Joseph Buxbaum (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Joseph Buxbaum" in English language version.

refsWebsite

Global rank English rank

52nih.gov

4^th place

27doi.org

2^nd place

27worldcat.org

5^th place

9harvard.edu

18^th place

17^th place

2mssm.edu

low place

2inserm.fr

9,568^th place

low place

1mountsinai.org

low place

1scholar.google.com

1,697^th place

1,040^th place

1web.archive.org

1^st place

1mhnews-autism.org

low place

1nam.edu

low place

doi.org (Global: 2^nd place; English: 2^nd place)

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret; Buxbaum, Joseph D. (2012-02-01). "Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease". Neurobiology of Aging. 33 (2): 416–417.e3. doi:10.1016/j.neurobiolaging.2010.03.003. ISSN 1558-1497. PMC 4084881. PMID 20381196.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J.; Greengard, P. (1990-08-01). "Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation". Proceedings of the National Academy of Sciences of the United States of America. 87 (15): 6003–6006. Bibcode:1990PNAS...87.6003B. doi:10.1073/pnas.87.15.6003. ISSN 0027-8424. PMC 54458. PMID 2116015.
Buxbaum, J. D.; Liu, K. N.; Luo, Y.; Slack, J. L.; Stocking, K. L.; Peschon, J. J.; Johnson, R. S.; Castner, B. J.; Cerretti, D. P. (1998-10-23). "Evidence that tumor necrosis factor alpha converting enzyme is involved in regulated alpha-secretase cleavage of the Alzheimer amyloid protein precursor". The Journal of Biological Chemistry. 273 (43): 27765–27767. doi:10.1074/jbc.273.43.27765. ISSN 0021-9258. PMID 9774383.
Näslund, J.; Haroutunian, V.; Mohs, R.; Davis, K. L.; Davies, P.; Greengard, P.; Buxbaum, J. D. (2000-03-22). "Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline". JAMA. 283 (12): 1571–1577. doi:10.1001/jama.283.12.1571. ISSN 0098-7484. PMID 10735393.
Naj, Adam C.; Beecham, Gary W.; Martin, Eden R.; Gallins, Paul J.; Powell, Eric H.; Konidari, Ioanna; Whitehead, Patrice L.; Cai, Guiqing; Haroutunian, Vahram (2010-09-01). "Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities". PLOS Genetics. 6 (9) e1001130. doi:10.1371/journal.pgen.1001130. ISSN 1553-7404. PMC 2944795. PMID 20885792.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (2001-04-10). "Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 98 (8): 4746–4751. Bibcode:2001PNAS...98.4746H. doi:10.1073/pnas.081071198. ISSN 0027-8424. PMC 31905. PMID 11296301.
Buxbaum, J. D.; Georgieva, L.; Young, J. J.; Plescia, C.; Kajiwara, Y.; Jiang, Y.; Moskvina, V.; Norton, N.; Peirce, T. (2008-02-01). "Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene". Molecular Psychiatry. 13 (2): 162–172. doi:10.1038/sj.mp.4001991. ISSN 1359-4184. PMC 5567789. PMID 17579610.
