William W. Hauswirth

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “Prdm1 overexpression causes a photoreceptor fate-shift in nascent, but not mature, bipolar cells”.

Prdm1 overexpression causes a photoreceptor fate-shift in nascent, but not mature, bipolar cells

Developmental Biology(2020)10.1016/j.ydbio.2020.06.003

N/A

0DataRank · unranked

27 citations

Ko U. Park, Jason S. Silver, Vince A. Chiodo, William W. Hauswirth, Joseph A. Brzezinski +1 more

Efficient Transduction of Vascular Endothelial Cells with Recombinant Adeno-Associated Virus Serotype 1 and 5 Vectors

UNC Libraries(2020)10.17615/yqj9-s373

N/A

0DataRank · unranked

2 citations

R. Jude Samulski, Kenneth I. Berns, Kirsten Madsen, C. Craig Tisher, Terence R. Flotte +9 more

Gene Therapy Reforms Photoreceptor Structure and Restores Vision in NPHP5 -associated Leber Congenital Amaurosis

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.07.329821

N/A

0DataRank · unranked

0 citations

Artur V. Cideciyan, Valérie Dufour, Ana Ripolles‐Garcia, Raghavi Sudharsan, Małgorzata Świder +7 more

Retinal angiogenesis suppression through small molecule activation of p53

UNC Libraries(2020)10.17615/acs1-8g23

N/A

0DataRank · unranked

0 citations

Jayakrishna Ambati, Valeria Cicatiello, Laura Tudisco, Nidia Claros, Younghee Kim +10 more

Gene therapy reforms photoreceptor structure and restores vision in NPHP5-associated Leber congenital amaurosis

Molecular Therapy(2021)10.1016/j.ymthe.2021.03.021

N/A

0DataRank · unranked

35 citations

Artur V. Cideciyan, Valérie Dufour, Ana Ripolles‐Garcia, Raghavi Sudharsan, Małgorzata Świder +7 more

CNGB1 ‐related rod‐cone dystrophy: A mutation review and update

Human Mutation(2021)10.1002/humu.24205

N/A

0DataRank · unranked

24 citations

Vasily Smirnov, Cyntia Solis Hernandez, Saddek Mohand‐Saïd, Christel Condroyer, Aline Antonio +28 more

Disease mechanisms of X‐linked cone dystrophy caused by missense mutations in the red and green cone opsins

The FASEB Journal(2021)10.1096/fj.202101066r

N/A

0DataRank · unranked

12 citations

Frank M. Dyka, Xiaojie Ma, Ling Yin, Heather J Yu, Wolfgang Baehr +3 more

Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia

Translational Vision Science & Technology(2021)10.1167/tvst.10.1.11

N/A

0DataRank · unranked

14 citations

Erica N. Woertz, Michalis Georgiou, Emily J Patterson, Byron L. Lam, Gerald A. Fishman +6 more

Development of a translatable gene augmentation therapy for CNGB1-retinitis pigmentosa

Molecular Therapy(2023)10.1016/j.ymthe.2023.04.005

N/A

0DataRank · unranked

14 citations

Lena Zobel, Jonathan Stoddard, Johanna Wagner, Nate Pasmanter, Janice Querubin +15 more