2” is not enough: integrating statistical and functional data in gene discovery mā Cassa, Christopher A., Akle, Sebastian, Jordan, Daniel M., Rosenfeld, Jill A.

A Context-sensitive Approach to Anonymizing Spatial Surveillance Data: Impact on Outbreak Detection mā Cassa, Christopher A., Grannis, Shaun J., Overhage, J. Marc, Mandl, Kenneth D.

Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck mā Balick, Daniel J., Do, Ron, Cassa, Christopher A., Reich, David, Sunyaev, Shamil R.

Determinants of Base Editing Outcomes from Target Library Analysis and Machine Learning mā Arbab, Mandana, Shen, Max W., Mok, Beverly, Wilson, Christopher, Matuszek, Żaneta, Cassa, Christopher A., Liu, David R.

Disclosing pathogenic genetic variants to research participants: Quantifying an emerging ethical responsibility mā Cassa, Christopher A., Savage, Sarah K., Taylor, Patrick L., Green, Robert C., McGuire, Amy L., Mandl, Kenneth D.

Machine learning based CRISPR gRNA design for therapeutic exon skipping mā Louie, Wilson, Shen, Max W., Tahiry, Zakir, Zhang, Sophia, Worstell, Daniel, Cassa, Christopher A., Sherwood, Richard I., Gifford, David K.

Identification of cis-suppression of human disease mutations by comparative genomics mā Jordan, Daniel M., Frangakis, Stephan G., Golzio, Christelle, Cassa, Christopher A., Kurtzberg, Joanne, Davis, Erica E., Sunyaev, Shamil R., Katsanis, Nicholas

Predictable and precise template-free CRISPR editing of pathogenic variants mā Shen, Max W., Arbab, Mandana, Hsu, Jonathan Y., Worstell, Daniel, Culbertson, Sannie J., Krabbe, Olga, Cassa, Christopher A., Liu, David R., Gifford, David K., Sherwood, Richard I.

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