Takahashi, N.; Sakurai, T.; Bozdagi-Gunal, O.; Dorr, N. P.; Moy, J.; Krug, L.; Gama-Sosa, M.; Elder, G. A.; Koch, R. J. (2011-01-01). "Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes". Translational Psychiatry. 1 (5) e8. doi:10.1038/tp.2011.8. ISSN 2158-3188. PMC 3309478. PMID 22832403.
Weiss, L. A.; Escayg, A.; Kearney, J. A.; Trudeau, M.; MacDonald, B. T.; Mori, M.; Reichert, J.; Buxbaum, J. D.; Meisler, M. H. (2003-02-01). "Sodium channels SCN1A, SCN2A and SCN3A in familial autism". Molecular Psychiatry. 8 (2): 186–194. doi:10.1038/sj.mp.4001241. ISSN 1359-4184. PMID 12610651.
Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Sanders, Stephan J.; He, Xin; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H.; Bishop, Somer L. (2015-09-23). "Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci". Neuron. 87 (6): 1215–1233. doi:10.1016/j.neuron.2015.09.016. ISSN 1097-4199. PMC 4624267. PMID 26402605.
Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Lehner, Thomas; Roeder, Kathryn; State, Matthew W.; Autism Sequencing Consortium (2012-12-20). "The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders". Neuron. 76 (6): 1052–1056. doi:10.1016/j.neuron.2012.12.008. ISSN 1097-4199. PMC 3863639. PMID 23259942.
Bozdagi, Ozlem; Sakurai, Takeshi; Papapetrou, Danae; Wang, Xiaobin; Dickstein, Dara L.; Takahashi, Nagahide; Kajiwara, Yuji; Yang, Mu; Katz, Adam M. (2010-01-01). "Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication". Molecular Autism. 1 (1): 15. doi:10.1186/2040-2392-1-15. ISSN 2040-2392. PMC 3019144. PMID 21167025.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita; Sosa, Miguel A. Gama (2005-07-05). "Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene". Proceedings of the National Academy of Sciences of the United States of America. 102 (27): 9643–9648. Bibcode:2005PNAS..102.9643S. doi:10.1073/pnas.0503739102. ISSN 0027-8424. PMC 1160518. PMID 15983371.
Kajiwara, Yuji; Schiff, Tamar; Voloudakis, Georgios; Gama Sosa, Miguel A.; Elder, Gregory; Bozdagi, Ozlem; Buxbaum, Joseph D. (2014-07-01). "A critical role for human caspase-4 in endotoxin sensitivity". Journal of Immunology. 193 (1): 335–343. doi:10.4049/jimmunol.1303424. ISSN 1550-6606. PMC 4066208. PMID 24879791.
Kolevzon, Alexander; Bush, Lauren; Wang, A. Ting; Halpern, Danielle; Frank, Yitzchak; Grodberg, David; Rapaport, Robert; Tavassoli, Teresa; Chaplin, William (2014-01-01). "A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome". Molecular Autism. 5 (1): 54. doi:10.1186/2040-2392-5-54. ISSN 2040-2392. PMC 4326443. PMID 25685306.

