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/vufind/Search/Results?lookfor=%22Bernstein%2C+Jonathan+A%22&type=Person&sort=year
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PubPharm (975)
1
The Definition, Acronyms, Nomenclature, and Classification of Angioedema : AAAAI, ACAAI, ACARE, and APAACI DANCE Consensus
enthalten in:
The Journal of allergy and clinical immunology
| 2024
von
Reshef, A.
|
Buttgereit, T.
|
Betschel, S.
| +90
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2
InpherNet provides attractive monogenic disease gene hypotheses using patient genes indirect neighbors
enthalten in:
bioRxiv.org
| 2024
von
Yoo, B.
|
Birgmeier, J.
|
Bernstein, J.
| +1
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3
DPP9 deficiency: an Inflammasomopathy which can be rescued by lowering NLRP1/IL-1 signaling
enthalten in:
bioRxiv.org
| 2024
von
Harapas, C.
|
Robinson, K.
|
Lay, K.
| +18
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4
A cross-sectional study of the neuropsychiatric phenotype of
CACNA1C
-related disorder
enthalten in:
bioRxiv.org
| 2024
von
Levy, R.
|
Timothy, K.
|
Underwood, J.
| +3
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5
Large deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome
enthalten in:
bioRxiv.org
| 2024
von
Breen, M.
|
Fan, X.
|
Levy, T.
| +12
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6
Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism
enthalten in:
Annals of clinical and translational neurology
| 2024
von
Dohrn, M.
|
Bademci, G.
|
Rebelo, A.
| +110
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7
Efficacy and Safety of Systemic Corticosteroids for Urticaria : A systematic review and meta-analysis of randomized clinical trials
enthalten in:
The journal of allergy and clinical immunology. In practice
| 2024
von
Chu, X.
|
Wang, J.
|
Ologundudu, L.
| +26
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8
Filamin A heart valve disease as a genetic cause of inherited bicuspid and tricuspid aortic valve disease
enthalten in:
Heart (British Cardiac Society)
| 2024
von
Delwarde, C.
|
Toquet, C.
|
Boureau, A.
| +12
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9
Immunological and hematological findings as major features in a patient with a new germline pathogenic CBL variant
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Stellacci, E.
|
Carter, J.
|
Pannone, L.
| +7
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10
De novo
variants in the non-coding spliceosomal snRNA gene
RNU4-2
are a frequent cause of syndromic neurodevelopmental disorders
enthalten in:
bioRxiv.org
| 2024
von
Chen, Y.
|
Dawes, R.
|
Kim, H.
| +94
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Annals of allergy, asthma & immunology : offici...
57
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55
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54
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40
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32
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23
Genetics in medicine : official journal of the ...
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Journal of genetic counseling
20
bioRxiv.org
18
Immunology and allergy clinics of North America
18
The Journal of asthma : official journal of the...
18
The World Allergy Organization journal
13
The New England journal of medicine
10
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10
Human mutation
10
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530
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224
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136
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116
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62
Complement C1 Inhibitor Protein
61
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45
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41
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41
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29
Asthma
27
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24
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24
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23
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22
Clinical Trial, Phase III
20
2P471X1Z11
20
Bradykinin
19
Immunoglobulin E
18
37341-29-0
18
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