1. A 2.5‐year snapshot of Mendelian discovery. Issue 4 (3rd April 2016) Authors: Solomon, Benjamin D.; Lee, Teresa; Nguyen, Anh‐Dao; Wolfsberg, Tyra G. Journal: Molecular genetics & genomic medicine Issue: Volume 4:Issue 4(2016) Page Start: 392 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Child's HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus. (November 2016) Authors: Cruz, Giovanna I.; Shao, Xiaorong; Quach, Hong; Ho, Kimberly A.; Sterba, Kirsten; Noble, Janelle A.; Patsopoulos, Nikolaos A.; Busch, Michael P.; Triulzi, Darrell J.; Wong, Wendy S.W.; Solomon, Benjamin D.; Niederhuber, John E.; Criswell, Lindsey A.; Barcellos, Lisa F. Journal: Journal of autoimmunity Issue: Volume 74(2016) Page Start: 201 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A Child's HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus. (November 2016) Authors: Cruz, Giovanna I.; Shao, Xiaorong; Quach, Hong; Ho, Kimberly A.; Sterba, Kirsten; Noble, Janelle A.; Patsopoulos, Nikolaos A.; Busch, Michael P.; Triulzi, Darrell J.; Wong, Wendy S.W.; Solomon, Benjamin D.; Niederhuber, John E.; Criswell, Lindsey A.; Barcellos, Lisa F. Journal: Journal of autoimmunity Issue: Volume 74(2016) Page Start: 201 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Analysis of cardiac anomalies in VACTERL association. Issue 12 (December 2013) Authors: Cunningham, Bridget K.; Hadley, Donald W.; Hannoush, Hwaida; Meltzer, Andrew C.; Niforatos, Nickie; Pineda‐Alvarez, Daniel; Sachdev, Vandana; Warren‐Mora, Nicole; Solomon, Benjamin D. Journal: Birth defects research Issue: Volume 97:Issue 12(2013:Dec.) Page Start: 792 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Analysis of renal anomalies in VACTERL association. Issue 10 (5th September 2014) Authors: Cunningham, Bridget K.; Khromykh, Alina; Martinez, Ariel F.; Carney, Tyler; Hadley, Donald W.; Solomon, Benjamin D. Journal: Birth defects research Issue: Volume 100:Issue 10(2014:Oct.) Page Start: 801 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Announcing a new manuscript category for the American Journal of Medical Genetics Part A: Dispatches from Biotech. Issue 9 (23rd July 2020) Authors: Solomon, Benjamin D.; Slavotinek, Anne M. Journal: American journal of medical genetics Issue: Volume 182:Issue 9(2020) Page Start: 2003 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Basan gets a new fingerprint: Mutations in the skin‐specific isoform of SMARCAD1 cause ectodermal dysplasia syndromes with adermatoglyphia. Issue 11 (5th October 2018) Authors: Valentin, Monica N.; Solomon, Benjamin D.; Richard, Gabriele; Ferreira, Carlos R.; Kirkorian, Anna Yasmine Journal: American journal of medical genetics Issue: Volume 176:Issue 11(2018) Page Start: 2451 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Can artificial intelligence save medical genetics?. Issue 2 (11th October 2021) Authors: Solomon, Benjamin D. Journal: American journal of medical genetics Issue: Volume 188:Issue 2(2022) Page Start: 397 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Cancer genetics program: Follow‐up on clinical genetics and genomic medicine in Qatar. Issue 6 (16th December 2018) Authors: Al‐Bader, Salha Bujassoum; Alsulaiman, Reem; Bugrein, Hekmet; Ben Omran, Tawfeg; Abbaszadeh, Fatemeh; Bakheet, Nawal; Apsa Kusasi, Sitti; Abdou, Nema; Solomon, Benjamin D.; Ghazouani, Hafedh Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 6(2018) Page Start: 865 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience. Issue 6 (27th March 2019) Authors: Al‐Dewik, Nader; Mohd, Howaida; Al‐Mureikhi, Mariam; Ali, Rehab; Al‐Mesaifri, Fatma; Mahmoud, Laila; Shahbeck, Noora; El‐Akouri, Karen; Almulla, Mariam; Al Sulaiman, Reem; Musa, Sara; Al‐Marri, Ajayeb Al‐Nabet; Richard, Gabriele; Juusola, Jane; Solomon, Benjamin D.; Alkuraya, Fowzan S.; Ben‐Omran... Journal: American journal of medical genetics Issue: Volume 179:Issue 6(2019) Page Start: 927 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