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J.; Greengard, P. (1990-08-01). "Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation". Proceedings of the National Academy of Sciences of the United States of America. 87 (15): 6003–6006. Bibcode:1990PNAS...87.6003B. doi:10.1073/pnas.87.15.6003. ISSN 0027-8424. PMC 54458. PMID 2116015.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (2001-04-10). "Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 98 (8): 4746–4751. Bibcode:2001PNAS...98.4746H. doi:10.1073/pnas.081071198. ISSN 0027-8424. PMC 31905. PMID 11296301.
Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita; Sosa, Miguel A. Gama (2005-07-05). "Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene". Proceedings of the National Academy of Sciences of the United States of America. 102 (27): 9643–9648. Bibcode:2005PNAS..102.9643S. doi:10.1073/pnas.0503739102. ISSN 0027-8424. PMC 1160518. PMID 15983371.

inserm.fr (Global: 9,568^th place; English: low place)

hal.inserm.fr

Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.

mhnews-autism.org (Global: low place; English: low place)

"ASN 2014 Awards Reception Journal" (PDF). December 4, 2014. Archived from the original (PDF) on September 8, 2015. Retrieved February 9, 2016.

mountsinai.org (Global: low place; English: low place)

"Joseph D Buxbaum - The Mount Sinai Hospital". The Mount Sinai Hospital. Retrieved 2016-01-27.

mssm.edu (Global: low place; English: low place)

icahn.mssm.edu

"Directors | Icahn School of Medicine". Icahn School of Medicine at Mount Sinai. Retrieved 2016-01-25.
"Joseph D Buxbaum - Icahn School of Medicine at Mount Sinai". Icahn School of Medicine at Mount Sinai.

