PICO Portalanswers from OpenAlex & ORCID
Samuel G. Jacobson
ResearcherPublications, citations & collaboration network
Samuel G. Jacobson is a researcher indexed in PICO Portal from OpenAlex & ORCID.
How many works does Samuel G. Jacobson have?
PICO Portalindexed works
Samuel G. Jacobson has 524 works in the PICO Portal index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Samuel G. Jacobson have?
PICO Portalcitation count
Samuel G. Jacobson has 37,285 citations in the OpenAlex counts PICO Portal stores.
What is the h-index of Samuel G. Jacobson?
PICO Portalh-index
Samuel G. Jacobson has an h-index of 110 in OpenAlex.
What is the i10-index of Samuel G. Jacobson?
PICO Portali10-index
Samuel G. Jacobson has an i10-index of 344 in OpenAlex.
What is the ORCID of Samuel G. Jacobson?
PICO Portalorcid
The ORCID for Samuel G. Jacobson is on the source record.
What is the OpenAlex record for Samuel G. Jacobson?
PICO Portalopenalex
The OpenAlex for Samuel G. Jacobson is on the source record.
What are the most-cited papers on Samuel G. Jacobson?
PICO Portalmost cited works
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
Hemant Khanna, Erica E. Davis, Carlos Murga‐Zamalloa, Alejandro Estrada‐Cuzcano, Irma López, Anneke I. den Hollander, Marijke N. Zonneveld, Mohammad Othman, Naushin Waseem, Christina Chakarova, C. Maubaret, Anna Dı́az-Font, Ian M. MacDonald, Donna M. Muzny, David A. Wheeler, Margaret Morgan, Lora Lewis, Clare V. Logan, Perciliz L. Tan, M Beer, Chris F. Inglehearn, Richard A. Lewis, Samuel G. Jacobson, Carsten Bergmann, Philip L. Beales, Tania Attié‐Bitach, Colin A. Johnson, Edgar A. Otto, Shomi S. Bhattacharya, Friedhelm Hildebrandt, Richard A. Gibbs, Robert K. Koenekoop, Anand Swaroop, Nicholas Katsanis
Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect
Artur V. Cideciyan, Samuel G. Jacobson, Arlene V. Drack, Allen C. Ho, Jason Charng, Alexandra V. Garafalo, Alejandro J. Román, Alexander Sumaroka, Ian C. Han, Maria D. Hochstedler, Wanda Pfeifer, Elliott H. Sohn, Magali Taiel, Michael R. Schwartz, Patricia Biasutto, Wilma de Wit, Michael E. Cheetham, Peter Adamson, David M. Rodman, Gerard Platenburg, Maria D. Tome, Irina Balikova, Fanny Nerinckx, Julie De Zaeytijd, Caroline Van Cauwenbergh, Bart P. Leroy, Stephen R. Russell
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing
Xia Wang, Hui Wang, Vincent Sun, Han-Fang Tuan, Vafa Keser, Keqing Wang, Huanan Ren, Irma López, Jacques Zaneveld, Sorath Noorani Siddiqui, Stephanie Bowles, Ayesha Khan, Jason S. Salvo, Samuel G. Jacobson, Alessandro Iannaccone, Feng Wang, David G. Birch, John R. Heckenlively, Gerald A. Fishman, Elias I. Traboulsi, Yumei Li, Dianna K. Wheaton, Robert K. Koenekoop, Rui Chen
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, Charlotte M. Poloschek, Sabine Defoort‐Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien Dao Luu, Odile Lecompte, Eberhart Zrenner, Marie‐Elise Lancelot, Aline Antonio, Aurore Germain, Christelle Michiels, Claire Audier, Mélanie Letexier, Jean‐Paul Saraiva, Bart P. Leroy, Francis L. Munier, Saddek Mohand‐Saïd, Birgit Lorenz, Christoph Friedburg, Markus N. Preising, Ulrich Kellner, Agnes B. Renner, Veselina Moskova‐Doumanova, Wolfgang Berger, Bernd Wissinger, Christian Hamel, Daniel F. Schorderet, Elfride De Baere, Dror Sharon, Eyal Banin, Samuel G. Jacobson, Dominique Bonneau, Xavier Zanlonghi, Guylène Le Meur, Ingele Casteels, Robert K. Koenekoop, Vernon Long, Françoise Meire, Katrina Prescott, Thomy de Ravel, Ian Simmons, Hoan Nguyen, Hélène Dollfus, Olivier Poch, Thierry Léveillard, Kim T. Nguyen-Ba-Charvet, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz