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Cazin, Caroline
170  results:
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1

Whole genome sequencing identifies a homozygous splicing va..:

Amiri‐Yekta, Amir ; Sen, Sharanya ; Hazane‐Puch, Florence...
Clinical Genetics.  , 2024
Link: https://doi.org/10.1111/..
 
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2

Lack of CCDC146, a ubiquitous centriole and microtubule-ass..:

Kherraf, Zine Eddine ; Muroňová, Jana ; Giordani, Elsa...
eLife.  12 (2024)  - p. , 2024
Link: https://doi.org/10.7554/..
 
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3

Lack of CCDC146, a ubiquitous centriole and microtubule-ass..:

Kherraf, Zine Eddine ; Muroňová, Jana ; Giordani, Elsa...
eLife.  12 (2024)  - p. , 2024
Link: https://doi.org/10.7554/..
 
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4

CCDC65, encoding a component of the axonemal Nexin‐Dynein r..:

Jreijiri, Fadwa ; Cavarocchi, Emma ; Amiri‐Yekta, Amir...
Clinical Genetics.  , 2023
Link: https://doi.org/10.1111/..
 
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5

Identification of IQCH as a calmodulin-associated protein r..:

Cavarocchi, Emma ; Sayou, Camille ; Lorès, Patrick...
iScience.  26 (2023)  8 - p. 107354 , 2023
Link: https://doi.org/10.1016/..
 
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6

A splice donor variant of GAS8 induces structural disorgani..:

Kherraf, Zine‐Eddine ; Barbotin, Anne‐Laure ; Martinez, Guillaume...
Clinical Genetics.  105 (2023)  2 - p. 220-225 , 2023
Link: https://doi.org/10.1111/..
 
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7

Novel axonemal protein ZMYND12 interacts with TTC29 and DNA..:

Martinez, Guillaume ; Dacheux, Denis ; Broster Reix, Christine E...
eLife.  12 (2023)  - p. , 2023
Link: https://doi.org/10.7554/..
 
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8

Expanding the sperm phenotype caused by mutations in SPATA2..:

Martinez, Guillaume ; Metzler‐Guillemain, Catherine ; Cazin, Caroline...
Clinical Genetics.  103 (2023)  5 - p. 612-614 , 2023
Link: https://doi.org/10.1111/..
 
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9

New Mutations in DNHD1 Cause Multiple Morphological Abnorma..:

Martinez, Guillaume ; Barbotin, Anne-Laure ; Cazin, Caroline...
International Journal of Molecular Sciences.  24 (2023)  3 - p. 2559 , 2023
Link: https://doi.org/10.3390/..
 
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10

Novel axonemal protein ZMYND12 interacts with TTC29 and DNA..:

Martinez, Guillaume ; Dacheux, Denis ; Broster Reix, Christine E...
eLife.  12 (2023)  - p. , 2023
Link: https://doi.org/10.7554/..
 
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11

Genetic causes of macrozoospermia and proposal for an optim..:

Coudert, Alicia ; Cazin, Caroline ; Amiri-Yekta, Amir...
Journal of Genetics and Genomics.  50 (2023)  7 - p. 536-540 , 2023
Link: https://doi.org/10.1016/..
 
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12

Oligogenic heterozygous inheritance of sperm abnormalities ..:

Martinez, Guillaume ; Coutton, Charles ; Loeuillet, Corinne...
eLife.  11 (2022)  - p. , 2022
Link: https://doi.org/10.7554/..
 
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13

A recurrent ZP1 variant is responsible for oocyte maturatio..:

Loeuillet, Corinne ; Dhellemmes, Magali ; Cazin, Caroline...
Clinical Genetics.  102 (2022)  1 - p. 22-29 , 2022
Link: https://doi.org/10.1111/..
 
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14

Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to S..:

Cazin, Caroline ; Neirijnck, Yasmine ; Loeuillet, Corinne...
Cells.  11 (2021)  1 - p. 118 , 2021
Link: https://doi.org/10.3390/..
 
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15

Correction to: A missense mutation in IFT74, encoding for a..:

Lorès, Patrick ; Kherraf, Zine-Eddine ; Amiri-Yekta, Amir...
Human Genetics.  140 (2021)  7 - p. 1045-1045 , 2021
Link: https://doi.org/10.1007/..
 
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