nam.edu (Global: low place; English: low place)

"NAM Elects 80 New Members". 2015-10-19.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret; Buxbaum, Joseph D. (2012-02-01). "Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease". Neurobiology of Aging. 33 (2): 416–417.e3. doi:10.1016/j.neurobiolaging.2010.03.003. ISSN 1558-1497. PMC 4084881. PMID 20381196.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J.; Greengard, P. (1990-08-01). "Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation". Proceedings of the National Academy of Sciences of the United States of America. 87 (15): 6003–6006. Bibcode:1990PNAS...87.6003B. doi:10.1073/pnas.87.15.6003. ISSN 0027-8424. PMC 54458. PMID 2116015.
Buxbaum, J. D.; Liu, K. N.; Luo, Y.; Slack, J. L.; Stocking, K. L.; Peschon, J. J.; Johnson, R. S.; Castner, B. J.; Cerretti, D. P. (1998-10-23). "Evidence that tumor necrosis factor alpha converting enzyme is involved in regulated alpha-secretase cleavage of the Alzheimer amyloid protein precursor". The Journal of Biological Chemistry. 273 (43): 27765–27767. doi:10.1074/jbc.273.43.27765. ISSN 0021-9258. PMID 9774383.
Näslund, J.; Haroutunian, V.; Mohs, R.; Davis, K. L.; Davies, P.; Greengard, P.; Buxbaum, J. D. (2000-03-22). "Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline". JAMA. 283 (12): 1571–1577. doi:10.1001/jama.283.12.1571. ISSN 0098-7484. PMID 10735393.
Naj, Adam C.; Beecham, Gary W.; Martin, Eden R.; Gallins, Paul J.; Powell, Eric H.; Konidari, Ioanna; Whitehead, Patrice L.; Cai, Guiqing; Haroutunian, Vahram (2010-09-01). "Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities". PLOS Genetics. 6 (9) e1001130. doi:10.1371/journal.pgen.1001130. ISSN 1553-7404. PMC 2944795. PMID 20885792.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (2001-04-10). "Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 98 (8): 4746–4751. Bibcode:2001PNAS...98.4746H. doi:10.1073/pnas.081071198. ISSN 0027-8424. PMC 31905. PMID 11296301.
Buxbaum, J. D.; Georgieva, L.; Young, J. J.; Plescia, C.; Kajiwara, Y.; Jiang, Y.; Moskvina, V.; Norton, N.; Peirce, T. (2008-02-01). "Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene". Molecular Psychiatry. 13 (2): 162–172. doi:10.1038/sj.mp.4001991. ISSN 1359-4184. PMC 5567789. PMID 17579610.
Takahashi, N.; Sakurai, T.; Bozdagi-Gunal, O.; Dorr, N. P.; Moy, J.; Krug, L.; Gama-Sosa, M.; Elder, G. A.; Koch, R. J. (2011-01-01). "Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes". Translational Psychiatry. 1 (5) e8. doi:10.1038/tp.2011.8. ISSN 2158-3188. PMC 3309478. PMID 22832403.
Weiss, L. A.; Escayg, A.; Kearney, J. A.; Trudeau, M.; MacDonald, B. T.; Mori, M.; Reichert, J.; Buxbaum, J. D.; Meisler, M. H. (2003-02-01). "Sodium channels SCN1A, SCN2A and SCN3A in familial autism". Molecular Psychiatry. 8 (2): 186–194. doi:10.1038/sj.mp.4001241. ISSN 1359-4184. PMID 12610651.
Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Sanders, Stephan J.; He, Xin; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H.; Bishop, Somer L. (2015-09-23). "Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci". Neuron. 87 (6): 1215–1233. doi:10.1016/j.neuron.2015.09.016. ISSN 1097-4199. PMC 4624267. PMID 26402605.
Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Lehner, Thomas; Roeder, Kathryn; State, Matthew W.; Autism Sequencing Consortium (2012-12-20). "The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders". Neuron. 76 (6): 1052–1056. doi:10.1016/j.neuron.2012.12.008. ISSN 1097-4199. PMC 3863639. PMID 23259942.
Bozdagi, Ozlem; Sakurai, Takeshi; Papapetrou, Danae; Wang, Xiaobin; Dickstein, Dara L.; Takahashi, Nagahide; Kajiwara, Yuji; Yang, Mu; Katz, Adam M. (2010-01-01). "Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication". Molecular Autism. 1 (1): 15. doi:10.1186/2040-2392-1-15. ISSN 2040-2392. PMC 3019144. PMID 21167025.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita; Sosa, Miguel A. Gama (2005-07-05). "Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene". Proceedings of the National Academy of Sciences of the United States of America. 102 (27): 9643–9648. Bibcode:2005PNAS..102.9643S. doi:10.1073/pnas.0503739102. ISSN 0027-8424. PMC 1160518. PMID 15983371.
Kajiwara, Yuji; Schiff, Tamar; Voloudakis, Georgios; Gama Sosa, Miguel A.; Elder, Gregory; Bozdagi, Ozlem; Buxbaum, Joseph D. (2014-07-01). "A critical role for human caspase-4 in endotoxin sensitivity". Journal of Immunology. 193 (1): 335–343. doi:10.4049/jimmunol.1303424. ISSN 1550-6606. PMC 4066208. PMID 24879791.
Kolevzon, Alexander; Bush, Lauren; Wang, A. Ting; Halpern, Danielle; Frank, Yitzchak; Grodberg, David; Rapaport, Robert; Tavassoli, Teresa; Chaplin, William (2014-01-01). "A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome". Molecular Autism. 5 (1): 54. doi:10.1186/2040-2392-5-54. ISSN 2040-2392. PMC 4326443. PMID 25685306.

ncbi.nlm.nih.gov

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret; Buxbaum, Joseph D. (2012-02-01). "Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease". Neurobiology of Aging. 33 (2): 416–417.e3. doi:10.1016/j.neurobiolaging.2010.03.003. ISSN 1558-1497. PMC 4084881. PMID 20381196.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J.; Greengard, P. (1990-08-01). "Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation". Proceedings of the National Academy of Sciences of the United States of America. 87 (15): 6003–6006. Bibcode:1990PNAS...87.6003B. doi:10.1073/pnas.87.15.6003. ISSN 0027-8424. PMC 54458. PMID 2116015.
Naj, Adam C.; Beecham, Gary W.; Martin, Eden R.; Gallins, Paul J.; Powell, Eric H.; Konidari, Ioanna; Whitehead, Patrice L.; Cai, Guiqing; Haroutunian, Vahram (2010-09-01). "Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities". PLOS Genetics. 6 (9) e1001130. doi:10.1371/journal.pgen.1001130. ISSN 1553-7404. PMC 2944795. PMID 20885792.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (2001-04-10). "Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 98 (8): 4746–4751. Bibcode:2001PNAS...98.4746H. doi:10.1073/pnas.081071198. ISSN 0027-8424. PMC 31905. PMID 11296301.
Buxbaum, J. D.; Georgieva, L.; Young, J. J.; Plescia, C.; Kajiwara, Y.; Jiang, Y.; Moskvina, V.; Norton, N.; Peirce, T. (2008-02-01). "Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene". Molecular Psychiatry. 13 (2): 162–172. doi:10.1038/sj.mp.4001991. ISSN 1359-4184. PMC 5567789. PMID 17579610.
Takahashi, N.; Sakurai, T.; Bozdagi-Gunal, O.; Dorr, N. P.; Moy, J.; Krug, L.; Gama-Sosa, M.; Elder, G. A.; Koch, R. J. (2011-01-01). "Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes". Translational Psychiatry. 1 (5) e8. doi:10.1038/tp.2011.8. ISSN 2158-3188. PMC 3309478. PMID 22832403.
Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Sanders, Stephan J.; He, Xin; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H.; Bishop, Somer L. (2015-09-23). "Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci". Neuron. 87 (6): 1215–1233. doi:10.1016/j.neuron.2015.09.016. ISSN 1097-4199. PMC 4624267. PMID 26402605.
Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Lehner, Thomas; Roeder, Kathryn; State, Matthew W.; Autism Sequencing Consortium (2012-12-20). "The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders". Neuron. 76 (6): 1052–1056. doi:10.1016/j.neuron.2012.12.008. ISSN 1097-4199. PMC 3863639. PMID 23259942.
Bozdagi, Ozlem; Sakurai, Takeshi; Papapetrou, Danae; Wang, Xiaobin; Dickstein, Dara L.; Takahashi, Nagahide; Kajiwara, Yuji; Yang, Mu; Katz, Adam M. (2010-01-01). "Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication". Molecular Autism. 1 (1): 15. doi:10.1186/2040-2392-1-15. ISSN 2040-2392. PMC 3019144. PMID 21167025.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita; Sosa, Miguel A. Gama (2005-07-05). "Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene". Proceedings of the National Academy of Sciences of the United States of America. 102 (27): 9643–9648. Bibcode:2005PNAS..102.9643S. doi:10.1073/pnas.0503739102. ISSN 0027-8424. PMC 1160518. PMID 15983371.
Kajiwara, Yuji; Schiff, Tamar; Voloudakis, Georgios; Gama Sosa, Miguel A.; Elder, Gregory; Bozdagi, Ozlem; Buxbaum, Joseph D. (2014-07-01). "A critical role for human caspase-4 in endotoxin sensitivity". Journal of Immunology. 193 (1): 335–343. doi:10.4049/jimmunol.1303424. ISSN 1550-6606. PMC 4066208. PMID 24879791.
Kolevzon, Alexander; Bush, Lauren; Wang, A. Ting; Halpern, Danielle; Frank, Yitzchak; Grodberg, David; Rapaport, Robert; Tavassoli, Teresa; Chaplin, William (2014-01-01). "A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome". Molecular Autism. 5 (1): 54. doi:10.1186/2040-2392-5-54. ISSN 2040-2392. PMC 4326443. PMID 25685306.
"My Bibliography - My NCBI Collection". www.ncbi.nlm.nih.gov. Retrieved 2016-02-10.

scholar.google.com (Global: 1,697^th place; English: 1,040^th place)

"Joseph D Buxbaum - Google Scholar Citations". scholar.google.com. Retrieved 2016-02-12.

web.archive.org (Global: 1^st place; English: 1^st place)

"ASN 2014 Awards Reception Journal" (PDF). December 4, 2014. Archived from the original (PDF) on September 8, 2015. Retrieved February 9, 2016.

worldcat.org (Global: 5^th place; English: 5^th place)

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Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret; Buxbaum, Joseph D. (2012-02-01). "Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease". Neurobiology of Aging. 33 (2): 416–417.e3. doi:10.1016/j.neurobiolaging.2010.03.003. ISSN 1558-1497. PMC 4084881. PMID 20381196.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li; Fromer, Menachem (2014-11-13). "Synaptic, transcriptional and chromatin genes disrupted in autism". Nature. 515 (7526): 209–215. Bibcode:2014Natur.515..209.. doi:10.1038/nature13772. ISSN 1476-4687. PMC 4402723. PMID 25363760.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J.; Greengard, P. (1990-08-01). "Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation". Proceedings of the National Academy of Sciences of the United States of America. 87 (15): 6003–6006. Bibcode:1990PNAS...87.6003B. doi:10.1073/pnas.87.15.6003. ISSN 0027-8424. PMC 54458. PMID 2116015.
Buxbaum, J. D.; Liu, K. N.; Luo, Y.; Slack, J. L.; Stocking, K. L.; Peschon, J. J.; Johnson, R. S.; Castner, B. J.; Cerretti, D. P. (1998-10-23). "Evidence that tumor necrosis factor alpha converting enzyme is involved in regulated alpha-secretase cleavage of the Alzheimer amyloid protein precursor". The Journal of Biological Chemistry. 273 (43): 27765–27767. doi:10.1074/jbc.273.43.27765. ISSN 0021-9258. PMID 9774383.
Näslund, J.; Haroutunian, V.; Mohs, R.; Davis, K. L.; Davies, P.; Greengard, P.; Buxbaum, J. D. (2000-03-22). "Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline". JAMA. 283 (12): 1571–1577. doi:10.1001/jama.283.12.1571. ISSN 0098-7484. PMID 10735393.
Naj, Adam C.; Beecham, Gary W.; Martin, Eden R.; Gallins, Paul J.; Powell, Eric H.; Konidari, Ioanna; Whitehead, Patrice L.; Cai, Guiqing; Haroutunian, Vahram (2010-09-01). "Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities". PLOS Genetics. 6 (9) e1001130. doi:10.1371/journal.pgen.1001130. ISSN 1553-7404. PMC 2944795. PMID 20885792.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (2001-04-10). "Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia". Proceedings of the National Academy of Sciences of the United States of America. 98 (8): 4746–4751. Bibcode:2001PNAS...98.4746H. doi:10.1073/pnas.081071198. ISSN 0027-8424. PMC 31905. PMID 11296301.
Buxbaum, J. D.; Georgieva, L.; Young, J. J.; Plescia, C.; Kajiwara, Y.; Jiang, Y.; Moskvina, V.; Norton, N.; Peirce, T. (2008-02-01). "Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene". Molecular Psychiatry. 13 (2): 162–172. doi:10.1038/sj.mp.4001991. ISSN 1359-4184. PMC 5567789. PMID 17579610.
Takahashi, N.; Sakurai, T.; Bozdagi-Gunal, O.; Dorr, N. P.; Moy, J.; Krug, L.; Gama-Sosa, M.; Elder, G. A.; Koch, R. J. (2011-01-01). "Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes". Translational Psychiatry. 1 (5) e8. doi:10.1038/tp.2011.8. ISSN 2158-3188. PMC 3309478. PMID 22832403.
Weiss, L. A.; Escayg, A.; Kearney, J. A.; Trudeau, M.; MacDonald, B. T.; Mori, M.; Reichert, J.; Buxbaum, J. D.; Meisler, M. H. (2003-02-01). "Sodium channels SCN1A, SCN2A and SCN3A in familial autism". Molecular Psychiatry. 8 (2): 186–194. doi:10.1038/sj.mp.4001241. ISSN 1359-4184. PMID 12610651.
Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G.; Lee, Liana (2005-10-11). "Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays". Proceedings of the National Academy of Sciences of the United States of America. 102 (41): 14717–14722. Bibcode:2005PNAS..10214717F. doi:10.1073/pnas.0506677102. ISSN 0027-8424. PMC 1253580. PMID 16203980.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (2008-08-01). "A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders". Autism Research. 1 (4): 251–257. doi:10.1002/aur.30. ISSN 1939-3806. PMC 2678895. PMID 19360675.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San (2012-05-10). "Patterns and rates of exonic de novo mutations in autism spectrum disorders". Nature. 485 (7397): 242–245. Bibcode:2012Natur.485..242N. doi:10.1038/nature11011. ISSN 1476-4687. PMC 3613847. PMID 22495311.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine (2013-10-03). "Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder". American Journal of Human Genetics. 93 (4): 607–619. doi:10.1016/j.ajhg.2013.09.001. ISSN 1537-6605. PMC 3791269. PMID 24094742.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi (2014-08-01). "Most genetic risk for autism resides with common variation". Nature Genetics. 46 (8): 881–885. doi:10.1038/ng.3039. ISSN 1546-1718. PMC 4137411. PMID 25038753.
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